array:24 [
  "pii" => "S169540330077336X"
  "issn" => "16954033"
  "doi" => "10.1016/S1695-4033(00)77336-X"
  "estado" => "S300"
  "fechaPublicacion" => "2000-03-01"
  "aid" => "77336"
  "copyright" => "Asociación Española de Pediatría"
  "copyrightAnyo" => "2000"
  "documento" => "article"
  "crossmark" => 0
  "subdocumento" => "sco"
  "cita" => "An Pediatr (Barc). 2000;52:267-70"
  "abierto" => array:3 [
    "ES" => false
    "ES2" => false
    "LATM" => false
  ]
  "gratuito" => false
  "lecturas" => array:2 [
    "total" => 5847
    "formatos" => array:3 [
      "EPUB" => 88
      "HTML" => 4745
      "PDF" => 1014
    ]
  ]
  "itemSiguiente" => array:18 [
    "pii" => "S1695403300773371"
    "issn" => "16954033"
    "doi" => "10.1016/S1695-4033(00)77337-1"
    "estado" => "S300"
    "fechaPublicacion" => "2000-03-01"
    "aid" => "77337"
    "copyright" => "Asociación Española de Pediatría"
    "documento" => "article"
    "crossmark" => 0
    "subdocumento" => "sco"
    "cita" => "An Pediatr (Barc). 2000;52:271-4"
    "abierto" => array:3 [
      "ES" => false
      "ES2" => false
      "LATM" => false
    ]
    "gratuito" => false
    "lecturas" => array:2 [
      "total" => 4141
      "formatos" => array:3 [
        "EPUB" => 63
        "HTML" => 3569
        "PDF" => 509
      ]
    ]
    "es" => array:10 [
      "idiomaDefecto" => true
      "titulo" => "Seudoquiste pulmonar traumático"
      "tienePdf" => "es"
      "tieneTextoCompleto" => 0
      "tieneResumen" => array:2 [
        0 => "es"
        1 => "en"
      ]
      "paginas" => array:1 [
        0 => array:2 [
          "paginaInicial" => "271"
          "paginaFinal" => "274"
        ]
      ]
      "titulosAlternativos" => array:1 [
        "en" => array:1 [
          "titulo" => "Traumatic Pulmonary Pseudocyst"
        ]
      ]
      "contieneResumen" => array:2 [
        "es" => true
        "en" => true
      ]
      "contienePdf" => array:1 [
        "es" => true
      ]
      "autores" => array:1 [
        0 => array:2 [
          "autoresLista" => "A. Díaz Conradi, M. Carreras Lavila, A. García-Henares, R. García-Pagán, A. Moral García, M. Mateu Navarro, L. Tobeña Boada"
          "autores" => array:7 [
            0 => array:2 [
              "nombre" => "A."
              "apellidos" => "Díaz Conradi"
            ]
            1 => array:2 [
              "nombre" => "M."
              "apellidos" => "Carreras Lavila"
            ]
            2 => array:2 [
              "nombre" => "A."
              "apellidos" => "García-Henares"
            ]
            3 => array:2 [
              "nombre" => "R."
              "apellidos" => "García-Pagán"
            ]
            4 => array:2 [
              "nombre" => "A."
              "apellidos" => "Moral García"
            ]
            5 => array:2 [
              "nombre" => "M."
              "apellidos" => "Mateu Navarro"
            ]
            6 => array:2 [
              "nombre" => "L."
              "apellidos" => "Tobeña Boada"
            ]
          ]
        ]
      ]
    ]
    "idiomaDefecto" => "es"
    "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403300773371?idApp=UINPBA00005H"
    "url" => "/16954033/0000005200000003/v1_201307051451/S1695403300773371/v1_201307051451/es/main.assets"
  ]
  "itemAnterior" => array:18 [
    "pii" => "S1695403300773358"
    "issn" => "16954033"
    "doi" => "10.1016/S1695-4033(00)77335-8"
    "estado" => "S300"
    "fechaPublicacion" => "2000-03-01"
    "aid" => "77335"
    "copyright" => "Asociación Española de Pediatría"
    "documento" => "article"
    "crossmark" => 0
    "subdocumento" => "sco"
    "cita" => "An Pediatr (Barc). 2000;52:263-6"
    "abierto" => array:3 [
      "ES" => false
      "ES2" => false
      "LATM" => false
    ]
    "gratuito" => false
    "lecturas" => array:2 [
      "total" => 2332
      "formatos" => array:3 [
        "EPUB" => 69
        "HTML" => 1447
        "PDF" => 816
      ]
    ]
    "es" => array:10 [
      "idiomaDefecto" => true
      "titulo" => "Síndrome del shock tóxico en niños. Presentación de 4 casos"
      "tienePdf" => "es"
      "tieneTextoCompleto" => 0
      "tieneResumen" => array:2 [
        0 => "es"
        1 => "en"
      ]
      "paginas" => array:1 [
        0 => array:2 [
          "paginaInicial" => "263"
          "paginaFinal" => "266"
        ]
      ]
      "titulosAlternativos" => array:1 [
        "en" => array:1 [
          "titulo" => "Toxic Shock Syndrome In Children. Report Of Four Cases"
        ]
      ]
      "contieneResumen" => array:2 [
        "es" => true
        "en" => true
      ]
      "contienePdf" => array:1 [
        "es" => true
      ]
      "autores" => array:1 [
        0 => array:2 [
          "autoresLista" => "A. de Vicente Aymat, A. Martínez de Azagra, S. Mencía Bartolomé, A. Serrano González, J. Casado Flores"
          "autores" => array:5 [
            0 => array:2 [
              "nombre" => "A."
              "apellidos" => "de Vicente Aymat"
            ]
            1 => array:2 [
              "nombre" => "A."
              "apellidos" => "Martínez de Azagra"
            ]
            2 => array:2 [
              "nombre" => "S."
              "apellidos" => "Mencía Bartolomé"
            ]
            3 => array:2 [
              "nombre" => "A."
              "apellidos" => "Serrano González"
            ]
            4 => array:2 [
              "nombre" => "J."
