Myara A - Search Results

1

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

Labrune P, Myara A, Hadchouel M, Ronchi F, Bernard O, Trivin F, Chowdhury NR, Chowdhury JR, Munnich A, Odièvre M. Labrune P, et al. Among authors: myara a. Hum Genet. 1994 Dec;94(6):693-7. doi: 10.1007/BF00206965. Hum Genet. 1994. PMID: 7989045

2

Crigler-Najjar type II disease inheritance: a family study.

Labrune P, Myara A, Hennion C, Gout JP, Trivin F, Odievre M. Labrune P, et al. Among authors: myara a. J Inherit Metab Dis. 1989;12(3):302-6. doi: 10.1007/BF01799221. J Inherit Metab Dis. 1989. PMID: 2515370

3

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

Labrune PH, Myara A, Francoual J, Trivin F, Odièvre M. Labrune PH, et al. Among authors: myara a. Pediatrics. 1992 Apr;89(4 Pt 2):768-70. Pediatrics. 1992. PMID: 1557275 No abstract available.

4

[Comparison of three methods evaluating the saturation of serum bilirubin transporters in children with type I Crigler Najjar disease].

Francoual J, Myara A, Trivin F, Leluc R, Odièvre M. Francoual J, et al. Among authors: myara a. Arch Fr Pediatr. 1990 Dec;47(10):721-3. Arch Fr Pediatr. 1990. PMID: 2082845 French.

5

Successful pregnancy in a Crigler-Najjar type I patient treated by phototherapy and semimonthly albumin infusions.

Gajdos V, Petit F, Trioche P, Mollet-Boudjemline A, Chauveaud A, Myara A, Trivin F, Francoual J, Labrune P. Gajdos V, et al. Among authors: myara a. Gastroenterology. 2006 Sep;131(3):921-4. doi: 10.1053/j.gastro.2006.07.005. Gastroenterology. 2006. PMID: 16952560 No abstract available.

6

Crigler-Najjar type II syndrome may result from several types and combinations of mutations in the UGT1A1 gene.

Petit F, Gajdos V, Capel L, Parisot F, Myara A, Francoual J, Labrune P. Petit F, et al. Among authors: myara a. Clin Genet. 2006 Jun;69(6):525-7. doi: 10.1111/j.1399-0004.2006.00616.x. Clin Genet. 2006. PMID: 16712705 No abstract available.

7

Association of a homozygous (TA)8 promoter polymorphism and a N400D mutation of UGT1A1 in a child with Crigler-Najjar type II syndrome.

Labrune P, Myara A, Chalas J, Le Bihan B, Capel L, Francoual J. Labrune P, et al. Among authors: myara a. Hum Mutat. 2002 Nov;20(5):399-401. doi: 10.1002/humu.10122. Hum Mutat. 2002. PMID: 12402338 No abstract available.

8

Crigler-Najjar syndrome type I in Tunisia may be associated with a founder effect related to the Q357R mutation within the UGT1 gene.

Francoual J, Rivierre A, Mokrani C, Khrouf N, Gottrand F, Myara A, Le Bihan B, Capel L, Lindenbaum A, Labrune P. Francoual J, et al. Among authors: myara a. Hum Mutat. 2002 May;19(5):570-1. doi: 10.1002/humu.10064. Hum Mutat. 2002. PMID: 11968090 No abstract available.

9

Correction of hyperbilirubinemia in gunn rats by surgical delivery of low doses of helper-dependent adenoviral vectors.

Schmitt F, Pastore N, Abarrategui-Pontes C, Flageul M, Myara A, Laplanche S, Labrune P, Podevin G, Nguyen TH, Brunetti-Pierri N. Schmitt F, et al. Among authors: myara a. Hum Gene Ther Methods. 2014 Jun;25(3):181-6. doi: 10.1089/hgtb.2013.236. Epub 2014 Apr 14. Hum Gene Ther Methods. 2014. PMID: 24593043

10

Successful gene therapy of the Gunn rat by in vivo neonatal hepatic gene transfer using murine oncoretroviral vectors.

Bellodi-Privato M, Aubert D, Pichard V, Myara A, Trivin F, Ferry N. Bellodi-Privato M, et al. Among authors: myara a. Hepatology. 2005 Aug;42(2):431-8. doi: 10.1002/hep.20794. Hepatology. 2005. PMID: 16025517

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