array:23 [ "pii" => "S1695403301775534" "issn" => "16954033" "doi" => "10.1016/S1695-4033(01)77553-4" "estado" => "S300" "fechaPublicacion" => "2001-04-01" "aid" => "77553" "copyright" => "Asociación Española de Pediatría" "copyrightAnyo" => "2001" "documento" => "article" "crossmark" => 0 "subdocumento" => "cor" "cita" => "An Pediatr (Barc). 2001;54:411-2" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 4674 "formatos" => array:3 [ "EPUB" => 74 "HTML" => 3647 "PDF" => 953 ] ] "itemSiguiente" => array:18 [ "pii" => "S1695403301775546" "issn" => "16954033" "doi" => "10.1016/S1695-4033(01)77554-6" "estado" => "S300" "fechaPublicacion" => "2001-04-01" "aid" => "77554" "copyright" => "Asociación Española de Pediatría" "documento" => "simple-article" "crossmark" => 0 "subdocumento" => "cor" "cita" => "An Pediatr (Barc). 2001;54:412-3" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 2071 "formatos" => array:3 [ "EPUB" => 52 "HTML" => 1607 "PDF" => 412 ] ] "es" => array:7 [ "idiomaDefecto" => true "titulo" => "A vueltas con el oxígeno puro" "tienePdf" => "es" "tieneTextoCompleto" => 0 "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "412" "paginaFinal" => "413" ] ] "contienePdf" => array:1 [ "es" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "V. Modesto, J. Pantoja, S. Vidal" "autores" => array:3 [ 0 => array:2 [ "nombre" => "V." "apellidos" => "Modesto" ] 1 => array:2 [ "nombre" => "J." "apellidos" => "Pantoja" ] 2 => array:2 [ "nombre" => "S." "apellidos" => "Vidal" ] ] ] ] ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403301775546?idApp=UINPBA00005H" "url" => "/16954033/0000005400000004/v1_201307051547/S1695403301775546/v1_201307051547/es/main.assets" ] "itemAnterior" => array:18 [ "pii" => "S1695403301775522" "issn" => "16954033" "doi" => "10.1016/S1695-4033(01)77552-2" "estado" => "S300" "fechaPublicacion" => "2001-04-01" "aid" => "77552" "copyright" => "Asociación Española de Pediatría" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "An Pediatr (Barc). 2001;54:409-10" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 5370 "formatos" => array:3 [ "EPUB" => 66 "HTML" => 4841 "PDF" => 463 ] ] "es" => array:7 [ "idiomaDefecto" => true "titulo" => "Defecto vertebral múltiple con otras anomalías acompañantes" "tienePdf" => "es" "tieneTextoCompleto" => 0 "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "409" "paginaFinal" => "410" ] ] "contienePdf" => array:1 [ "es" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "E. García Barrecheguren, M. Alfonso Olmos, J.L. Beguiristáin Gúrpide" "autores" => array:3 [ 0 => array:2 [ "nombre" => "E." "apellidos" => "García Barrecheguren" ] 1 => array:2 [ "nombre" => "M." "apellidos" => "Alfonso Olmos" ] 2 => array:2 [ "nombre" => "J.L." "apellidos" => "Beguiristáin Gúrpide" ] ] ] ] ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403301775522?idApp=UINPBA00005H" "url" => "/16954033/0000005400000004/v1_201307051547/S1695403301775522/v1_201307051547/es/main.assets" ] "es" => array:8 [ "idiomaDefecto" => true "titulo" => "Cromosomopatía 13 en anillo y déficit congénito de factores de coagulación" "tieneTextoCompleto" => 0 "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "411" "paginaFinal" => "412" ] ] "autores" => array:1 [ 0 => array:3 [ "autoresLista" => "M.<span class="elsevierStyleSup">a</span>Y. Ruiz del Prado, J. Alfonso Landa, C. Cristóbal Navas, J. Blázquez Regidor, J.A. Pérez Marrodán, A. Martín Nuño" "autores" => array:6 [ 0 => array:3 [ "nombre" => "M.