              "apellidos" => "Casado Flores"
            ]
          ]
        ]
      ]
    ]
    "idiomaDefecto" => "es"
    "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403300773358?idApp=UINPBA00005H"
    "url" => "/16954033/0000005200000003/v1_201307051451/S1695403300773358/v1_201307051451/es/main.assets"
  ]
  "asociados" => array:1 [
    0 => array:18 [
      "pii" => "S1695403300774029"
      "issn" => "16954033"
      "doi" => "10.1016/S1695-4033(00)77402-9"
      "estado" => "S300"
      "fechaPublicacion" => "2000-06-01"
      "aid" => "77402"
      "copyright" => "Asociación Española de Pediatría"
      "documento" => "simple-article"
      "crossmark" => 0
      "subdocumento" => "err"
      "cita" => "An Pediatr (Barc). 2000;52:568"
      "abierto" => array:3 [
        "ES" => false
        "ES2" => false
        "LATM" => false
      ]
      "gratuito" => false
      "lecturas" => array:2 [
        "total" => 896
        "formatos" => array:3 [
          "EPUB" => 60
          "HTML" => 506
          "PDF" => 330
        ]
      ]
      "es" => array:6 [
        "idiomaDefecto" => true
        "titulo" => "Fe de errores"
        "tienePdf" => "es"
        "tieneTextoCompleto" => 0
        "paginas" => array:1 [
          0 => array:1 [
            "paginaInicial" => "568"
          ]
        ]
        "contienePdf" => array:1 [
          "es" => true
        ]
      ]
      "idiomaDefecto" => "es"
      "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403300774029?idApp=UINPBA00005H"
      "url" => "/16954033/0000005200000006/v1_201307051505/S1695403300774029/v1_201307051505/es/main.assets"
    ]
  ]
  "es" => array:14 [
    "idiomaDefecto" => true
    "titulo" => "Hiperferritinemia aislada en un lactante sano: síndrome hereditario de hiperferritinemia y cataratas"
    "tieneTextoCompleto" => 0
    "paginas" => array:1 [
      0 => array:2 [
        "paginaInicial" => "267"
        "paginaFinal" => "270"
      ]
    ]
    "autores" => array:1 [
      0 => array:4 [
        "autoresLista" => "A. Cervera Bravo, M. Sebastián Planas, A. Alarabe Alarabe, A. Díez Sáenz, M.J. Avilés Egea, A. Balas Pérez"
        "autores" => array:6 [
          0 => array:3 [
            "nombre" => "A."
            "apellidos" => "Cervera Bravo"
            "referencia" => array:2 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
              1 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">&#42;</span>"
                "identificador" => "cor0005"
              ]
            ]
          ]
          1 => array:3 [
            "nombre" => "M&#46;"
            "apellidos" => "Sebasti&#225;n Planas"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
            ]
          ]
          2 => array:3 [
            "nombre" => "A&#46;"
            "apellidos" => "Alarabe Alarabe"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
            ]
          ]
          3 => array:3 [
            "nombre" => "A&#46;"
            "apellidos" => "D&#237;ez S&#225;enz"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
            ]
          ]
          4 => array:3 [
            "nombre" => "M&#46;J&#46;"
            "apellidos" => "Avil&#233;s Egea"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">b</span>"
                "identificador" => "aff0010"
              ]
            ]
          ]
          5 => array:3 [
            "nombre" => "A&#46;"
            "apellidos" => "Balas P&#233;rez"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">b</span>"
                "identificador" => "aff0010"
              ]
            ]
          ]
        ]
        "afiliaciones" => array:2 [
          0 => array:3 [
            "entidad" => "Servicio de Pediatr&#237;a&#46; Hospital de M&#243;stoles&#46; Madrid"
            "etiqueta" => "<span class="elsevierStyleSup">a</span>"
            "identificador" => "aff0005"
          ]
          1 => array:3 [
            "entidad" => "Laboratorio de Histocompatibilidad y Biolog&#237;a Molecular&#46; Centro Regional de Transfusi&#243;n&#46; Madrid"
            "etiqueta" => "<span class="elsevierStyleSup">b</span>"
            "identificador" => "aff0010"
          ]
        ]
        "correspondencia" => array:1 [
          0 => array:3 [
            "identificador" => "cor0005"
            "etiqueta" => "&#42;"
            "correspondencia" => "Servicio de Pediatr&#237;a&#46; Hospital de M&#243;stoles&#46; R&#237;o J&#250;car S&#47;N&#46; 28935 M&#243;stoles&#44; Madrid"
          ]
        ]
      ]
    ]
    "titulosAlternativos" => array:1 [
      "en" => array:1 [
        "titulo" => "Isolated hyperferritinemia In a healthy male infant&#58; hereditary Hyperferritinemia-cataract syndrome"
      ]
    ]
    "pdfFichero" => "main.pdf"
    "tienePdf" => true
    "fechaRecibido" => "1999-04-30"
    "fechaAceptado" => "1999-05-31"
    "PalabrasClave" => array:1 [
      "es" => array:1 [
        0 => array:4 [
          "clase" => "keyword"
          "titulo" => "Palabras clave"
          "identificador" => "xpalclavsec186251"
          "palabras" => array:3 [
            0 => "Hiperferritinemia"
            1 => "Cataratas cong&#233;nitas"
            2 => "Metabolismo del hierro"
          ]
        ]
      ]
    ]
    "tieneResumen" => true
    "resumen" => array:2 [
      "es" => array:1 [
        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Se describe el caso de un lactante var&#243;n con hallazgo casual de hiperferritinemia a los 3 meses&#44; a trav&#233;s del cual se lleg&#243; al diagn&#243;stico en varios familiares de 3 generaciones de s&#237;ndrome hereditario de hiperferritinemia y cataratas&#44; con una nueva mutaci&#243;n puntual en el IRE del gende la L-ferritina&#46; Se comenta el diagn&#243;stico diferencial de las hiperferritinemias&#44; haciendo hincapi&#233; en el conocimiento de esta entidad para evitar exploraciones innecesarias&#46;</p>"
      ]
      "en" => array:1 [
        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">The case of a male infant who was found to have hyperferritinemia was made at the age of 3 months is described&#46; The patient and several members of his family from three generations were diagnosed with hereditary hyperferritinemia-cataract syndrome with a new point mutation in the iron-responsive element of the L-ferritin gene&#46; Differential diagnosis of hyperferritinemia is discussed with emphasis on the need for the knowledge of this entity to avoid unnecessary investigations&#46;</p>"
      ]
    ]
    "bibliografia" => array:2 [
      "titulo" => "Bibliograf&#237;a"
      "seccion" => array:1 [
        0 => array:2 [
          "identificador" => "bibs0005"
          "bibliografiaReferencia" => array:17 [
            0 => array:3 [
              "identificador" => "bib0005"
              "etiqueta" => "1&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "A linkage between hereditary hyperferritinemia not related to iron overload and autosomal dominant congenital cataract"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "D&#46; Girelli"
                            1 => "O&#46; Olivieri"
                            2 => "L&#46; De Franceschi"
                            3 => "R&#46; Corrocher"
                            4 => "G&#46; Berga-maschi"
                            5 => "M&#46; Cazzola"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Br J Haematol"
                        "fecha" => "1995"
                        "volumen" => "90"
                        "paginaInicial" => "931"
                        "paginaFinal" => "934"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/7669675"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            1 => array:3 [
