Vaxillaire M - Search Results

1

Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations.

Gonsorcikova L, Vaxillaire M, Pruhova S, Dechaume A, Dusatkova P, Cinek O, Pedersen O, Froguel P, Hansen T, Lebl J. Gonsorcikova L, et al. Among authors: vaxillaire m. Pediatr Diabetes. 2011 May;12(3 Pt 2):266-9. doi: 10.1111/j.1399-5448.2010.00719.x. Epub 2011 Jan 9. Pediatr Diabetes. 2011. PMID: 21214702

2

Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM.

Lesage S, Hani EH, Philippi A, Vaxillaire M, Hager J, Passa P, Demenais F, Froguel P, Vionnet N. Lesage S, et al. Among authors: vaxillaire m. Diabetes. 1995 Oct;44(10):1243-7. doi: 10.2337/diab.44.10.1243. Diabetes. 1995. PMID: 7556965

3

Isolation of the human LIM/homeodomain gene islet-1 and identification of a simple sequence repeat polymorphism [corrected].

Tanizawa Y, Riggs AC, Dagogo-Jack S, Vaxillaire M, Froguel P, Liu L, Donis-Keller H, Permutt MA. Tanizawa Y, et al. Among authors: vaxillaire m. Diabetes. 1994 Jul;43(7):935-41. doi: 10.2337/diab.43.7.935. Diabetes. 1994. PMID: 7912209

4

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.

Froguel P, Zouali H, Vionnet N, Velho G, Vaxillaire M, Sun F, Lesage S, Stoffel M, Takeda J, Passa P, et al. Froguel P, et al. Among authors: vaxillaire m. N Engl J Med. 1993 Mar 11;328(10):697-702. doi: 10.1056/NEJM199303113281005. N Engl J Med. 1993. PMID: 8433729 Free article.

5

Identification of trinucleotide repeat-containing genes in human pancreatic islets.

Aoki M, Koranyi L, Riggs AC, Wasson J, Chiu KC, Vaxillaire M, Froguel P, Gough S, Liu L, Donis-Keller H, et al. Aoki M, et al. Among authors: vaxillaire m. Diabetes. 1996 Feb;45(2):157-64. doi: 10.2337/diab.45.2.157. Diabetes. 1996. PMID: 8549859

6

Diabetes complications in NIDDM kindreds linked to the MODY3 locus on chromosome 12q.

Velho G, Vaxillaire M, Boccio V, Charpentier G, Froguel P. Velho G, et al. Among authors: vaxillaire m. Diabetes Care. 1996 Sep;19(9):915-9. doi: 10.2337/diacare.19.9.915. Diabetes Care. 1996. PMID: 8875082

7

Diagnostic heterogeneity of diabetes in lean young adults: classification based on immunological and genetic parameters.

Dussoix P, Vaxillaire M, Iynedjian PB, Tiercy JM, Ruiz J, Spinas GA, Berger W, Zahnd G, Froguel P, Philippe J. Dussoix P, et al. Among authors: vaxillaire m. Diabetes. 1997 Apr;46(4):622-31. doi: 10.2337/diab.46.4.622. Diabetes. 1997. PMID: 9075802

8

Novel MODY3 mutations in the hepatocyte nuclear factor-1alpha gene: evidence for a hyperexcitability of pancreatic beta-cells to intravenous secretagogues in a glucose-tolerant carrier of a P447L mutation.

Hansen T, Eiberg H, Rouard M, Vaxillaire M, Møller AM, Rasmussen SK, Fridberg M, Urhammer SA, Holst JJ, Almind K, Echwald SM, Hansen L, Bell GI, Pedersen O. Hansen T, et al. Among authors: vaxillaire m. Diabetes. 1997 Apr;46(4):726-30. doi: 10.2337/diab.46.4.726. Diabetes. 1997. PMID: 9075819

9

Glucose utilization and production in patients with maturity-onset diabetes of the young caused by a mutation of the hepatocyte nuclear factor-1alpha gene.

Surmely JF, Guenat E, Philippe J, Dussoix P, Schneiter P, Temler E, Vaxillaire M, Froguel P, Jéquier E, Tappy L. Surmely JF, et al. Among authors: vaxillaire m. Diabetes. 1998 Sep;47(9):1459-63. doi: 10.2337/diabetes.47.9.1459. Diabetes. 1998. PMID: 9726235

10

Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians.

Abderrahmani A, Chèvre JC, Otabe S, Chikri M, Hani EH, Vaxillaire M, Hinokio Y, Horikawa Y, Bell GI, Froguel P. Abderrahmani A, et al. Among authors: vaxillaire m. Diabetes. 2000 Feb;49(2):306-8. doi: 10.2337/diabetes.49.2.306. Diabetes. 2000. PMID: 10868949

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