Francoual J - Search Results

1

[Clinical, haemodynamic and genetic features of familial pulmonary arterial hypertension].

Sztrymf B, Francoual J, Sitbon O, Labrune P, Jambou M, Poüs C, Simonneau G, Humbert M. Sztrymf B, et al. Among authors: francoual j. Rev Mal Respir. 2004 Nov;21(5 Pt 1):909-15. doi: 10.1016/s0761-8425(04)71472-2. Rev Mal Respir. 2004. PMID: 15622337 French.

2

Urinary cGMP concentrations in severe primary pulmonary hypertension.

Bogdan M, Humbert M, Francoual J, Claise C, Duroux P, Simonneau G, Lindenbaum A. Bogdan M, et al. Among authors: francoual j. Thorax. 1998 Dec;53(12):1059-62. doi: 10.1136/thx.53.12.1059. Thorax. 1998. PMID: 10195079 Free PMC article.

3

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

4

[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: francoual j. Gastroenterol Clin Biol. 2001 May;25(5):557-8. Gastroenterol Clin Biol. 2001. PMID: 11521115 Free article. French. 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. Among authors: francoual j. 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

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: francoual j. J Inherit Metab Dis. 2000 Mar;23(2):107-12. doi: 10.1023/a:1005605513534. J Inherit Metab Dis. 2000. PMID: 10801051 Clinical Trial.

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. Among authors: francoual j. 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

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: francoual j. Pediatrics. 1992 Apr;89(4 Pt 2):768-70. Pediatrics. 1992. PMID: 1557275 No abstract available.

9

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. Among authors: francoual j. Prenat Diagn. 1998 Jun;18(6):629-31. Prenat Diagn. 1998. PMID: 9664612

10

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: francoual j. 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.

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