              "identificador" => "bib0010"
              "etiqueta" => "2&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Bilateral cataract and high serum ferritin&#58; a new dominant genetic disorder&#945;"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "D&#46; Bonneau"
                            1 => "I&#46; Winter-Fuseau"
                            2 => "M&#46;N&#46; Loiseau"
                            3 => "P&#46; Amati"
                            4 => "M&#46; Berthier"
                            5 => "D&#46; Oriot"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "J Med Genet"
                        "fecha" => "1995"
                        "volumen" => "32"
                        "paginaInicial" => "778"
                        "paginaFinal" => "779"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/8558554"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            2 => array:3 [
              "identificador" => "bib0015"
              "etiqueta" => "3&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome&#58; a mutation in the iron-responsive element of ferritin L-subunit gene &#40;the&#8220;Verona mutation&#8221;&#41;"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "D&#46; Girelli"
                            1 => "R&#46; Corrocher"
                            2 => "L&#46; Bisceglia"
                            3 => "O&#46; Olivieri"
                            4 => "L&#46; De Franceschi"
                            5 => "L&#46; Zelante"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1995"
                        "volumen" => "86"
                        "paginaInicial" => "4050"
                        "paginaFinal" => "4053"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/7492760"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            3 => array:3 [
              "identificador" => "bib0020"
              "etiqueta" => "4&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Mutation in the iron responsive element of L ferritin mRNA in a family with do-minant hyperferritinemia and cataract"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "C&#46; Beaumont"
                            1 => "P&#46; Lenevue"
                            2 => "I&#46; Devaux"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1038/ng1295-444"
                      "Revista" => array:6 [
                        "tituloSerie" => "Nat Genet"
                        "fecha" => "1995"
                        "volumen" => "11"
                        "paginaInicial" => "444"
                        "paginaFinal" => "446"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/7493028"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            4 => array:3 [
              "identificador" => "bib0025"
              "etiqueta" => "5&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:5 [
                            0 => "P&#46; Aguilar-Mart&#237;nez"
                            1 => "C&#46; Biron"
                            2 => "C&#46; Masmejean"
                            3 => "P&#46; Jeanjean"
                            4 => "J&#46;F&#46; Schved"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1996"
                        "volumen" => "88"
                        "paginaInicial" => "1895"
                        "paginaFinal" => "1896"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/8781450"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            5 => array:3 [
              "identificador" => "bib0030"
              "etiqueta" => "6&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hereditary hyperferritinemia-cataract syndrome&#58; relation between phenotypes and specific mutations in the iron- responsive element of ferritin light-chain mRNA"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "M&#46; Cazzola"
                            1 => "G&#46; Bergamaschi"
                            2 => "L&#46; Tonon"
                            3 => "E&#46; Arbustini"
                            4 => "M&#46; Grasso"
                            5 => "E&#46; Vercesi"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1997"
                        "volumen" => "90"
                        "paginaInicial" => "814"
                        "paginaFinal" => "821"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9226182"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            6 => array:3 [
              "identificador" => "bib0035"
              "etiqueta" => "7&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron-responsive element of ferritin L-subunit gene"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "D&#46; Girelli"
                            1 => "R&#46; Corrocher"
                            2 => "L&#46; Bisceglia"
                            3 => "O&#46; Olivieri"
                            4 => "L&#46; Zelante"
                            5 => "G&#46; Pa-nozzo"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1997"
                        "volumen" => "90"
                        "paginaInicial" => "2084"
                        "paginaFinal" => "2088"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9292547"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            7 => array:3 [
              "identificador" => "bib0040"
              "etiqueta" => "8&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "A point mutation in the bulge of the iron-responsive element of the L-ferritin gene in two families with the hereditary hyperferri-tinemia-cataract syndrome"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:5 [
                            0 => "M&#46;E&#46; Martin"
                            1 => "S&#46; Fargion"
                            2 => "P&#46; Brissot"
                            3 => "B&#46; Pellat"
                            4 => "C&#46; Beaumont"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1998"
                        "volumen" => "91"
                        "paginaInicial" => "319"
                        "paginaFinal" => "323"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9414300"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            8 => array:3 [
              "identificador" => "bib0045"
              "etiqueta" => "9&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hereditary hyperferriti-nemia-cataract syndrome&#58; two novel mutations in the L-ferritin iron-responsive element"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "A&#46;D&#46; Munford"
                            1 => "T&#46; Vulliamy"
                            2 => "J&#46; Lindsay"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1998"
                        "volumen" => "91"
                        "paginaInicial" => "367"
                        "paginaFinal" => "368"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9414313"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            9 => array:3 [
              "identificador" => "bib0050"
              "etiqueta" => "10&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Description of a new mutation in the L-ferritin iron-responsi-ve element associated with hereditary hyperferritinemia-cataract syndrome in a spanish family"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:5 [
                            0 => "A&#46; Balas"
                            1 => "M&#46;J&#46; Avil&#233;s"
                            2 => "F&#46; Garc&#237;a-S&#225;nchez"
                            3 => "J&#46;L&#46; Vicario"
                            4 => "A&#46; Cervera"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1999"