<span class="elsevierStyleSup">a</span>Y." "apellidos" => "Ruiz del Prado" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 1 => array:3 [ "nombre" => "J." "apellidos" => "Alfonso Landa" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 2 => array:3 [ "nombre" => "C." "apellidos" => "Cristóbal Navas" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 3 => array:3 [ "nombre" => "J." "apellidos" => "Blázquez Regidor" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 4 => array:3 [ "nombre" => "J.A." "apellidos" => "Pérez Marrodán" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 5 => array:3 [ "nombre" => "A." "apellidos" => "Martín Nuño" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] ] "afiliaciones" => array:2 [ 0 => array:3 [ "entidad" => "Servicios de Pediatría. Complejo Hospitalario San Millán-San Pedro." "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Servicio de Hematología. Complejo Hospitalario San Millán-San Pedro. Logroño." "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "bibliografia" => array:2 [ "titulo" => "Bibliografía" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:9 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Monosomía r(13): a propósito de una nueva observación." "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:6 [ 0 => "M. Cuadrado" 1 => "C. Boldova" 2 => "S. Carrasco" 3 => "S. Martínez" 4 => "J. López-Pisón" 5 => "A. Baldellou" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "An Esp Ped" "fecha" => "2000" "volumen" => "53" "paginaInicial" => "592" "paginaFinal" => "595" ] ] ] ] ] ] 1 => array:3 [ "identificador" => "bib0010" "etiqueta" => "2." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Ultrasonographic prenatal diagnosis of the 13q-syndrome." "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:6 [ 0 => "J. Santolaya" 1 => "M.M. McCorquodale" 2 => "W. Torres" 3 => "W.J. Meyer" 4 => "D. Gauthier" 5 => "D. Lemery" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Fetal Diagn Ther" "fecha" => "1993" "volumen" => "8" "paginaInicial" => "261" "paginaFinal" => "267" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/8260080" "web" => "Medline" ] ] ] ] ] ] ] ] 2 => array:3 [ "identificador" => "bib0015" "etiqueta" => "3." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Structural genes of coagulation factors VII and X located on 13q34." "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:6 [ 0 => "S. Gilgenkrantz" 1 => "M.E. Briquel" 2 => "E. Andre" 3 => "P. Alexandre" 4 => "P. Jalbert" 5 => "B. Le Marec" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Ann Genet" "fecha" => "1986" "volumen" => "29" "paginaInicial" => "32" "paginaFinal" => "35" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/3487272" "web" => "Medline" ] ] ] ] ] ] ] ] 3 => array:3 [ "identificador" => "bib0020" "etiqueta" => "4." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Ring Chromosome 13 in a child with minor dysmorphic features." "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "R.S. Verma" 1 => "H. Dosik" 2 => "I.H. Chowdhry" 3 => "R.C. Jhaveri" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Am J Dis Child" "fecha" => "1978" "volumen" => "132" "paginaInicial" => "1018" "paginaFinal" => "1021" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/717293" "web" => "Medline" ] ] ] ] ] ] ] ] 4 => array:3 [ "identificador" => "bib0025" "etiqueta" => "5." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Hereditary deficiencies of clotting factors VII and X associated with carotid-body tumours." "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "A.J. Kroll" 1 => "B. Alexander" 2 => "F. Cochios" 3 => "L. Pechet" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1056/NEJM196401022700102" "Revista" => array:6 [ "tituloSerie" => "N Engl J Med" "fecha" => "1964" "volumen" => "270" "paginaInicial" => "6" "paginaFinal" => "13" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/14062129" "web" => "Medline" ] ] ] ] ] ] ] ] 5 => array:3 [ "identificador" => "bib0030" "etiqueta" => "6." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Deficiency coagulation factors VII ad X associated with deletion of chromosome 13 (q34). Evidence from two cases with 46 XY, t (13;Y) (q11; q34)." "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "R.A. Pfeiffer" 1 => "R. Ott" 2 => "S. Gilgenkrantz" 3 => "P. Alexandre" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Hum Genet" "fecha" => "1982" "volumen" => "62" "paginaInicial" => "358" "paginaFinal" => "360" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/6985471" "web" => "Medline" ] ] ] ] ] ] ] ] 6 => array:3 [ "identificador" => "bib0035" "etiqueta" => "7." