Vialettes B - Search Results

1

Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome.

Cano A, Rouzier C, Monnot S, Chabrol B, Conrath J, Lecomte P, Delobel B, Boileau P, Valero R, Procaccio V, Paquis-Flucklinger V; French Group of Wolfram Syndrome; Vialettes B. Cano A, et al. Among authors: vialettes b. Am J Med Genet A. 2007 Jul 15;143A(14):1605-12. doi: 10.1002/ajmg.a.31809. Am J Med Genet A. 2007. PMID: 17568405

2

Microvascular diabetes complications in Wolfram syndrome (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness [DIDMOAD]): an age- and duration-matched comparison with common type 1 diabetes.

Cano A, Molines L, Valéro R, Simonin G, Paquis-Flucklinger V, Vialettes B; French Group of Wolfram Syndrome. Cano A, et al. Among authors: vialettes b. Diabetes Care. 2007 Sep;30(9):2327-30. doi: 10.2337/dc07-0380. Epub 2007 May 29. Diabetes Care. 2007. PMID: 17536072

3

Neurologic features and genotype-phenotype correlation in Wolfram syndrome.

Chaussenot A, Bannwarth S, Rouzier C, Vialettes B, Mkadem SA, Chabrol B, Cano A, Labauge P, Paquis-Flucklinger V. Chaussenot A, et al. Among authors: vialettes b. Ann Neurol. 2011 Mar;69(3):501-8. doi: 10.1002/ana.22160. Epub 2010 Dec 28. Ann Neurol. 2011. PMID: 21446023

4

Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene.

Giuliano F, Bannwarth S, Monnot S, Cano A, Chabrol B, Vialettes B, Delobel B, Paquis-Flucklinger V; French Group of WS. Giuliano F, et al. Among authors: vialettes b. Hum Mutat. 2005 Jan;25(1):99-100. doi: 10.1002/humu.9300. Hum Mutat. 2005. PMID: 15605410

5

Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in the WFS1 gene.

Valéro R, Bannwarth S, Roman S, Paquis-Flucklinger V, Vialettes B. Valéro R, et al. Among authors: vialettes b. Diabet Med. 2008 Jun;25(6):657-61. doi: 10.1111/j.1464-5491.2008.02448.x. Diabet Med. 2008. PMID: 18544103

6

Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations.

Decoux-Poullot AG, Bannwarth S, Procaccio V, Lebre AS, Jardel C, Vialettes B, Paquis-Flucklinger V, Chevalier N. Decoux-Poullot AG, et al. Among authors: vialettes b. Ann Endocrinol (Paris). 2020 Jun;81(2-3):68-77. doi: 10.1016/j.ando.2020.04.007. Epub 2020 Apr 28. Ann Endocrinol (Paris). 2020. PMID: 32409007

7

Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders.

Chaussenot A, Rouzier C, Quere M, Plutino M, Ait-El-Mkadem S, Bannwarth S, Barth M, Dollfus H, Charles P, Nicolino M, Chabrol B, Vialettes B, Paquis-Flucklinger V. Chaussenot A, et al. Among authors: vialettes b. Clin Genet. 2015 May;87(5):430-9. doi: 10.1111/cge.12437. Epub 2014 Aug 6. Clin Genet. 2015. PMID: 24890733

8

Clinical aspects of mitochondrial diabetes.

Vialettes B, Paquis-Flucklinger V, Bendahan D. Vialettes B, et al. Diabetes Metab. 1997 Mar;23 Suppl 2:52-6. Diabetes Metab. 1997. PMID: 9105784 Review.

9

[Monogenic diabetes: a useful dimension for diabetology practice].

Valéro R, Béliard S, Paquis-Fluckinger V, Vialettes B. Valéro R, et al. Among authors: vialettes b. Ann Endocrinol (Paris). 2005 Jun;66(3):279-83. doi: 10.1016/s0003-4266(05)81762-7. Ann Endocrinol (Paris). 2005. PMID: 15988391 Review. French.

10

Brain anomalies in maternally inherited diabetes and deafness syndrome.

Fromont I, Nicoli F, Valéro R, Felician O, Lebail B, Lefur Y, Mancini J, Paquis-Flucklinger V, Cozzone PJ, Vialettes B. Fromont I, et al. Among authors: vialettes b. J Neurol. 2009 Oct;256(10):1696-704. doi: 10.1007/s00415-009-5185-4. Epub 2009 Jun 18. J Neurol. 2009. PMID: 19536585

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