                        "volumen" => "93"
                        "paginaInicial" => "4020"
                        "paginaFinal" => "4021"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/10383191"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            10 => array:3 [
              "identificador" => "bib0055"
              "etiqueta" => "11&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Function and regulation of transferrin and ferritin"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "P&#46; Ponka"
                            1 => "C&#46; Beaumont"
                            2 => "D&#46;R&#46; Richardson"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Semin Hematol"
                        "fecha" => "1998"
                        "volumen" => "35"
                        "paginaInicial" => "35"
                        "paginaFinal" => "54"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9460808"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            11 => array:3 [
              "identificador" => "bib0060"
              "etiqueta" => "12&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hemochromatosis and iron metabolism"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "T&#46;A&#46; Rouault"
                            1 => "M&#46;A&#46; Hediger"
                            2 => "N&#46;C&#46; Andrews"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:5 [
                        "tituloSerie" => "Gastroenterology"
                        "fecha" => "1999"
                        "volumen" => "116"
                        "paginaInicial" => "194"
                        "paginaFinal" => "195"
                      ]
                    ]
                  ]
                ]
              ]
            ]
            12 => array:3 [
              "identificador" => "bib0065"
              "etiqueta" => "13&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Thyroid hormo-ne modulates the interaction between iron regulatory pro-teins and the ferritin mRNA iron responsive element"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:4 [
                            0 => "P&#46;J&#46; Leedman"
                            1 => "A&#46;R&#46; Stein"
                            2 => "W&#46;W&#46; Chin"
                            3 => "J&#46;T&#46; Rogers"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:5 [
                        "tituloSerie" => "J Biol Chem"
                        "fecha" => "1996"
                        "volumen" => "12"
                        "paginaInicial" => "12017"
                        "paginaFinal" => "12023"
                      ]
                    ]
                  ]
                ]
              ]
            ]
            13 => array:3 [
              "identificador" => "bib0070"
              "etiqueta" => "14&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hipertiroidismo&#44; otra causa de hiperferritinemia"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "M&#46; Rozman"
                            1 => "J&#46;L&#46; Vives Corrons"
                            2 => "C&#46; Rozman"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:4 [
                        "tituloSerie" => "Med Clin &#40;Barc&#41;"
                        "fecha" => "1992"
                        "volumen" => "99"
                        "paginaInicial" => "273"
                      ]
                    ]
                  ]
                ]
              ]
            ]
            14 => array:3 [
              "identificador" => "bib0075"
              "etiqueta" => "15&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Secondary iron overload disorders"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:1 [
                            0 => "S&#46;S&#46; Bottomley"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:5 [
                        "tituloSerie" => "Semin He-matol"
                        "fecha" => "1998"
                        "volumen" => "35"
                        "paginaInicial" => "77"
                        "paginaFinal" => "86"
                      ]
                    ]
                  ]
                ]
              ]
            ]
            15 => array:3 [
              "identificador" => "bib0080"
              "etiqueta" => "16&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Screening for hemochromatosis"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:2 [
                            0 => "C&#46;Q&#46; Edwards"
                            1 => "J&#46;P&#46; Kushner"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1056/NEJM199306033282208"
                      "Revista" => array:6 [
                        "tituloSerie" => "N Engl J Med"
                        "fecha" => "1993"
                        "volumen" => "328"
                        "paginaInicial" => "1616"
                        "paginaFinal" => "1620"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/8110209"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            16 => array:3 [
              "identificador" => "bib0085"
              "etiqueta" => "17&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Analysis of ferritins in lymphoblastoid cell lines and the lens of subjects with hereditary hyperferritinemia-cataract syndrome"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "S&#46; Levi"
                            1 => "D&#46; Girelli"
                            2 => "F&#46; Perrone"
                            3 => "M&#46; Pasti"
                            4 => "C&#46; Beaumont"
                            5 => "R&#46; Corrocher"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1998"
                        "volumen" => "91"
                        "paginaInicial" => "4180"
                        "paginaFinal" => "4187"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9596665"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
          ]
        ]
      ]
    ]
  ]
  "idiomaDefecto" => "es"
  "url" => "/16954033/0000005200000003/v1_201307051451/S169540330077336X/v1_201307051451/es/main.assets"
  "Apartado" => array:4 [
    "identificador" => "14441"
    "tipo" => "SECCION"
    "es" => array:2 [
      "titulo" => "Notas cl&#237;nicas"
      "idiomaDefecto" => true
    ]
    "idiomaDefecto" => "es"
  ]
  "PDF" => "https://static.elsevier.es/multimedia/16954033/0000005200000003/v1_201307051451/S169540330077336X/v1_201307051451/es/main.pdf?idApp=UINPBA00005H&text.app=https://analesdepediatria.org/"
  "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S169540330077336X?idApp=UINPBA00005H"
]
Compartir
Información de la revista

Estadísticas

Siga este enlace para acceder al texto completo del artículo

Hiperferritinemia aislada en un lactante sano: síndrome hereditario de hiperferritinemia y cataratas
Isolated hyperferritinemia In a healthy male infant: hereditary Hyperferritinemia-cataract syndrome
A. Cervera Bravoa,*, M. Sebastián Planasa, A. Alarabe Alarabea, A. Díez Sáenza, M.J. Avilés Egeab, A. Balas Pérezb
a Servicio de Pediatría. Hospital de Móstoles. Madrid
b Laboratorio de Histocompatibilidad y Biología Molecular. Centro Regional de Transfusión. Madrid
Leído
11109
Veces
se ha leído el artículo
3482
Total PDF
7627
Total HTML
Compartir estadísticas
 array:24 [
  "pii" => "S169540330077336X"
  "issn" => "16954033"
  "doi" => "10.1016/S1695-4033(00)77336-X"
  "estado" => "S300"
  "fechaPublicacion" => "2000-03-01"
  "aid" => "77336"
  "copyright" => "Asociaci&#243;n Espa&#241;ola de Pediatr&#237;a"
  "copyrightAnyo" => "2000"
  "documento" => "article"
  "crossmark" => 0
  "subdocumento" => "sco"
