Fenobarbital en el síndrome de Crigler-Najjar tipo 1: una opción terapéutica
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Published in | Anales de pediatría (Barcelona, Spain : 2003) Vol. 85; no. 2; pp. 115 - 116 |
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Main Authors | , , , |
Format | Journal Article |
Language | Spanish |
Published |
Elsevier España, S.L.U
01.08.2016
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Subjects | |
Online Access | Get full text |
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Author | López González, María Fernanda Ibáñez Alcalde, María Mercedes Cañabate Reche, Francisco Rubio Gómez, Irene |
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Cites_doi | 10.1016/S0925-4439(98)00030-1 10.1157/13090900 10.1002/humu.21133 10.1016/j.anpedi.2015.11.001 |
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DocumentTitleAlternate | Phenobarbital in Crigler-Najjar syndrome type 1: A therapeutic option |
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References | Lodoso, Palomo, Camarena, Díaz, Hierro, de la Vega (bib0040) 2006; 65 De la Rosa, Matesanz (bib0025) 2015; 83 Ciotti, Chen, Rubaltelli, Owens (bib0035) 1998; 1407 Sneitz, Bakker, de Knegt, Halley, Finel, Bosma (bib0030) 2010; 31 De la Rosa (10.1016/j.anpedi.2016.03.017_bib0025) 2015; 83 Ciotti (10.1016/j.anpedi.2016.03.017_bib0035) 1998; 1407 Sneitz (10.1016/j.anpedi.2016.03.017_bib0030) 2010; 31 Lodoso (10.1016/j.anpedi.2016.03.017_bib0040) 2006; 65 |
References_xml | – volume: 83 year: 2015 ident: bib0025 article-title: El trasplante hepático e intestinal en población pediátrica publication-title: An Pediatr contributor: fullname: Matesanz – volume: 65 start-page: 73 year: 2006 end-page: 78 ident: bib0040 article-title: Síndrome de Crigler-Najjar: diagnóstico y tratamiento publication-title: An Pediatr contributor: fullname: de la Vega – volume: 1407 start-page: 40 year: 1998 end-page: 50 ident: bib0035 article-title: Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosltransferase gene cause Crigler-Najjar type I disease publication-title: Biochin Biophys Acta contributor: fullname: Owens – volume: 31 start-page: 52 year: 2010 end-page: 59 ident: bib0030 article-title: Crigler-Najjar syndrome in the Netherlands: Identification of four novel UGT1A1 alleles, genotype-phenotype correlation, and functional analysis of 10 missense mutants publication-title: Hum Mutat contributor: fullname: Bosma – volume: 1407 start-page: 40 year: 1998 ident: 10.1016/j.anpedi.2016.03.017_bib0035 article-title: Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosltransferase gene cause Crigler-Najjar type I disease publication-title: Biochin Biophys Acta doi: 10.1016/S0925-4439(98)00030-1 contributor: fullname: Ciotti – volume: 65 start-page: 73 year: 2006 ident: 10.1016/j.anpedi.2016.03.017_bib0040 article-title: Síndrome de Crigler-Najjar: diagnóstico y tratamiento publication-title: An Pediatr doi: 10.1157/13090900 contributor: fullname: Lodoso – volume: 31 start-page: 52 year: 2010 ident: 10.1016/j.anpedi.2016.03.017_bib0030 article-title: Crigler-Najjar syndrome in the Netherlands: Identification of four novel UGT1A1 alleles, genotype-phenotype correlation, and functional analysis of 10 missense mutants publication-title: Hum Mutat doi: 10.1002/humu.21133 contributor: fullname: Sneitz – volume: 83 year: 2015 ident: 10.1016/j.anpedi.2016.03.017_bib0025 article-title: El trasplante hepático e intestinal en población pediátrica publication-title: An Pediatr doi: 10.1016/j.anpedi.2015.11.001 contributor: fullname: De la Rosa |
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Title | Fenobarbital en el síndrome de Crigler-Najjar tipo 1: una opción terapéutica |
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