Labrune P - Search Results

1

Severe pulmonary arterial hypertension in type 1 glycogen storage disease.

Humbert M, Labrune P, Simonneau G. Humbert M, et al. Among authors: labrune p. Eur J Pediatr. 2002 Oct;161 Suppl 1:S93-6. doi: 10.1007/s00431-002-1012-y. Epub 2002 Jul 31. Eur J Pediatr. 2002. PMID: 12373580

2

Pulmonary arterial hypertension and type-I glycogen-storage disease: the serotonin hypothesis.

Humbert M, Labrune P, Sitbon O, Le Gall C, Callebert J, Hervé P, Samuel D, Machado R, Trembath R, Drouet L, Launay JM, Simonneau G. Humbert M, et al. Among authors: labrune p. Eur Respir J. 2002 Jul;20(1):59-65. doi: 10.1183/09031936.02.00258702. Eur Respir J. 2002. PMID: 12166582 Free article.

3

[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: labrune p. 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.

4

Contraception and pregnancy in women affected by glycogen storage diseases.

Mairovitz V, Labrune P, Fernandez H, Audibert F, Frydman R. Mairovitz V, et al. Among authors: labrune p. Eur J Pediatr. 2002 Oct;161 Suppl 1:S97-101. doi: 10.1007/s00431-002-1013-x. Epub 2002 Sep 4. Eur J Pediatr. 2002. PMID: 12373581 Review.

5

Glycogen storage disease type I: indications for liver and/or kidney transplantation.

Labrune P. Labrune P. Eur J Pediatr. 2002 Oct;161 Suppl 1:S53-5. doi: 10.1007/s00431-002-1004-y. Epub 2002 Jul 19. Eur J Pediatr. 2002. PMID: 12373572 Review.

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: labrune p. 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

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: labrune p. J Pediatr Gastroenterol Nutr. 2003 Nov;37(5):566-70. doi: 10.1097/00005176-200311000-00011. J Pediatr Gastroenterol Nutr. 2003. PMID: 14581798

8

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. J Pediatr Gastroenterol Nutr. 1997 Mar;24(3):276-9. doi: 10.1097/00005176-199703000-00008. J Pediatr Gastroenterol Nutr. 1997. PMID: 9138172 Review.

9

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: labrune p. 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

10

In vivo 13C-NMR evaluation of glycogen content in a patient with glycogen storage disease.

Labrune P, Jehenson P, Syrota A, Odièvre M. Labrune P, et al. J Inherit Metab Dis. 1992;15(5):723-6. doi: 10.1007/BF01800013. J Inherit Metab Dis. 1992. PMID: 1434511

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