Petit FM - Search Results

1

Further evidence that the UGT1A1*28 allele is not associated with coronary heart disease: The ECTIM Study.

Gajdos V, Petit FM, Perret C, Mollet-Boudjemline A, Colin P, Capel L, Nicaud V, Evans A, Arveiler D, Parisot F, Francoual J, Genin E, Cambien F, Labrune P. Gajdos V, et al. Among authors: petit fm. Clin Chem. 2006 Dec;52(12):2313-4. doi: 10.1373/clinchem.2006.078667. Clin Chem. 2006. PMID: 17138857 No abstract available.

2

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. 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.

3

Comments on seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia by D'Apolito et al.

Petit FM, Hébert M, Gajdos V, Mollet-Boudjemline A, Labrune P. Petit FM, et al. Haematologica. 2007 Jul;92(7):e80. doi: 10.3324/haematol.11817. Haematologica. 2007. PMID: 17726772 Free article. No abstract available.

4

Large deletion in UGT1A1 gene encompassing the promoter and the exon 1 responsible for Crigler-Najjar type I syndrome.

Petit FM, Hébert M, Gajdos V, Capel L, M'Rad R, Labrune P. Petit FM, et al. Haematologica. 2008 Oct;93(10):1590-1. doi: 10.3324/haematol.13295. Epub 2008 Aug 12. Haematologica. 2008. PMID: 18698077 Free article. No abstract available.

5

Allelic heterogeneity of Crigler-Najjar type I syndrome: a study of 24 cases.

Petit FM, Gajdos V, Francoual J, Capel L, Parisot F, Poüs C, Labrune P. Petit FM, et al. Clin Genet. 2004 Dec;66(6):571-2. doi: 10.1111/j.1399-0004.2004.00371.x. Clin Genet. 2004. PMID: 15521991 No abstract available.

6

The Tunisian population history through the Crigler-Najjar type I syndrome.

Petit FM, Bézieau S, Gajdos V, Parisot F, Scoul C, Capel L, Stozinic V, Khrouf N, M'Rad R, Koshy A, Mollet-Boudjemline A, Francoual J, Labrune P. Petit FM, et al. Eur J Hum Genet. 2008 Jul;16(7):848-53. doi: 10.1038/sj.ejhg.5201989. Epub 2008 Jan 16. Eur J Hum Genet. 2008. PMID: 18197191

7

Allelic heterogeneity of glycogen storage disease type Ib in French patients: a study of 11 cases.

Trioche P, Petit F, Francoual J, Gajdos V, Capel L, Poüs C, Labrune P. Trioche P, et al. J Inherit Metab Dis. 2004;27(5):621-3. doi: 10.1023/b:boli.0000042987.43395.c6. J Inherit Metab Dis. 2004. PMID: 15669677

8

Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.

Petit FM, Gajdos V, Parisot F, Capel L, Aboura A, Lachaux A, Tachdjian G, Poüs C, Labrune P. Petit FM, et al. Eur J Hum Genet. 2005 Mar;13(3):278-82. doi: 10.1038/sj.ejhg.5201342. Eur J Hum Genet. 2005. PMID: 15586176

9

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. Gastroenterology. 2006 Sep;131(3):921-4. doi: 10.1053/j.gastro.2006.07.005. Gastroenterology. 2006. PMID: 16952560 No abstract available.

10

Glucose-6-phosphatase deficiency.

Froissart R, Piraud M, Boudjemline AM, Vianey-Saban C, Petit F, Hubert-Buron A, Eberschweiler PT, Gajdos V, Labrune P. Froissart R, et al. Orphanet J Rare Dis. 2011 May 20;6:27. doi: 10.1186/1750-1172-6-27. Orphanet J Rare Dis. 2011. PMID: 21599942 Free PMC article. Review.

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