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Frequent association of factors VII defects with other clotting disorders." "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "A. Girolami" 1 => "M.Y. Sartori" 2 => "P. Zerbinati" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "Blood Coagul Fibrinolysis" "fecha" => "1992" "volumen" => "13" "paginaInicial" => "829" "paginaFinal" => "831" ] ] ] ] ] ] 7 => array:3 [ "identificador" => "bib0040" "etiqueta" => "8." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Activity and antigen of coagulation factors VII and X, in five patient with abnormal chromosome 13." "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "Y. Fukushima" 1 => "Y. Kuroki" 2 => "A. Lizuka" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "Jpn J Hum Genet" "fecha" => "1987" "volumen" => "32" "paginaInicial" => "91" "paginaFinal" => "96" ] ] ] ] ] ] 8 => array:3 [ "identificador" => "bib0045" "etiqueta" => "9." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Déficit congénito de factor VII y X en un paciente portador de un cromosoma 13 en anillo." "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:6 [ 0 => "M. Tapia" 1 => "P. Vicente" 2 => "A. Rubio" 3 => "C. Aguilar" 4 => "F. Lucia" 5 => "M. Torres" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "Rev Esp Pediatr" "fecha" => "1996" "volumen" => "52" "paginaInicial" => "279" "paginaFinal" => "281" ] ] ] ] ] ] ] ] ] ] ] "idiomaDefecto" => "es" "url" => "/16954033/0000005400000004/v1_201307051547/S1695403301775534/v1_201307051547/es/main.assets" "Apartado" => array:4 [ "identificador" => "14233" "tipo" => "SECCION" "es" => array:2 [ "titulo" => "Cartas al director" "idiomaDefecto" => true ] "idiomaDefecto" => "es" ] "PDF" => "https://static.elsevier.es/multimedia/16954033/0000005400000004/v1_201307051547/S1695403301775534/v1_201307051547/es/main.pdf?idApp=UINPBA00005H&text.app=https://analesdepediatria.org/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1695403301775534?idApp=UINPBA00005H" ]
Información de la revista
Vol. 54. Núm. 4.
Páginas 411-412 (abril 2001)
Vol. 54. Núm. 4.
Páginas 411-412 (abril 2001)
Acceso a texto completo
Cromosomopatía 13 en anillo y déficit congénito de factores de coagulación
Visitas
8356
Este artículo ha recibido
Información del artículo
El Texto completo está disponible en PDF
Bibliografía
[1.]
M. Cuadrado, C. Boldova, S. Carrasco, S. Martínez, J. López-Pisón, A. Baldellou.
Monosomía r(13): a propósito de una nueva observación..
An Esp Ped, 53 (2000), pp. 592-595
[2.]
J. Santolaya, M.M. McCorquodale, W. Torres, W.J. Meyer, D. Gauthier, D. Lemery.
Ultrasonographic prenatal diagnosis of the 13q-syndrome..
Fetal Diagn Ther, 8 (1993), pp. 261-267
[3.]
S. Gilgenkrantz, M.E. Briquel, E. Andre, P. Alexandre, P. Jalbert, B. Le Marec.
Structural genes of coagulation factors VII and X located on 13q34..
Ann Genet, 29 (1986), pp. 32-35
[4.]
R.S. Verma, H. Dosik, I.H. Chowdhry, R.C. Jhaveri.
Ring Chromosome 13 in a child with minor dysmorphic features..
Am J Dis Child, 132 (1978), pp. 1018-1021
[5.]
A.J. Kroll, B. Alexander, F. Cochios, L. Pechet.
Hereditary deficiencies of clotting factors VII and X associated with carotid-body tumours..
N Engl J Med, 270 (1964), pp. 6-13
[6.]
R.A. Pfeiffer, R. Ott, S. Gilgenkrantz, P. Alexandre.
Deficiency coagulation factors VII ad X associated with deletion of chromosome 13 (q34). Evidence from two cases with 46 XY, t (13;Y) (q11; q34)..
Hum Genet, 62 (1982), pp. 358-360
[7.]
A. Girolami, M.Y. Sartori, P. Zerbinati.
Frequent association of factors VII defects with other clotting disorders..
Blood Coagul Fibrinolysis, 13 (1992), pp. 829-831
[8.]
Y. Fukushima, Y. Kuroki, A. Lizuka.
Activity and antigen of coagulation factors VII and X, in five patient with abnormal chromosome 13..
Jpn J Hum Genet, 32 (1987), pp. 91-96
[9.]
M. Tapia, P. Vicente, A. Rubio, C. Aguilar, F. Lucia, M. Torres.
Déficit congénito de factor VII y X en un paciente portador de un cromosoma 13 en anillo..
Rev Esp Pediatr, 52 (1996), pp. 279-281
Copyright © 2001. Asociación Española de Pediatría