Capel L - Search Results

1

Apolipoprotein E polymorphism and serum concentrations in patients with glycogen storage disease type Ia.

Trioche P, Francoual J, Capel L, Odièvre M, Lindenbaum A, Labrune P. Trioche P, et al. Among authors: capel l. J Inherit Metab Dis. 2000 Mar;23(2):107-12. doi: 10.1023/a:1005605513534. J Inherit Metab Dis. 2000. PMID: 10801051 Clinical Trial.

2

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: capel l. Hypertens Pregnancy. 2002;21(2):127-33. doi: 10.1081/PRG-120004768. Hypertens Pregnancy. 2002. PMID: 12175441 Free article.

3

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. Among authors: capel l. 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

4

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. Among authors: capel l. 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

5

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. Among authors: capel l. J Inherit Metab Dis. 2004;27(5):621-3. doi: 10.1023/b:boli.0000042987.43395.c6. J Inherit Metab Dis. 2004. PMID: 15669677

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. Among authors: capel l. 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

[Refinement and role of the diagnosis of Gilbert disease with molecular biology].

Le Bihan-Levaufre B, Francoual J, Labrune P, Chalas J, Capel L, Lindenbaum A. Le Bihan-Levaufre B, et al. Among authors: capel l. Ann Biol Clin (Paris). 2001 Jan-Feb;59(1):61-6. Ann Biol Clin (Paris). 2001. PMID: 11174102 Free article. Review. French.

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: capel l. Gastroenterol Clin Biol. 2001 May;25(5):557-8. Gastroenterol Clin Biol. 2001. PMID: 11521115 Free article. French. No abstract available.

9

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: capel l. Prenat Diagn. 2002 Oct;22(10):914-6. doi: 10.1002/pd.443. Prenat Diagn. 2002. PMID: 12378576

10

Oxidized low-density lipoprotein induces the production of interleukin-8 by endothelial cells.

Claise C, Edeas M, Chalas J, Cockx A, Abella A, Capel L, Lindenbaum A. Claise C, et al. Among authors: capel l. FEBS Lett. 1996 Dec 2;398(2-3):223-7. doi: 10.1016/s0014-5793(96)01255-0. FEBS Lett. 1996. PMID: 8977111 Free article.

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