Vicart S - Search Results

1

A204E mutation in Na_v1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs.

Kokunai Y, Dalle C, Vicart S, Sternberg D, Pouliot V, Bendahhou S, Fournier E, Chahine M, Fontaine B, Nicole S. Kokunai Y, et al. Among authors: vicart s. Sci Rep. 2018 Nov 12;8(1):16681. doi: 10.1038/s41598-018-34750-8. Sci Rep. 2018. PMID: 30420713 Free PMC article.

2

Expert opinion on mexiletine treatment in adult patients with myotonic dystrophy.

Wahbi K, Bassez G, Duchateau J, Salort-Campana E, Vicart S, Desaphy JF, Labombarda F, Sellal JM, Deharo JC. Wahbi K, et al. Among authors: vicart s. Arch Cardiovasc Dis. 2024 Jun-Jul;117(6-7):450-456. doi: 10.1016/j.acvd.2024.03.001. Epub 2024 Apr 15. Arch Cardiovasc Dis. 2024. PMID: 38677940 Free article. Review.

3

Self-reported outcomes and quality of life of patients with non-dystrophic myotonia: The French IMPACT 2022 survey.

Vicart S, Péréon Y, Ghorab K, Pegat A, Dufresne R, Zozulya-Weidenfeller A, Noury JB, Nadaj-Pakleza A, Tard C, Sacconi S. Vicart S, et al. Rev Neurol (Paris). 2024 Oct;180(8):791-797. doi: 10.1016/j.neurol.2024.04.007. Epub 2024 May 28. Rev Neurol (Paris). 2024. PMID: 38811249 Free article.

4

Electromyography guides toward subgroups of mutations in muscle channelopathies.

Fournier E, Arzel M, Sternberg D, Vicart S, Laforet P, Eymard B, Willer JC, Tabti N, Fontaine B. Fournier E, et al. Among authors: vicart s. Ann Neurol. 2004 Nov;56(5):650-61. doi: 10.1002/ana.20241. Ann Neurol. 2004. PMID: 15389891 Clinical Trial.

5

New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis.

Vicart S, Sternberg D, Fournier E, Ochsner F, Laforet P, Kuntzer T, Eymard B, Hainque B, Fontaine B. Vicart S, et al. Neurology. 2004 Dec 14;63(11):2120-7. doi: 10.1212/01.wnl.0000145768.09934.ec. Neurology. 2004. PMID: 15596759

6

Human skeletal muscle sodium channelopathies.

Vicart S, Sternberg D, Fontaine B, Meola G. Vicart S, et al. Neurol Sci. 2005 Oct;26(4):194-202. doi: 10.1007/s10072-005-0461-x. Neurol Sci. 2005. PMID: 16193245 Review.

7

Spectrum of HSPG2 (Perlecan) mutations in patients with Schwartz-Jampel syndrome.

Stum M, Davoine CS, Vicart S, Guillot-Noël L, Topaloglu H, Carod-Artal FJ, Kayserili H, Hentati F, Merlini L, Urtizberea JA, Hammouda el-H, Quan PC, Fontaine B, Nicole S. Stum M, et al. Among authors: vicart s. Hum Mutat. 2006 Nov;27(11):1082-91. doi: 10.1002/humu.20388. Hum Mutat. 2006. PMID: 16927315

8

Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder.

Fontaine B, Fournier E, Sternberg D, Vicart S, Tabti N. Fontaine B, et al. Among authors: vicart s. Neurotherapeutics. 2007 Apr;4(2):225-32. doi: 10.1016/j.nurt.2007.01.002. Neurotherapeutics. 2007. PMID: 17395132 Free article. Review.

9

[Nitric-oxide triggered neurological disorders in subjects with vitamin B12 deficiency].

Cohen Aubart F, Sedel F, Vicart S, Lyon-Caen O, Fontaine B. Cohen Aubart F, et al. Among authors: vicart s. Rev Neurol (Paris). 2007 Mar;163(3):362-4. doi: 10.1016/s0035-3787(07)90409-9. Rev Neurol (Paris). 2007. PMID: 17404524 French.

10

Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotype.

Matthews E, Guet A, Mayer M, Vicart S, Pemble S, Sternberg D, Fontaine B, Hanna MG. Matthews E, et al. Among authors: vicart s. Neurology. 2008 Nov 18;71(21):1740-2. doi: 10.1212/01.wnl.0000335269.21550.0e. Neurology. 2008. PMID: 19015492 Free PMC article. No abstract available.

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