Síndrome de Crigler-Najjar: diagnóstico y tratamiento-Reference-Cited by-同舟云学术

Síndrome de Crigler-Najjar: diagnóstico y tratamiento

Published:2006-07 Issue:1 Volume:65 Page:73-78
ISSN:1695-4033
Container-title:Anales de Pediatría
language:es
Short-container-title:Anales de Pediatría

Author:

Lodoso Torrecilla B.,Palomo Atance E.,Camarena Grande C.,Díaz Fernández M.ªC.,Hierro Llanillo L.,de la Vega Bueno A.,Frauca Remacha E.,Muñoz Bartolo G.,Jara Vega P.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference19 articles.

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2. Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, Type-I;Bosma;Hepatology,1992

3. A mutation in bilirubin uridine 5’-diphosphate-glucuronosyltransferase isoform-1 causing Crigler-Najjar syndrome type-II;Bosma;Gastroenterology,1993

4. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert’s syndrome;Aono;Lancet,1995

5. The genetic basis of the reduced expresión of bilirubin UDP-glucuronosyltransferase 1 in Gilbert’s syndrome;Bosma;N Engl J Med,1995

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1. The added value of brain MR spectroscopy in children with Crigler-Najjar syndrome type-I: correlation with demographic, neurodevelopmental, and laboratory findings;The British Journal of Radiology;2023-03-01

2. Uridine diphosphate glucuronosyltransferase 1A1;Xenobiotica;2019-06-03

3. Glucuronidated bilirubin: Significantly increased in hepatic encephalopathy;Progress in Molecular Biology and Translational Science;2019

4. Bilirubin, a new therapeutic for kidney transplant?;Transplantation Reviews;2018-10

5. Fenobarbital en el síndrome de Crigler-Najjar tipo 1: una opción terapéutica;Anales de Pediatría;2016-08