  "cita" => "An Pediatr &#40;Barc&#41;. 2000;52:267-70"
  "abierto" => array:3 [
    "ES" => false
    "ES2" => false
    "LATM" => false
  ]
  "gratuito" => false
  "lecturas" => array:2 [
    "total" => 5847
    "formatos" => array:3 [
      "EPUB" => 88
      "HTML" => 4745
      "PDF" => 1014
    ]
  ]
  "itemSiguiente" => array:18 [
    "pii" => "S1695403300773371"
    "issn" => "16954033"
    "doi" => "10.1016/S1695-4033(00)77337-1"
    "estado" => "S300"
    "fechaPublicacion" => "2000-03-01"
    "aid" => "77337"
    "copyright" => "Asociaci&#243;n Espa&#241;ola de Pediatr&#237;a"
    "documento" => "article"
    "crossmark" => 0
    "subdocumento" => "sco"
    "cita" => "An Pediatr &#40;Barc&#41;. 2000;52:271-4"
    "abierto" => array:3 [
      "ES" => false
      "ES2" => false
      "LATM" => false
    ]
    "gratuito" => false
    "lecturas" => array:2 [
      "total" => 4141
      "formatos" => array:3 [
        "EPUB" => 63
        "HTML" => 3569
        "PDF" => 509
      ]
    ]
    "es" => array:10 [
      "idiomaDefecto" => true
      "titulo" => "Seudoquiste pulmonar traum&#225;tico"
      "tienePdf" => "es"
      "tieneTextoCompleto" => 0
      "tieneResumen" => array:2 [
        0 => "es"
        1 => "en"
      ]
      "paginas" => array:1 [
        0 => array:2 [
          "paginaInicial" => "271"
          "paginaFinal" => "274"
        ]
      ]
      "titulosAlternativos" => array:1 [
        "en" => array:1 [
          "titulo" => "Traumatic Pulmonary Pseudocyst"
        ]
      ]
      "contieneResumen" => array:2 [
        "es" => true
        "en" => true
      ]
      "contienePdf" => array:1 [
        "es" => true
      ]
      "autores" => array:1 [
        0 => array:2 [
          "autoresLista" => "A&#46; D&#237;az Conradi, M&#46; Carreras Lavila, A&#46; Garc&#237;a-Henares, R&#46; Garc&#237;a-Pag&#225;n, A&#46; Moral Garc&#237;a, M&#46; Mateu Navarro, L&#46; Tobe&#241;a Boada"
          "autores" => array:7 [
            0 => array:2 [
              "nombre" => "A&#46;"
              "apellidos" => "D&#237;az Conradi"
            ]
            1 => array:2 [
              "nombre" => "M&#46;"
              "apellidos" => "Carreras Lavila"
            ]
            2 => array:2 [
              "nombre" => "A&#46;"
              "apellidos" => "Garc&#237;a-Henares"
            ]
            3 => array:2 [
              "nombre" => "R&#46;"
              "apellidos" => "Garc&#237;a-Pag&#225;n"
            ]
            4 => array:2 [
              "nombre" => "A&#46;"
              "apellidos" => "Moral Garc&#237;a"
            ]
            5 => array:2 [
              "nombre" => "M&#46;"
              "apellidos" => "Mateu Navarro"
            ]
            6 => array:2 [
              "nombre" => "L&#46;"
              "apellidos" => "Tobe&#241;a Boada"
            ]
          ]
        ]
      ]
    ]
    "idiomaDefecto" => "es"
    "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403300773371?idApp=UINPBA00005H"
    "url" => "/16954033/0000005200000003/v1_201307051451/S1695403300773371/v1_201307051451/es/main.assets"
  ]
  "itemAnterior" => array:18 [
    "pii" => "S1695403300773358"
    "issn" => "16954033"
    "doi" => "10.1016/S1695-4033(00)77335-8"
    "estado" => "S300"
    "fechaPublicacion" => "2000-03-01"
    "aid" => "77335"
    "copyright" => "Asociaci&#243;n Espa&#241;ola de Pediatr&#237;a"
    "documento" => "article"
    "crossmark" => 0
    "subdocumento" => "sco"
    "cita" => "An Pediatr &#40;Barc&#41;. 2000;52:263-6"
    "abierto" => array:3 [
      "ES" => false
      "ES2" => false
      "LATM" => false
    ]
    "gratuito" => false
    "lecturas" => array:2 [
      "total" => 2332
      "formatos" => array:3 [
        "EPUB" => 69
        "HTML" => 1447
        "PDF" => 816
      ]
    ]
    "es" => array:10 [
      "idiomaDefecto" => true
      "titulo" => "S&#237;ndrome del shock t&#243;xico en ni&#241;os&#46; Presentaci&#243;n de 4 casos"
      "tienePdf" => "es"
      "tieneTextoCompleto" => 0
      "tieneResumen" => array:2 [
        0 => "es"
        1 => "en"
      ]
      "paginas" => array:1 [
        0 => array:2 [
          "paginaInicial" => "263"
          "paginaFinal" => "266"
        ]
      ]
      "titulosAlternativos" => array:1 [
        "en" => array:1 [
          "titulo" => "Toxic Shock Syndrome In Children&#46; Report Of Four Cases"
        ]
      ]
      "contieneResumen" => array:2 [
        "es" => true
        "en" => true
      ]
      "contienePdf" => array:1 [
        "es" => true
      ]
      "autores" => array:1 [
        0 => array:2 [
          "autoresLista" => "A&#46; de Vicente Aymat, A&#46; Mart&#237;nez de Azagra, S&#46; Menc&#237;a Bartolom&#233;, A&#46; Serrano Gonz&#225;lez, J&#46; Casado Flores"
          "autores" => array:5 [
            0 => array:2 [
              "nombre" => "A&#46;"
              "apellidos" => "de Vicente Aymat"
            ]
            1 => array:2 [
              "nombre" => "A&#46;"
              "apellidos" => "Mart&#237;nez de Azagra"
            ]
            2 => array:2 [
              "nombre" => "S&#46;"
              "apellidos" => "Menc&#237;a Bartolom&#233;"
            ]
            3 => array:2 [
              "nombre" => "A&#46;"
              "apellidos" => "Serrano Gonz&#225;lez"
            ]
            4 => array:2 [
              "nombre" => "J&#46;"
              "apellidos" => "Casado Flores"
            ]
          ]
        ]
      ]
    ]
    "idiomaDefecto" => "es"
    "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403300773358?idApp=UINPBA00005H"
    "url" => "/16954033/0000005200000003/v1_201307051451/S1695403300773358/v1_201307051451/es/main.assets"
  ]
  "asociados" => array:1 [
    0 => array:18 [
      "pii" => "S1695403300774029"
      "issn" => "16954033"
      "doi" => "10.1016/S1695-4033(00)77402-9"
      "estado" => "S300"
      "fechaPublicacion" => "2000-06-01"
      "aid" => "77402"
      "copyright" => "Asociaci&#243;n Espa&#241;ola de Pediatr&#237;a"
      "documento" => "simple-article"
      "crossmark" => 0
      "subdocumento" => "err"
      "cita" => "An Pediatr &#40;Barc&#41;. 2000;52:568"
      "abierto" => array:3 [
        "ES" => false
        "ES2" => false
        "LATM" => false
      ]
      "gratuito" => false
      "lecturas" => array:2 [
        "total" => 896
        "formatos" => array:3 [
          "EPUB" => 60
          "HTML" => 506
          "PDF" => 330
        ]
      ]
      "es" => array:6 [
        "idiomaDefecto" => true
        "titulo" => "Fe de errores"
        "tienePdf" => "es"
        "tieneTextoCompleto" => 0
        "paginas" => array:1 [
          0 => array:1 [
            "paginaInicial" => "568"
          ]
        ]
        "contienePdf" => array:1 [
          "es" => true
        ]
      ]
      "idiomaDefecto" => "es"
      "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403300774029?idApp=UINPBA00005H"
      "url" => "/16954033/0000005200000006/v1_201307051505/S1695403300774029/v1_201307051505/es/main.assets"
    ]
  ]
  "es" => array:14 [
    "idiomaDefecto" => true
    "titulo" => "Hiperferritinemia aislada en un lactante sano&#58; s&#237;ndrome hereditario de hiperferritinemia y cataratas"
    "tieneTextoCompleto" => 0
    "paginas" => array:1 [
      0 => array:2 [
        "paginaInicial" => "267"
        "paginaFinal" => "270"
      ]
    ]
    "autores" => array:1 [
      0 => array:4 [
        "autoresLista" => "A&#46; Cervera Bravo, M&#46; Sebasti&#225;n Planas, A&#46; Alarabe Alarabe, A&#46; D&#237;ez S&#225;enz, M&#46;J&#46; Avil&#233;s Egea, A&#46; Balas P&#233;rez"
        "autores" => array:6 [
          0 => array:3 [
