Literature DB >> 1557275

Cerebellar symptoms as the presenting manifestations of bilirubin encephalopathy in children with Crigler-Najjar type I disease.

P H Labrune1, A Myara, J Francoual, F Trivin, M Odièvre.   

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Year:  1992        PMID： 1557275

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  4 in total

1.  Successful plasmapheresis for acute and severe unconjugated hyperbilirubinemia in a child with crigler najjar type I syndrome.

Authors:  Anne Laure Sellier; Philippe Labrune; Theresa Kwon; Alix Mollet Boudjemline; Georges Deschènes; Vincent Gajdos
Journal:  JIMD Rep       Date:  2011-09-06

2.  Auxiliary partial orthotopic liver transplantation for Crigler-Najjar syndrome type I.

Authors:  M Rela; P Muiesan; H Vilca-Melendez; A Dhawan; A Baker; G Mieli-Vergani; N D Heaton
Journal:  Ann Surg       Date:  1999-04       Impact factor: 12.969

3.  Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 cases.

Authors:  P Labrune; A Myara; M Hadchouel; F Ronchi; O Bernard; F Trivin; N R Chowdhury; J R Chowdhury; A Munnich; M Odièvre
Journal:  Hum Genet       Date:  1994-12       Impact factor: 4.132

4.  A translationally optimized AAV-UGT1A1 vector drives safe and long-lasting correction of Crigler-Najjar syndrome.

Authors:  Giuseppe Ronzitti; Giulia Bortolussi; Remco van Dijk; Fanny Collaud; Severine Charles; Christian Leborgne; Patrice Vidal; Samia Martin; Bernard Gjata; Marcelo Simon Sola; Laetitia van Wittenberghe; Alban Vignaud; Philippe Veron; Piter J Bosma; Andres F Muro; Federico Mingozzi
Journal:  Mol Ther Methods Clin Dev       Date:  2016-07-20       Impact factor: 6.698
  4 in total

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