Odièvre M - Search Results

1

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: odievre m. 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

2

Tolerance to prolonged fasting in two children with type I glycogen storage disease.

Labrune P, Chalas J, Baussan C, Odièvre M. Labrune P, et al. Among authors: odievre m. J Inherit Metab Dis. 1993;16(6):1044-5. doi: 10.1007/BF00711524. J Inherit Metab Dis. 1993. PMID: 8127056 No abstract available.

3

Hepatocellular adenomas in glycogen storage disease type I and III: a series of 43 patients and review of the literature.

Labrune P, Trioche P, Duvaltier I, Chevalier P, Odièvre M. Labrune P, et al. Among authors: odievre m. J Pediatr Gastroenterol Nutr. 1997 Mar;24(3):276-9. doi: 10.1097/00005176-199703000-00008. J Pediatr Gastroenterol Nutr. 1997. PMID: 9138172 Review.

4

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: odievre m. Prenat Diagn. 1998 Jun;18(6):629-31. Prenat Diagn. 1998. PMID: 9664612

5

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

6

Increased levels of hemostatic proteins are independent of inflammation in glycogen storage disease type Ia.

Marfaing-Koka A, Wolf M, Boyer-Neumann C, Meyer D, Odievre M, Labrune P. Marfaing-Koka A, et al. Among authors: odievre m. J Pediatr Gastroenterol Nutr. 2003 Nov;37(5):566-70. doi: 10.1097/00005176-200311000-00011. J Pediatr Gastroenterol Nutr. 2003. PMID: 14581798

7

Serum concentrations of albumin, C-reactive protein, alpha 2-macroglobulin, prealbumin, fibronectin, fibrinogen, transferrin, and retinol binding protein in 55 patients with hepatic glycogen storage diseases.

Labrune P, Benattar C, Ammoury N, Chalas J, Lindenbaum A, Odièvre M. Labrune P, et al. Among authors: odievre m. J Pediatr Gastroenterol Nutr. 1994 Jan;18(1):41-4. doi: 10.1097/00005176-199401000-00007. J Pediatr Gastroenterol Nutr. 1994. PMID: 7510336

8

Moyamoya disease in a child with glycogen storage disease type Ia.

Goutières F, Bourgeois M, Trioche P, Demelier JF, Odievre M, Labrune P. Goutières F, et al. Among authors: odievre m. Neuropediatrics. 1997 Apr;28(2):133-4. doi: 10.1055/s-2007-973688. Neuropediatrics. 1997. PMID: 9208417

9

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: odievre m. 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.

10

Cardiomyopathy in glycogen-storage disease type III: clinical and echographic study of 18 patients.

Labrune P, Huguet P, Odievre M. Labrune P, et al. Among authors: odievre m. Pediatr Cardiol. 1991 Jul;12(3):161-3. doi: 10.1007/BF02238523. Pediatr Cardiol. 1991. PMID: 1876514

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