            "nombre" => "A&#46;"
            "apellidos" => "Cervera Bravo"
            "referencia" => array:2 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
              1 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">&#42;</span>"
                "identificador" => "cor0005"
              ]
            ]
          ]
          1 => array:3 [
            "nombre" => "M&#46;"
            "apellidos" => "Sebasti&#225;n Planas"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
            ]
          ]
          2 => array:3 [
            "nombre" => "A&#46;"
            "apellidos" => "Alarabe Alarabe"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
            ]
          ]
          3 => array:3 [
            "nombre" => "A&#46;"
            "apellidos" => "D&#237;ez S&#225;enz"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
            ]
          ]
          4 => array:3 [
            "nombre" => "M&#46;J&#46;"
            "apellidos" => "Avil&#233;s Egea"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">b</span>"
                "identificador" => "aff0010"
              ]
            ]
          ]
          5 => array:3 [
            "nombre" => "A&#46;"
            "apellidos" => "Balas P&#233;rez"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">b</span>"
                "identificador" => "aff0010"
              ]
            ]
          ]
        ]
        "afiliaciones" => array:2 [
          0 => array:3 [
            "entidad" => "Servicio de Pediatr&#237;a&#46; Hospital de M&#243;stoles&#46; Madrid"
            "etiqueta" => "<span class="elsevierStyleSup">a</span>"
            "identificador" => "aff0005"
          ]
          1 => array:3 [
            "entidad" => "Laboratorio de Histocompatibilidad y Biolog&#237;a Molecular&#46; Centro Regional de Transfusi&#243;n&#46; Madrid"
            "etiqueta" => "<span class="elsevierStyleSup">b</span>"
            "identificador" => "aff0010"
          ]
        ]
        "correspondencia" => array:1 [
          0 => array:3 [
            "identificador" => "cor0005"
            "etiqueta" => "&#42;"
            "correspondencia" => "Servicio de Pediatr&#237;a&#46; Hospital de M&#243;stoles&#46; R&#237;o J&#250;car S&#47;N&#46; 28935 M&#243;stoles&#44; Madrid"
          ]
        ]
      ]
    ]
    "titulosAlternativos" => array:1 [
      "en" => array:1 [
        "titulo" => "Isolated hyperferritinemia In a healthy male infant&#58; hereditary Hyperferritinemia-cataract syndrome"
      ]
    ]
    "pdfFichero" => "main.pdf"
    "tienePdf" => true
    "fechaRecibido" => "1999-04-30"
    "fechaAceptado" => "1999-05-31"
    "PalabrasClave" => array:1 [
      "es" => array:1 [
        0 => array:4 [
          "clase" => "keyword"
          "titulo" => "Palabras clave"
          "identificador" => "xpalclavsec186251"
          "palabras" => array:3 [
            0 => "Hiperferritinemia"
            1 => "Cataratas cong&#233;nitas"
            2 => "Metabolismo del hierro"
          ]
        ]
      ]
    ]
    "tieneResumen" => true
    "resumen" => array:2 [
      "es" => array:1 [
        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Se describe el caso de un lactante var&#243;n con hallazgo casual de hiperferritinemia a los 3 meses&#44; a trav&#233;s del cual se lleg&#243; al diagn&#243;stico en varios familiares de 3 generaciones de s&#237;ndrome hereditario de hiperferritinemia y cataratas&#44; con una nueva mutaci&#243;n puntual en el IRE del gende la L-ferritina&#46; Se comenta el diagn&#243;stico diferencial de las hiperferritinemias&#44; haciendo hincapi&#233; en el conocimiento de esta entidad para evitar exploraciones innecesarias&#46;</p>"
      ]
      "en" => array:1 [
        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">The case of a male infant who was found to have hyperferritinemia was made at the age of 3 months is described&#46; The patient and several members of his family from three generations were diagnosed with hereditary hyperferritinemia-cataract syndrome with a new point mutation in the iron-responsive element of the L-ferritin gene&#46; Differential diagnosis of hyperferritinemia is discussed with emphasis on the need for the knowledge of this entity to avoid unnecessary investigations&#46;</p>"
      ]
    ]
    "bibliografia" => array:2 [
      "titulo" => "Bibliograf&#237;a"
      "seccion" => array:1 [
        0 => array:2 [
          "identificador" => "bibs0005"
          "bibliografiaReferencia" => array:17 [
            0 => array:3 [
              "identificador" => "bib0005"
              "etiqueta" => "1&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "A linkage between hereditary hyperferritinemia not related to iron overload and autosomal dominant congenital cataract"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "D&#46; Girelli"
                            1 => "O&#46; Olivieri"
                            2 => "L&#46; De Franceschi"
                            3 => "R&#46; Corrocher"
                            4 => "G&#46; Berga-maschi"
                            5 => "M&#46; Cazzola"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Br J Haematol"
                        "fecha" => "1995"
                        "volumen" => "90"
                        "paginaInicial" => "931"
                        "paginaFinal" => "934"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/7669675"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            1 => array:3 [
              "identificador" => "bib0010"
              "etiqueta" => "2&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Bilateral cataract and high serum ferritin&#58; a new dominant genetic disorder&#945;"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "D&#46; Bonneau"
                            1 => "I&#46; Winter-Fuseau"
                            2 => "M&#46;N&#46; Loiseau"
                            3 => "P&#46; Amati"
                            4 => "M&#46; Berthier"
                            5 => "D&#46; Oriot"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "J Med Genet"
                        "fecha" => "1995"
                        "volumen" => "32"
                        "paginaInicial" => "778"
                        "paginaFinal" => "779"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/8558554"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            2 => array:3 [
              "identificador" => "bib0015"
              "etiqueta" => "3&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome&#58; a mutation in the iron-responsive element of ferritin L-subunit gene &#40;the&#8220;Verona mutation&#8221;&#41;"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "D&#46; Girelli"
                            1 => "R&#46; Corrocher"
                            2 => "L&#46; Bisceglia"
                            3 => "O&#46; Olivieri"
                            4 => "L&#46; De Franceschi"
                            5 => "L&#46; Zelante"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1995"
                        "volumen" => "86"
                        "paginaInicial" => "4050"
                        "paginaFinal" => "4053"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/7492760"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            3 => array:3 [
              "identificador" => "bib0020"
              "etiqueta" => "4&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Mutation in the iron responsive element of L ferritin mRNA in a family with do-minant hyperferritinemia and cataract"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "C&#46; Beaumont"
