Vicart S - Search Results

1

Guidelines on clinical presentation and management of nondystrophic myotonias.

Stunnenberg BC, LoRusso S, Arnold WD, Barohn RJ, Cannon SC, Fontaine B, Griggs RC, Hanna MG, Matthews E, Meola G, Sansone VA, Trivedi JR, van Engelen BGM, Vicart S, Statland JM. Stunnenberg BC, et al. Among authors: vicart s. Muscle Nerve. 2020 Oct;62(4):430-444. doi: 10.1002/mus.26887. Epub 2020 May 27. Muscle Nerve. 2020. PMID: 32270509 Free PMC article. Review.

2

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.

3

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

4

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.

5

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.

6

[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.

7

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.

8

Glucocorticoids may trigger attacks in several types of periodic paralysis.

Arzel-Hézode M, McGoey S, Sternberg D, Vicart S, Eymard B, Fontaine B. Arzel-Hézode M, et al. Among authors: vicart s. Neuromuscul Disord. 2009 Mar;19(3):217-9. doi: 10.1016/j.nmd.2008.12.008. Epub 2009 Feb 7. Neuromuscul Disord. 2009. PMID: 19201608

9

Homozygosity for dominant mutations increases severity of muscle channelopathies.

Arzel-Hézode M, Sternberg D, Tabti N, Vicart S, Goizet C, Eymard B, Fontaine B, Fournier E. Arzel-Hézode M, et al. Among authors: vicart s. Muscle Nerve. 2010 Apr;41(4):470-7. doi: 10.1002/mus.21520. Muscle Nerve. 2010. PMID: 19882638

10

Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorder.

Lion-Francois L, Mignot C, Vicart S, Manel V, Sternberg D, Landrieu P, Lesca G, Broussolle E, Billette de Villemeur T, Napuri S, des Portes V, Fontaine B. Lion-Francois L, et al. Among authors: vicart s. Neurology. 2010 Aug 17;75(7):641-5. doi: 10.1212/WNL.0b013e3181ed9e96. Neurology. 2010. PMID: 20713951

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