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, J.-B., Nadaj-Pakleza, A., Tard, C., Sacconi, S.
Published in Revue neurologique (28.05.2024)
Published in Revue neurologique (28.05.2024)
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Journal Article
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
Published in Neurology (17.08.2010)
Published in Neurology (17.08.2010)
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Journal Article
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia
Furby, A, Vicart, S, Camdessanché, J.P, Fournier, E, Chabrier, S, Lagrue, E, Paricio, C, Blondy, P, Touraine, R, Sternberg, D, Fontaine, B
Published in Neuromuscular disorders : NMD (01.11.2014)
Published in Neuromuscular disorders : NMD (01.11.2014)
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Journal Article
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
Published in Neurology (14.12.2004)
Published in Neurology (14.12.2004)
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Journal Article
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, M G
Published in Neurology (18.11.2008)
Published in Neurology (18.11.2008)
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Journal Article
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes
Sacconi, S, Simkin, D, Arrighi, N, Chapon, F, Larroque, M. M, Vicart, S, Sternberg, D, Fontaine, B, Barhanin, J, Desnuelle, C, Bendahhou, S
Published in American Journal of Physiology: Cell Physiology (01.10.2009)
Published in American Journal of Physiology: Cell Physiology (01.10.2009)
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Journal Article
D.P.2.13 Neonatal hypotonia can be a sodium channelopathy
Matthews, E, Guet, A, Mayer, M, Vicart, S, Pemble, S, Sternberg, D, Fontaine, B, Hanna, M.G
Published in Neuromuscular disorders : NMD (01.10.2008)
Published in Neuromuscular disorders : NMD (01.10.2008)
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Journal Article
Nitric-oxide triggered neurological disorders in subjects with vitamin B12 deficiency
Cohen Aubart, F, Sedel, F, Vicart, S, Lyon-Caen, O, Fontaine, B
Published in Revue neurologique (01.03.2007)
Published in Revue neurologique (01.03.2007)
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Journal Article
P387 Initiation and follow-up of mexiletine treatment in adult myotonic dystrophy patients: an expert opinion
Wahbi, K., Bassez, G., Duchateau, J., Salort-Campana, E., Vicart, S., Labombarda, F., Sellal, J., Deharo, J.
Published in Neuromuscular disorders : NMD (01.10.2023)
Published in Neuromuscular disorders : NMD (01.10.2023)
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Journal Article
P395 Recommendations of an expert group for cardiac assessment of non-dystrophic myotonic adult patients treated with mexiletine
Vicart, S., Wahbi, K., Duchateau, J., Sellal, J., Deharo, J., Bassez, G., Salort-Campana, E., Labombarda, F.
Published in Neuromuscular disorders : NMD (01.10.2023)
Published in Neuromuscular disorders : NMD (01.10.2023)
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Journal Article
Psychiatric features of vCJD similar in France and UK
Dervaux, A, Vicart, S, Lopes, F, Le Borgne, M H
Published in British journal of psychiatry (01.03.2001)
Published in British journal of psychiatry (01.03.2001)
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Journal Article
A case of periodic paralysis with hypo and hyperkalemic characteristics
Kokunai, Y., Vicart, S., Dalle, C., Sternberg, D., Fontaine, B., Nicole, S.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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Journal Article
CHANNELOPATHIES AND RELATED DISORDERS: EP.221 Diagnostic delay and atypical phenotypes in a French cohort of Andersen-Tawil syndrome
Quiles, R. Villar, Tredez, G., Sternberg, D., Romero, N., Evangelista, T., Laforêt, P., Cintas, P., Sole, G., Sacconi, S., Bendahhou, S., Arzel-Hezode, M., Fournier, E., Fontaine, B., Stojkovic, T., Vicart, S.
Published in Neuromuscular disorders : NMD (01.10.2021)
Published in Neuromuscular disorders : NMD (01.10.2021)
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Journal Article
CHANNELOPATHIES AND RELATED DISORDERS
Vicart, S., Franques, J., Bouhour, F., Magot, A., Péréon, Y., Sacconi, S., Nadaj-Pakleza, A., Behin, A., Zahr, N., Hezode, M., Fournier, E., Payan, C., Lacomblez, L., Fontaine, B.
Published in Neuromuscular disorders : NMD (01.10.2021)
Published in Neuromuscular disorders : NMD (01.10.2021)
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Journal Article
CHANNELOPATHIES AND RELATED DISORDERS: EP.228 Efficacy and safety of mexiletine in non-dystrophic myotonias: a randomized, double-blind, placebo-controlled, cross-over study
Vicart, S., Franques, J., Bouhour, F., Magot, A., Péréon, Y., Sacconi, S., Nadaj-Pakleza, A., Behin, A., Zahr, N., Hezode, M., Fournier, E., Payan, C., Lacomblez, L., Fontaine, B.
Published in Neuromuscular disorders : NMD (01.10.2021)
Published in Neuromuscular disorders : NMD (01.10.2021)
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Journal Article
CHANNELOPATHIES AND RELATED DISORDERS
Quiles, R. Villar, Tredez, G., Sternberg, D., Romero, N., Evangelista, T., Laforêt, P., Cintas, P., Sole, G., Sacconi, S., Bendahhou, S., Arzel-Hezode, M., Fournier, E., Fontaine, B., Stojkovic, T., Vicart, S.
Published in Neuromuscular disorders : NMD (01.10.2021)
Published in Neuromuscular disorders : NMD (01.10.2021)
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Journal Article
P.100Pseudo-increment at repetitive nerve stimulation (Arzel's sign): a new tool for Brody myopathy diagnosis
Masingue, M., Arzel, M., Sternberg, D., Stojkovic, T., Behin, A., Bassez, G., Vicart, S., Péréon, Y., Kuntzer, T., Eymard, B., Fournier, E.
Published in Neuromuscular disorders : NMD (01.10.2019)
Published in Neuromuscular disorders : NMD (01.10.2019)
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Journal Article
Electromyography guides toward subgroups of mutations in muscle channelopathies
Fournier, Emmanuel, Arzel, Marianne, Sternberg, Damien, Vicart, Savine, Laforet, Pascal, Eymard, Bruno, Willer, Jean-Claude, Tabti, Nacira, Fontaine, Bertrand
Published in Annals of neurology (01.11.2004)
Published in Annals of neurology (01.11.2004)
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Journal Article
Troubles neurologiques par carence en vitamine B12 déclenchés par le protoxyde d’azote
Cohen Aubart, F., Sedel, F., Vicart, S., Lyon-Caen, O., Fontaine, B.
Published in Revue neurologique (01.03.2007)
Published in Revue neurologique (01.03.2007)
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Journal Article