                            1 => "P&#46; Lenevue"
                            2 => "I&#46; Devaux"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1038/ng1295-444"
                      "Revista" => array:6 [
                        "tituloSerie" => "Nat Genet"
                        "fecha" => "1995"
                        "volumen" => "11"
                        "paginaInicial" => "444"
                        "paginaFinal" => "446"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/7493028"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            4 => array:3 [
              "identificador" => "bib0025"
              "etiqueta" => "5&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:5 [
                            0 => "P&#46; Aguilar-Mart&#237;nez"
                            1 => "C&#46; Biron"
                            2 => "C&#46; Masmejean"
                            3 => "P&#46; Jeanjean"
                            4 => "J&#46;F&#46; Schved"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1996"
                        "volumen" => "88"
                        "paginaInicial" => "1895"
                        "paginaFinal" => "1896"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/8781450"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            5 => array:3 [
              "identificador" => "bib0030"
              "etiqueta" => "6&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hereditary hyperferritinemia-cataract syndrome&#58; relation between phenotypes and specific mutations in the iron- responsive element of ferritin light-chain mRNA"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "M&#46; Cazzola"
                            1 => "G&#46; Bergamaschi"
                            2 => "L&#46; Tonon"
                            3 => "E&#46; Arbustini"
                            4 => "M&#46; Grasso"
                            5 => "E&#46; Vercesi"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1997"
                        "volumen" => "90"
                        "paginaInicial" => "814"
                        "paginaFinal" => "821"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9226182"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            6 => array:3 [
              "identificador" => "bib0035"
              "etiqueta" => "7&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron-responsive element of ferritin L-subunit gene"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "D&#46; Girelli"
                            1 => "R&#46; Corrocher"
                            2 => "L&#46; Bisceglia"
                            3 => "O&#46; Olivieri"
                            4 => "L&#46; Zelante"
                            5 => "G&#46; Pa-nozzo"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1997"
                        "volumen" => "90"
                        "paginaInicial" => "2084"
                        "paginaFinal" => "2088"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9292547"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            7 => array:3 [
              "identificador" => "bib0040"
              "etiqueta" => "8&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "A point mutation in the bulge of the iron-responsive element of the L-ferritin gene in two families with the hereditary hyperferri-tinemia-cataract syndrome"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:5 [
                            0 => "M&#46;E&#46; Martin"
                            1 => "S&#46; Fargion"
                            2 => "P&#46; Brissot"
                            3 => "B&#46; Pellat"
                            4 => "C&#46; Beaumont"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1998"
                        "volumen" => "91"
                        "paginaInicial" => "319"
                        "paginaFinal" => "323"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9414300"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            8 => array:3 [
              "identificador" => "bib0045"
              "etiqueta" => "9&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hereditary hyperferriti-nemia-cataract syndrome&#58; two novel mutations in the L-ferritin iron-responsive element"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "A&#46;D&#46; Munford"
                            1 => "T&#46; Vulliamy"
                            2 => "J&#46; Lindsay"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1998"
                        "volumen" => "91"
                        "paginaInicial" => "367"
                        "paginaFinal" => "368"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9414313"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            9 => array:3 [
              "identificador" => "bib0050"
              "etiqueta" => "10&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Description of a new mutation in the L-ferritin iron-responsi-ve element associated with hereditary hyperferritinemia-cataract syndrome in a spanish family"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:5 [
                            0 => "A&#46; Balas"
                            1 => "M&#46;J&#46; Avil&#233;s"
                            2 => "F&#46; Garc&#237;a-S&#225;nchez"
                            3 => "J&#46;L&#46; Vicario"
                            4 => "A&#46; Cervera"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1999"
                        "volumen" => "93"
                        "paginaInicial" => "4020"
                        "paginaFinal" => "4021"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/10383191"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            10 => array:3 [
              "identificador" => "bib0055"
              "etiqueta" => "11&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Function and regulation of transferrin and ferritin"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "P&#46; Ponka"
                            1 => "C&#46; Beaumont"
                            2 => "D&#46;R&#46; Richardson"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Semin Hematol"
                        "fecha" => "1998"
                        "volumen" => "35"
                        "paginaInicial" => "35"
                        "paginaFinal" => "54"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9460808"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            11 => array:3 [
              "identificador" => "bib0060"
              "etiqueta" => "12&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hemochromatosis and iron metabolism"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "T&#46;A&#46; Rouault"
                            1 => "M&#46;A&#46; Hediger"
                            2 => "N&#46;C&#46; Andrews"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:5 [
                        "tituloSerie" => "Gastroenterology"
                        "fecha" => "1999"
                        "volumen" => "116"
                        "paginaInicial" => "194"
                        "paginaFinal" => "195"
                      ]
                    ]
                  ]
                ]
              ]
            ]
            12 => array:3 [
              "identificador" => "bib0065"
              "etiqueta" => "13&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Thyroid hormo-ne modulates the interaction between iron regulatory pro-teins and the ferritin mRNA iron responsive element"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:4 [
                            0 => "P&#46;J&#46; Leedman"
