Labrune P - Search Results

1

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.

2

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

3

Fetal type IV glycogen storage disease: clinical, enzymatic, and genetic data of a pure muscular form with variable and early antenatal manifestations in the same family.

L'herminé-Coulomb A, Beuzen F, Bouvier R, Rolland MO, Froissart R, Menez F, Audibert F, Labrune P. L'herminé-Coulomb A, et al. Among authors: labrune p. Am J Med Genet A. 2005 Dec 1;139A(2):118-22. doi: 10.1002/ajmg.a.30945. Am J Med Genet A. 2005. PMID: 16278887

4

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.

5

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

6

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

7

Progressive neuronal degeneration of childhood: prenatal diagnosis by MRI.

de Laveaucoupet J, Roffi F, Audibert F, Guis F, Lacroix C, Villeneuve N, Landrieu P, Labrune P. de Laveaucoupet J, et al. Among authors: labrune p. Prenat Diagn. 2005 Apr;25(4):307-10. doi: 10.1002/pd.1128. Prenat Diagn. 2005. PMID: 15852481

8

[Natural history of hepatic glycogen storage diseases].

Labrune P, Eberschweiler PT, Boudjemline AM, Hubert-Buron A, Petit F, Gajdos V. Labrune P, et al. Presse Med. 2008 Jul-Aug;37(7-8):1172-7. doi: 10.1016/j.lpm.2007.09.023. Epub 2008 Feb 29. Presse Med. 2008. PMID: 18313893 Review. French.

9

Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15.

L'Herminé AC, Aboura A, Brisset S, Cuisset L, Castaigne V, Labrune P, Frydman R, Tachdjian G. L'Herminé AC, et al. Among authors: labrune p. Prenat Diagn. 2003 Nov;23(11):938-43. doi: 10.1002/pd.732. Prenat Diagn. 2003. PMID: 14634983

10

Antenatal thrombocytopenia in three patients with TAR (thrombocytopenia with absent radii) syndrome.

Labrune P, Pons JC, Khalil M, Mirlesse V, Imbert MC, Odièvre M, Daffos F, Tchernia G, Frydman R. Labrune P, et al. Prenat Diagn. 1993 Jun;13(6):463-6. doi: 10.1002/pd.1970130607. Prenat Diagn. 1993. PMID: 8372072

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

246 results

Search Page

Filters