Labrune P - Search Results

1

Antley-Bixler syndrome. Description of two new cases and a review of the literature.

Bottero L, Cinalli G, Labrune P, Lajeunie E, Renier D. Bottero L, et al. Among authors: labrune p. Childs Nerv Syst. 1997 May;13(5):275-80; discussion 281. doi: 10.1007/s003810050082. Childs Nerv Syst. 1997. PMID: 9224917 Review.

2

[Antley-Bixler syndrome. Description of two new cases and review of the literature. Prognostic and therapeutic aspects].

Bottero L, Cinalli G, Labrune P, Lajeunie E, Marchac D, Renier D. Bottero L, et al. Among authors: labrune p. Ann Chir Plast Esthet. 1997 Feb;42(1):48-55. Ann Chir Plast Esthet. 1997. PMID: 9768136 Review. French.

3

CHARGE syndrome: report of 47 cases and review.

Tellier AL, Cormier-Daire V, Abadie V, Amiel J, Sigaudy S, Bonnet D, de Lonlay-Debeney P, Morrisseau-Durand MP, Hubert P, Michel JL, Jan D, Dollfus H, Baumann C, Labrune P, Lacombe D, Philip N, LeMerrer M, Briard ML, Munnich A, Lyonnet S. Tellier AL, et al. Among authors: labrune p. Am J Med Genet. 1998 Apr 13;76(5):402-9. doi: 10.1002/(sici)1096-8628(19980413)76:5<402::aid-ajmg7>3.0.co;2-o. Am J Med Genet. 1998. PMID: 9556299 Review.

4

Three new cases of the Schinzel-Giedion syndrome and review of the literature.

Labrune P, Lyonnet S, Zupan V, Imbert MC, Goutieres F, Hubert P, Le Merrer M. Labrune P, et al. Am J Med Genet. 1994 Mar 1;50(1):90-3. doi: 10.1002/ajmg.1320500120. Am J Med Genet. 1994. PMID: 8160760 Review.

5

Severe brain and limb defects with possible autosomal recessive inheritance: a series of six cases and review of the literature.

Labrune P, Trioche P, Fallet-Bianco C, Roume J, Narcy F, Le Merrer M. Labrune P, et al. Am J Med Genet. 1997 Dec 12;73(2):144-9. Am J Med Genet. 1997. PMID: 9409864 Review.

6

Congenital hepatic fibrosis, cystic kidneys, mental retardation, and facial dysmorphy: a new report of an autosomal recessive syndrome.

Labrune P, Lange JC, Bedossa P, Chaussain JL, Odievre M. Labrune P, et al. J Pediatr Gastroenterol Nutr. 1990 May;10(4):540-3. doi: 10.1097/00005176-199005000-00019. J Pediatr Gastroenterol Nutr. 1990. PMID: 2193138

7

Abdominal pain and ketonuria in an 11-year-old girl five months after abdominal trauma.

Gajdos V, Perreaux F, Brivet F, Vons C, Labrune P. Gajdos V, et al. Among authors: labrune p. J Pediatr Surg. 2002 Sep;37(9):1361-2. doi: 10.1053/jpsu.2002.35015. J Pediatr Surg. 2002. PMID: 12194135

8

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

9

Sweet syndrome as the presenting manifestation of chronic granulomatous disease in an infant.

Sedel D, Huguet P, Lebbe C, Donadieu J, Odièvre M, Labrune P. Sedel D, et al. Among authors: labrune p. Pediatr Dermatol. 1994 Sep;11(3):237-40. doi: 10.1111/j.1525-1470.1994.tb00593.x. Pediatr Dermatol. 1994. PMID: 7971558

10

Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 cases.

Labrune P, Myara A, Hadchouel M, Ronchi F, Bernard O, Trivin F, Chowdhury NR, Chowdhury JR, Munnich A, Odièvre M. Labrune P, et al. Hum Genet. 1994 Dec;94(6):693-7. doi: 10.1007/BF00206965. Hum Genet. 1994. PMID: 7989045

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