Información de la revista
Vol. 58. Núm. 2.
Páginas 168-173 (febrero 2003)
Compartir
Compartir
Descargar PDF
Más opciones de artículo
Vol. 58. Núm. 2.
Páginas 168-173 (febrero 2003)
Acceso a texto completo
Atresia de vías biliares
Visitas
111348
E. Donat Aliaga
Autor para correspondencia
ribes_car@qva.es

Correspondencia: Sección de Gastroenterología. Hospital Infantil La Fe.Avda. Campanar, 21. 46009 Valencia. España.
, B. Polo Miquel, C. Ribes-Koninckx
Sección de Gastroenterología. Hospital Infantil La Fe. Valencia. España.
Este artículo ha recibido
Información del artículo
El Texto completo está disponible en PDF
Bibliografía
[1.]
J. Vázquez, A.M. Hernández-Cano, J.A. Díez, J.R. Lilly.
Atresia de vías biliares. Estado actual.
An Esp Pediatr, 26 (1987), pp. 407-409
[2.]
P.W. Yoon, J.S. Bresee, R.S. Olney, L.M. James, M.J. Khoury.
Epidemiology of biliary atresia: A population-based study.
Pediatrics, 99 (1997), pp. 376-382
[3.]
P.F. Whitington.
Chronic Cholestasis of infancy.
Pediatr Clin North Am, 43 (1996), pp. 1-27
[4.]
I.D. D’Agata, W.F. Balistreri.
Evaluation of liver disease in the pediatric patient.
Pediatr Rev, 20 (1999), pp. 376-390
[5.]
M. Davenport, M. Savage, A.P. Mowat, E.R. Howard.
Biliary atresia splenic malformation syndromes: An etiologic and prognostic subgroup.
Surgery, 113 (1993), pp. 662-668
[6.]
H.H. A-Kader, M.J. Nowicki, K.I. Kuramoto, B. Baroudy, J.B. Zeldis, W.F. Balistreri.
Evaluation of the role of hepatitis C virus in biliary atresia.
Pediatr Infect Dis J, 13 (1994), pp. 657-658
[7.]
R.J. Sokol, C. Mack.
Etiopathogenesis of biliary atresia.
Semin Liver Dis, 21 (2001), pp. 517-524
[8.]
B. Fischler, B. Haglund, A. Hjern.
A population-based study on the incidence and possible pre-and perinatal etiologic risk factors of biliary atresia.
J Pediatr, 141 (2002), pp. 217-222
[9.]
J.M. Andres.
Neonatal hepatobiliary disorders.
Clin Perinatol, 23 (1996), pp. 321-352
[10.]
J.F. Fitzgerald.
Cholestatic disorders of infancy.
Pediatr Clin North Am, 35 (1988), pp. 357-375
[11.]
T.R. Silveria, F.M. Salzano, P.T. Donaldson, P.T. Donaldson, G. Mieli-Vergani, E.R. Howard.
Association between HLA and extrahepatic biliary atresia.
J Pediatr Gastroenterol Nutr, 16 (1993), pp. 114-117
[12.]
R.A. Schreiber, R.E. Kleinman.
Genetics, immunology and biliary atresia: An opening or a diversionα.
J Pediatr Gastroenterol Nutr, 16 (1993), pp. 111-113
[13.]
L. Camillus, M.D. Witzleben, D.A. Piccoli.
Extrahepatic bile ducts.
Pediatric gastrointestinal disease, 3rd ed, pp. 915-927
[14.]
K.P. Fung, S.P. Lau.
Gamma-glutamyl transpeptidase activity and its serial measurament in differentation between extrahepatic biliary atresia and neonatal hepatitis.
J Pediatr Gastroenterol Nutr, 4 (1985), pp. 208-213
[15.]
G. Maggiore, O. Bernard, M. Hadchouel, A. Lemmonier, D. Alagille.
Diagnostic value of serum gamma-glutamyl transpeptidase activity in liver diseases in children.
J Pediatr Gastroenterol Nutr, 12 (1991), pp. 21-26
[16.]
R.P. Altman, S. Abramson.
Potential errors in the diagnosis and surgical management of neonatal jaundice.
J Pediatr Surg, 20 (1985), pp. 529-534
[17.]
S.O. Choi, W.H. Park, H.J. Lee.
Ultrasonographic Triangular Cord: the most definitive finding for noninvaisve diagnosis of extrahepatic.
Eur J Pediatr Surg, 8 (1998), pp. 12-16
[18.]
W.H. Park, S.O. Choi, H.J. Lee, S.P. Kim, S.K. Zeon, S.L. Lee.
A new diagnostic approach to biliary atresia with emphasis on the ultrasonographic triangular cord sign: comparison ultrasonography, hepatobiliary scintigraphy, and liver need biopsy in the evaluation of infantile cholestasis.
J Pediatr Surg, 32 (1997), pp. 1555-1559
[19.]
A.G. Manolaki, V.F. Larcher, A.P. Mowat, J.J. Barrett, B. Portmann, E.R. Howard.
The prelaparotomy diagnosis of extrahepatic biliary atresia.
