Petit FM - Search Results

1

A new mutation in the AFP gene responsible for a total absence of alpha feto-protein on second trimester maternal serum screening for Down syndrome.

Petit FM, Hébert M, Picone O, Brisset S, Maurin ML, Parisot F, Capel L, Benattar C, Sénat MV, Tachdjian G, Labrune P. Petit FM, et al. Eur J Hum Genet. 2009 Mar;17(3):387-90. doi: 10.1038/ejhg.2008.186. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854864 Free PMC article.

2

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.

3

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

4

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

5

Could sperm aneuploidy rate determination be used as a predictive test before intracytoplasmic sperm injection?

Petit FM, Frydman N, Benkhalifa M, Le Du A, Aboura A, Fanchin R, Frydman R, Tachdjian G. Petit FM, et al. J Androl. 2005 Mar-Apr;26(2):235-41. doi: 10.1002/j.1939-4640.2005.tb01090.x. J Androl. 2005. PMID: 15713829 Free article.

6

Glycogen storage disease type Ib without neutropenia generated by a novel splice-site mutation in the glucose-6-phosphate translocase gene.

Angaroni CJ, Labrune P, Petit F, Sastre D, Capra AE, Dodelson de Kremer R, Argaraña CE. Angaroni CJ, et al. Mol Genet Metab. 2006 May;88(1):96-9. doi: 10.1016/j.ymgme.2005.12.011. Epub 2006 Feb 21. Mol Genet Metab. 2006. PMID: 16490377

7

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.

8

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.

9

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.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

100 results

Search Page

Filters