Trioche P - Search Results

1

Prenatal diagnosis of Crigler-Najjar syndrome type I by single-strand conformation polymorphism (SSCP).

Francoual J, Trioche P, Mokrani C, Seboui H, Khrouf N, Chalas J, Clement M, Capel L, Tachdjian G, Labrune P. Francoual J, et al. Among authors: trioche p. Prenat Diagn. 2002 Oct;22(10):914-6. doi: 10.1002/pd.443. Prenat Diagn. 2002. PMID: 12378576

2

Prenatal diagnosis of glycogen storage disease type Ia by restriction enzyme digestion.

Trioche P, Francoual J, Audibert F, Chalas J, Lindenbaum A, Odièvre M, Labrune P. Trioche P, et al. Prenat Diagn. 1998 Jun;18(6):629-31. Prenat Diagn. 1998. PMID: 9664612

3

Is a polymorphism of the apolipoprotein E gene associated with preeclampsia?

Francoual J, Audibert F, Trioche P, Chalas J, Capel L, Lindenbaum A, Labrune P, Frydman R. Francoual J, et al. Among authors: trioche p. Hypertens Pregnancy. 2002;21(2):127-33. doi: 10.1081/PRG-120004768. Hypertens Pregnancy. 2002. PMID: 12175441 Free article.

4

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

5

Identification of three novel mutations (Q54P, W70X and T108I) in the glucose-6-phosphatase gene of patients with glycogen storage disease type Ia. Mutation in brief no. 256. Online.

Trioche P, Francoual J, Chalas J, Capel L, Bernard O, Labrune P. Trioche P, et al. Hum Mutat. 1999;14(1):91. doi: 10.1002/(SICI)1098-1004(1999)14:1<91::AID-HUMU21>3.0.CO;2-B. Hum Mutat. 1999. PMID: 10447271

6

Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndrome.

Trioche P, Chalas J, Francoual J, Capel L, Lindenbaum A, Odièvre M, Labrune P. Trioche P, et al. Arch Dis Child. 1999 Oct;81(4):301-3. doi: 10.1136/adc.81.4.301. Arch Dis Child. 1999. PMID: 10490432 Free PMC article.

7

Genetic heterogeneity of glycogen storage disease type Ia in France: a study of 48 patients.

Trioche P, Francoual J, Chalas J, Capel L, Lindenbaum A, Odièvre M, Labrune P. Trioche P, et al. Hum Mutat. 2000 Nov;16(5):444. doi: 10.1002/1098-1004(200011)16:5<444::AID-HUMU10>3.0.CO;2-F. Hum Mutat. 2000. PMID: 11058903

8

[Genetic incidence of Gilbert's syndrome in France].

Le Bihan-Levaufre B, Francoual J, Chalas J, Trioche P, Capel L, Lindenbaum A, Labrune P. Le Bihan-Levaufre B, et al. Among authors: trioche p. Gastroenterol Clin Biol. 2001 May;25(5):557-8. Gastroenterol Clin Biol. 2001. PMID: 11521115 Free article. French. No abstract available.

9

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

10

[Neonatal jaundice. Physiopathology, etiology, diagnosis].

Trioche P, Labrune P. Trioche P, et al. Rev Prat. 1997 Nov 15;47(18):2081-4. Rev Prat. 1997. PMID: 9501629 French. No abstract available.

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