Arch Dis Child, 58 (1983), pp. 591-594
[20.]
G. Azar, D. Benecck, B. Lane, J. Markowitz, F. Daum, E. Kahn.
Atypical morphologic presentation of biliary atresia and value of serial liver biopsies.
J Pediatr Gastroenterol Nutr, 34 (2002), pp. 212-215
[21.]
M.B. Heyman, H.L. Shapiro, M.M. Thaler.
Endoscopic retrograde cholangiography in the diagnosis of biliary malformations in children.
Gastrointest Endosc, 34 (1988), pp. 449-453
[22.]
M. Guelrud, D. Jean, S. Mendoza, J. Plaz, P. Torres.
ERCP in the diagnosis of extrahepatic biliary atresia.
Gastrointest Endosc, 37 (1991), pp. 522-526
[23.]
S. Logan, A. Stanton.
Screening for biliary atresia.
Lancet, 342 (1993), pp. 256
[24.]
J.R. Lilly.
The surgery of “correctable“ biliary atresia.
J Pediatr Surg, 20 (1985), pp. 522-525
[25.]
K. Suruga, S. Tsunoda, E. Deguchi, K. Kimura, T. Miyano.
The future role of hepatic portoenterostomy as treatment of biliary atresia.
J Pediatr Surg, 20 (1992), pp. 707-709
[26.]
M. Oh, M. Hobeldin, T. Chen, D.W. Thomas, J.B. Atkinson.
The kasai procedure in the treatment of biliary atresia.
J Pediatr Surg, 30 (1995), pp. 1077-1081
[27.]
R. Emblem, Shake, I. Monclan.
Progress in the treatment of biliary atresia: A plea for surgical intervention within the first two months of life in infants with persistent cholestasis.
Acta Pediatr, 82 (1993), pp. 971-974
[28.]
V. Martinez, J. Boix-Ochoa, J. Lloret, J. Broto.
Paediatric liver transplantation: Life after portoenterostomy in biliary atresia.
J Pediatr Surg, 27 (1992), pp. 830-832
[29.]
P.J. Mc Kiernan, A.J. Backer, D.A. Kelly.
The frecuency and outcome of biliary atresia in the UK and Ireland.
[30.]
J.N. Lin, K.L. Wang, J.H. Chuang.
The efficacy of Kasai operation for biliary atresia: A single institutional experience.
J Pediatr Surg, 20 (1992), pp. 704-706
[31.]
R.W. DeConti, R.D. Craver, G.W. Willis, C.B. Hill, D.H. Hayes, R.M. Arensman.
Extrahepatic biliary atresia: From diagnosis to liver transplantation.
Pediatr Surg Int, 7 (1992), pp. 337-340
[32.]
T. Muraji, Y. Higgashimoto.
The inproved outlook of biliary atresia with corticosteroid therapy.
J Pediatr Surg, 9 (1997), pp. 1103-1106
[33.]
J. Manzanares, P. Urruzuno, E. Medina.
Tratamiento médico del niño con enfermedad colestática crónica. Soporte nutricional y tratamiento sustitutivo.
An Esp Pediatr, 116 (1998), pp. 18-21
[34.]
V. Ramaccioni, H.E. Soriano, R. Arumugam, W.J. Klish.
Nutritional aspects of chronic liver disease and liver transplantation in children.
J Pediatr Gastroenterol Nutr, 30 (2000), pp. 361-367
[35.]
P. Vajro, M. Couturier, F. Lemmonier, M. Odievre.
Effects of post-operative cholerstyramine and phenobarbital administration on bile flow restoration in infants with extrahepatic biliary atresia.
J Pediatr Surg, 21 (1986), pp. 36235-36236
[36.]
E.A. Jones, N.V. Bregaza.
The pruritus of colestasis.
Hepatology, 29 (1999), pp. 1003-1006
[37.]
A.F. Hofmann.
Cholestatic liver disease: pathophysiology and therapeutic options.
Liver, 22 (2002), pp. 14-19
[38.]
B. Yerushalmi, R.J. Sokol, M.R. Narkewicz, D. Smith, F.M. Karrer.
Use of rifampicin for severe pruritus in children with cronic cholestasis.
J Pediatr Gastroenterol Nutr, 29 (1999), pp. 442-447
[39.]
C. Steiner, S. Mitzner.
Experiences with MARS liver support therapy in liver failure: Analysis of 176 patients of the International MARS Registry.
Liver, 2 (2002), pp. 20-25
[40.]
C. Ribes-Koninckx, B. Polo, R. Sanchis, E. Donat.
Application of an extracorporeal hepatic support device (MARS) in pediatric patients.
J Paediatr Gastroenterol Nutr, 34 (2002), pp. 440
Copyright © 2003. Asociación Española de Pediatría
Descargar PDF
Idiomas
Anales de Pediatría
Opciones de artículo
Herramientas
es en

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

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