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Apolipoprotein E polymorphism and serum concentrations in patients with glycogen storage disease type Ia.
Published in:
Journal of Inherited Metabolic Disease, 2000, v. 23, n. 2, p. 107, doi. 10.1023/A:1005605513534
By:
- Trioche, P.;
- Francoual, J.;
- Capel, L.;
- Odièvre, M.;
- Lindenbaum, A.;
- Labrune, P.
Publication type:
Article
Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency.
Published in:
1999
By:
- Labrune, P.;
- Zittoun, J.;
- Duvaltier, I.;
- Trioche, P.;
- Marquet, J.;
- Niaudet, P.;
- Odièvre, M.;
- Odièvre, M
Publication type:
journal article
Molecular cytogenetic analysis of a Xp21.3-pter deletion in a family with normal and short stature.
Published in:
Clinical Genetics, 2002, v. 61, n. 2, p. 163, doi. 10.1034/j.1399-0004.2002.610214.x
By:
- Tachdjian, G;
- Perreaux, F;
- Aboura, A;
- Chevalier, P;
- Portnoi, M-F;
- Esteva, B;
- Trioche, P;
- Labrune, P
Publication type:
Article
Azathioprine-induced lung toxicity and efficacy of cyclosporin A in a young girl with type 2 autoimmune hepatitis.
Published in:
2000
By:
- Perreaux, Francis;
- Zenaty, Delphine;
- Capron, Frédérique;
- Trioche, Pascale;
- Odièvre, Michel;
- Labrune, Philippe;
- Perreaux, F;
- Zenaty, D;
- Capron, F;
- Trioche, P;
- Odièvre, M;
- Labrune, P
Publication type:
journal article
Hepatocellular adenomas in glycogen storage disease type I and III: a series of 43 patients and review of the literature.
Published in:
1997
By:
- Labrune, Philippe;
- Trioche, Pascale;
- Duvaltier, Isabelle;
- Chevalier, Paquita;
- Odièvre, Michel;
- Labrune, P;
- Trioche, P;
- Duvaltier, I;
- Chevalier, P;
- Odièvre, M
Publication type:
journal article
Allelic heterogeneity of glycogen storage disease type Ib in French patients: A study of 11 cases.
Published in:
Journal of Inherited Metabolic Disease, 2004, v. 27, n. 5, p. 621, doi. 10.1023/B:BOLI.0000042987.43395.c6
By:
- Trioche, P.;
- Petit, F.;
- Francoual, J.;
- Gajdos, V.;
- Capel, L.;
- Poüs, C.;
- Labrune, P.
Publication type:
Article

Found: 6

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

Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency.

Molecular cytogenetic analysis of a Xp21.3-pter deletion in a family with normal and short stature.

Azathioprine-induced lung toxicity and efficacy of cyclosporin A in a young girl with type 2 autoimmune hepatitis.

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

Allelic heterogeneity of glycogen storage disease type Ib in French patients: A study of 11 cases.