                            1 => "A&#46;R&#46; Stein"
                            2 => "W&#46;W&#46; Chin"
                            3 => "J&#46;T&#46; Rogers"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:5 [
                        "tituloSerie" => "J Biol Chem"
                        "fecha" => "1996"
                        "volumen" => "12"
                        "paginaInicial" => "12017"
                        "paginaFinal" => "12023"
                      ]
                    ]
                  ]
                ]
              ]
            ]
            13 => array:3 [
              "identificador" => "bib0070"
              "etiqueta" => "14&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Hipertiroidismo&#44; otra causa de hiperferritinemia"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "M&#46; Rozman"
                            1 => "J&#46;L&#46; Vives Corrons"
                            2 => "C&#46; Rozman"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:4 [
                        "tituloSerie" => "Med Clin &#40;Barc&#41;"
                        "fecha" => "1992"
                        "volumen" => "99"
                        "paginaInicial" => "273"
                      ]
                    ]
                  ]
                ]
              ]
            ]
            14 => array:3 [
              "identificador" => "bib0075"
              "etiqueta" => "15&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Secondary iron overload disorders"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:1 [
                            0 => "S&#46;S&#46; Bottomley"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:5 [
                        "tituloSerie" => "Semin He-matol"
                        "fecha" => "1998"
                        "volumen" => "35"
                        "paginaInicial" => "77"
                        "paginaFinal" => "86"
                      ]
                    ]
                  ]
                ]
              ]
            ]
            15 => array:3 [
              "identificador" => "bib0080"
              "etiqueta" => "16&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Screening for hemochromatosis"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:2 [
                            0 => "C&#46;Q&#46; Edwards"
                            1 => "J&#46;P&#46; Kushner"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1056/NEJM199306033282208"
                      "Revista" => array:6 [
                        "tituloSerie" => "N Engl J Med"
                        "fecha" => "1993"
                        "volumen" => "328"
                        "paginaInicial" => "1616"
                        "paginaFinal" => "1620"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/8110209"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            16 => array:3 [
              "identificador" => "bib0085"
              "etiqueta" => "17&#46;"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Analysis of ferritins in lymphoblastoid cell lines and the lens of subjects with hereditary hyperferritinemia-cataract syndrome"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "S&#46; Levi"
                            1 => "D&#46; Girelli"
                            2 => "F&#46; Perrone"
                            3 => "M&#46; Pasti"
                            4 => "C&#46; Beaumont"
                            5 => "R&#46; Corrocher"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Blood"
                        "fecha" => "1998"
                        "volumen" => "91"
                        "paginaInicial" => "4180"
                        "paginaFinal" => "4187"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9596665"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
          ]
        ]
      ]
    ]
  ]
  "idiomaDefecto" => "es"
  "url" => "/16954033/0000005200000003/v1_201307051451/S169540330077336X/v1_201307051451/es/main.assets"
  "Apartado" => array:4 [
    "identificador" => "14441"
    "tipo" => "SECCION"
    "es" => array:2 [
      "titulo" => "Notas cl&#237;nicas"
      "idiomaDefecto" => true
    ]
    "idiomaDefecto" => "es"
  ]
  "PDF" => "https://static.elsevier.es/multimedia/16954033/0000005200000003/v1_201307051451/S169540330077336X/v1_201307051451/es/main.pdf?idApp=UINPBA00005H&text.app=https://analesdepediatria.org/"
  "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S169540330077336X?idApp=UINPBA00005H"
]
Información del artículo
ISSN: 16954033
Idioma original: Español
Datos actualizados diariamente
año/Mes Html Pdf Total
2024 Noviembre 8 16 24
2024 Octubre 53 62 115
2024 Septiembre 57 44 101
2024 Agosto 81 84 165
2024 Julio 86 59 145
2024 Junio 71 46 117
2024 Mayo 60 34 94
2024 Abril 90 52 142
2024 Marzo 58 52 110
2024 Febrero 61 49 110
2024 Enero 61 51 112
2023 Diciembre 56 27 83
2023 Noviembre 53 37 90
2023 Octubre 54 45 99
2023 Septiembre 57 36 93
2023 Agosto 41 26 67
2023 Julio 68 44 112
2023 Junio 43 31 74
2023 Mayo 75 35 110
2023 Abril 33 20 53
2023 Marzo 51 41 92
2023 Febrero 55 18 73
2023 Enero 41 25 66
2022 Diciembre 59 21 80
2022 Noviembre 75 57 132
2022 Octubre 48 50 98
2022 Septiembre 44 40 84
2022 Agosto 57 56 113
2022 Julio 26 47 73
2022 Junio 36 49 85
2022 Mayo 39 46 85
2022 Abril 37 55 92
2022 Marzo 70 52 122
2022 Febrero 42 37 79
2022 Enero 45 51 96
2021 Diciembre 44 55 99
2021 Noviembre 42 56 98
2021 Octubre 54 71 125
2021 Septiembre 54 52 106
2021 Agosto 31 36 67
2021 Julio 36 45 81
2021 Junio 43 76 119
2021 Mayo 46 44 90
2021 Abril 94 79 173
2021 Marzo 47 39 86
2021 Febrero 68 35 103
2021 Enero 68 47 115
2020 Diciembre 44 58 102
2020 Noviembre 28 36 64
2020 Octubre 55 21 76
2020 Septiembre 26 10 36
2020 Agosto 23 37 60
2020 Julio 34 46 80
2020 Junio 36 28 64
2020 Mayo 38 43 81
2020 Abril 38 29 67
2020 Marzo 31 24 55
2020 Febrero 23 23 46
2020 Enero 44 30 74
2019 Diciembre 33 44 77
2019 Noviembre 27 34 61
2019 Octubre 18 32 50
2019 Septiembre 48 45 93
2019 Agosto 37 32 69
2019 Julio 28 27 55
2019 Junio 29 52 81
2019 Mayo 38 89 127
2019 Abril 24 84 108
2019 Marzo 20 42 62
2019 Febrero 20 27 47
2019 Enero 17 24 41
2018 Diciembre 19 20 39
2018 Noviembre 30 30 60
2018 Octubre 52 33 85
2018 Septiembre 29 10 39
2018 Junio 1 0 1
2018 Mayo 7 0 7
2018 Abril 8 1 9
2018 Marzo 15 0 15
2018 Febrero 8 1 9
2018 Enero 14 1 15
2017 Diciembre 13 0 13
2017 Noviembre 18 0 18
2017 Octubre 13 0 13
2017 Septiembre 18 1 19
2017 Agosto 11 0 11
2017 Julio 22 2 24
2017 Junio 22 39 61
2017 Mayo 24 31 55
2017 Abril 25 7 32
2017 Marzo 25 37 62
2017 Febrero 12 36 48
2017 Enero 10 19 29
2016 Diciembre 23 11 34
2016 Noviembre 43 30 73
2016 Octubre 46 34 80
2016 Septiembre 64 31 95
2016 Agosto 57 35 92
2016 Julio 29 26 55
2016 Marzo 5 0 5
2016 Febrero 1 0 1
2016 Enero 1 0 1
2015 Diciembre 2 0 2
2015 Octubre 3 0 3
2015 Julio 9 0 9
2015 Junio 6 0 6
2015 Mayo 21 0 21
2015 Abril 9 0 9
2015 Marzo 6 0 6
2015 Febrero 6 0 6
2015 Enero 6 0 6
2014 Diciembre 7 0 7
2014 Noviembre 4 0 4
2014 Octubre 9 0 9
2014 Septiembre 11 0 11
2014 Agosto 7 0 7
2014 Julio 11 0 11
2014 Junio 18 0 18
2014 Mayo 20 0 20
2014 Abril 17 0 17
2014 Marzo 11 0 11
2014 Febrero 11 0 11
2014 Enero 17 0 17
2013 Diciembre 14 0 14
2013 Noviembre 9 0 9
2013 Octubre 12 0 12
2013 Septiembre 10 0 10
2013 Agosto 12 0 12
2013 Julio 3 0 3
2013 Junio 1 0 1
2013 Mayo 2 0 2
2013 Abril 2 0 2
2013 Marzo 8 0 8
2013 Febrero 9 0 9
2013 Enero 1 0 1
2012 Diciembre 1 0 1
2012 Noviembre 1 0 1
2012 Septiembre 4 0 4
2012 Agosto 3 0 3
2000 Marzo 3382 0 3382
Mostrar todo

Siga este enlace para acceder al texto completo del artículo

Idiomas
Anales de Pediatría
es en

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?