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S. Vicart · SciRah

Researcher profile · Semantic Scholar

S. Vicart

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S. Vicart — researcher profile on SciRah

h-index: 17
Works: 61
Citations: 1,185

Most-cited papers

Electromyography guides toward subgroups of mutations in muscle channelopathies
E. Fournier, M. Arzel, D. Sternberg, S. Vicart +5 more
2004Annals of Neurology302 citations
Semantic Scholar
Spectrum of HSPG2 (Perlecan) mutations in patients with Schwartz‐Jampel syndrome
M. Stum, C. Davoine, S. Vicart, L. Guillot-nöel +10 more
2006Human Mutation113 citations Open access
Semantic Scholar
Guidelines on clinical presentation and management of nondystrophic myotonias
Bas C. Stunnenberg, S. Lorusso, W. Arnold, R. Barohn +11 more
2020Muscle and Nerve89 citations Open access
Semantic Scholar
Human skeletal muscle sodium channelopathies
S. Vicart, D. Sternberg, B. Fontaine, G. Meola
2005Neurological Sciences89 citations
Semantic Scholar
Severe neonatal episodic laryngospasm due to de novo SCN4A mutations
L. Lion-Francois, C. Mignot, S. Vicart, V. Manel +8 more
2010Neurology79 citations
Semantic Scholar
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis
S. Vicart, D. Sternberg, E. Fournier, F. Ochsner +5 more
2004Neurology78 citations
Semantic Scholar
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients
J. P. Molenaar, J. Verhoeven, R. Rodenburg, E. Kamsteeg +27 more
2020Brain : a journal of neurology36 citations Open access
Semantic Scholar
Glucocorticoids may trigger attacks in several types of periodic paralysis.
M. Arzel‐hézode, S. McGoey, D. Sternberg, S. Vicart +2 more
2009Neuromuscular Disorders34 citations
Semantic Scholar
Homozygosity for dominant mutations increases severity of muscle channelopathies
M. Arzel‐hézode, D. Sternberg, N. Tabti, S. Vicart +4 more
2010Muscle and Nerve33 citations
Semantic Scholar
Efficacy and safety of mexiletine in non-dystrophic myotonias: A randomised, double-blind, placebo-controlled, cross-over study.
S. Vicart, J. Franques, F. Bouhour, A. Magot +10 more
2021Neuromuscular Disorders32 citations Open access
Semantic Scholar
Long-standing prion dementia manifesting as posterior cortical atrophy.
R. Depaz, S. Haïk, K. Peoc'h, D. Seilhean +9 more
2012Alzheimer Disease and Associated Disorders32 citations
Semantic Scholar
NEONATAL HYPOTONIA CAN BE A SODIUM CHANNELOPATHY: RECOGNITION OF A NEW PHENOTYPE
E. Matthews, A. Guet, M. Mayer, S. Vicart +4 more
2008Neurology31 citations Open access
Semantic Scholar
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia.
A. Furby, S. Vicart, J. Camdessanche, E. Fournier +7 more
2014Neuromuscular Disorders30 citations
Semantic Scholar
Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision Medicine
J. Desaphy, C. Altamura, S. Vicart, B. Fontaine
2020Journal of Neuromuscular Diseases29 citations Open access
Semantic Scholar
Perturbed Microbiota/Immune Homeostasis in Multiple Sclerosis
D. Sterlin, M. Larsen, J. Fadlallah, C. Parizot +13 more
2021Neurology: Neuroimmunology & Neuroinflammation26 citations Open access
Semantic Scholar
Hypokalemic periodic paralysis: A model for a clinical and research approach to a rare disorder
B. Fontaine, E. Fournier, D. Sternberg, S. Vicart +1 more
2007Neurotherapeutics23 citations Open access
Semantic Scholar
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes.
Sabrina Sacconi, Dina Simkin, Nicole Arrighi, F. Chapon +7 more
2009American Journal of Physiology - Cell Physiology22 citations
Semantic Scholar
Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralyses
Hugo Poulin, Pascal Gosselin-Badaroudine, S. Vicart, K. Habbout +6 more
2018Scientific Reports17 citations Open access
Semantic Scholar
A multicenter cross-sectional French study of the impact of COVID-19 on neuromuscular diseases
L. Pisella, S. Fernandes, G. Solé, T. Stojkovic +41 more
2021Orphanet Journal of Rare Diseases12 citations Open access
Semantic Scholar
Hypokalaemic periodic paralysis with a charge-retaining substitution in the voltage sensor
T. Kubota, Fen-Fen Wu, S. Vicart, Maki Nakaza +9 more
2020Brain Communications12 citations Open access
Semantic Scholar
[Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case].
A. Dervaux, S. Vicart, F. Lopes, M. Le Borgne
2001L'Encephale12 citations
Semantic Scholar
A204E mutation in Nav1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs
Y. Kokunai, C. Dalle, S. Vicart, D. Sternberg +6 more
2018Scientific Reports10 citations Open access
Semantic Scholar
Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort
E. Berling, Camille Verebi, N. Venturelli, S. Vassilopoulos +13 more
2023European Journal of Neurology7 citations Open access
Semantic Scholar
Phenotypical variability and atypical presentations in a French cohort of Andersen–Tawil syndrome
R. Villar-Quiles, D. Sternberg, G. Trédez, N. Romero +17 more
2022European Journal of Neurology7 citations
Semantic Scholar
[Nitric-oxide triggered neurological disorders in subjects with vitamin B12 deficiency].
F. C. Aubart, F. Sedel, S. Vicart, O. Lyon-Caen +1 more
2007Revue neurologique (Paris)7 citations
Semantic Scholar
E-Health & Innovation to Overcome Barriers in Neuromuscular Diseases. Report from the 1st eNMD Congress: Nice, France, March 22-23, 2019
Jonathan Pini, G. Siciliano, Pauline Lahaut, S. Braun +18 more
2021Journal of Neuromuscular Diseases6 citations Open access
Semantic Scholar
Psychiatric features of vCJD similar in France and UK
A. Dervaux, S. Vicart, F. Lopes, M. Le Borgne
2001British Journal of Psychiatry5 citations Open access
Semantic Scholar
Care Recommendations for the Investigation and Management of Children With Skeletal Muscle Channelopathies.
E. Matthews, Jacqueline A Palace, S. Ramdas, V. Sansone +3 more
2023Pediatric Neurology4 citations Open access
Semantic Scholar
Brody myopathy demonstrates a pseudo‐increment on repetitive nerve stimulation
M. Masingue, Marianne Arzel, D. Sternberg, T. Stojkovic +8 more
2020Muscle and Nerve4 citations
Semantic Scholar
Early radiological features of severe longitudinally extensive transverse myelitis over time.
S. Cattan, C. Papeix, D. Grabli, O. Casez +5 more
2019Journal of Neurological Sciences2 citations Open access
Semantic Scholar
Multiple cervical dissections after Rituximab.
T. Roux, S. Vicart, N. Shor, R. de Paz +3 more
2020Multiple Sclerosis and Related Disorders1 citations
Semantic Scholar
D.P.2.13 Neonatal hypotonia can be a sodium channelopathy
Emma L. Matthews, A. Guet, M. Mayer, S. Vicart +4 more
20081 citations
Semantic Scholar
Neonatal hypotonia can be a sodium channelopathy
E. Matthews, A. Guet, M. Mayer, S. Vicart +4 more
20081 citations
Semantic Scholar
Functional Immuno-metagenomics Seizes the Alteration of Microbiota-Immune Interactions at the Early Onset of Multiple Sclerosis
Nthuku Simeon, Pons Nicolas, Parizot Christophe, L. Martin +7 more
2026bioRxiv0 citations
Semantic Scholar
4.68P Hypokalemic periodic paralysis meets panhypopituitarism: a novel phenotype
P. Panos-Basterra, Oceana Vieira Pinto-Delaville, G. Taieb, J. Noury +4 more
2026Neuromuscular Disorders0 citations
Semantic Scholar
Genome sequencing improves diagnostic outcomes over panel and exome sequencings in myopathies: findings from the French PFMG2025 initiative
Camille Verebi, A. Maino, C. Métay, J. Nectoux +115 more
2026Genome Medicine0 citations Open access
Semantic Scholar
Antibody-mediated immune surveillance as an organizing axis of gut microbiota structure
Simeon Nthuku, D. Sterlin, N. Pons, C. Parizot +8 more
2026Microbiome0 citations Open access
Semantic Scholar
The RaDiCo information system for rare disease cohorts
Paul Landais, Sonia Gueguen, A. Clément, S. Amselem +18 more
2025Orphanet Journal of Rare Diseases0 citations Open access
Semantic Scholar
Development of the Clinical Myotonia Rating Scale and a Mexiletine Prescribing and Monitoring Algorithm for Patients with Non-Dystrophic Myotonia
S. Vicart, E. Roberts
2023EMJ Neurology0 citations Open access
Semantic Scholar
CHANNELOPATHIES AND RELATED DISORDERS
R. Quiles, G. Trédez, D. Sternberg, N. Romero +11 more
2021Neuromuscular Disorders0 citations
Semantic Scholar
CHANNELOPATHIES AND RELATED DISORDERS
S. Vicart, J. Franques, F. Bouhour, A. Magot +10 more
2021Neuromuscular Disorders0 citations
Semantic Scholar
P.100Pseudo-increment at repetitive nerve stimulation (Arzel's sign): a new tool for Brody myopathy diagnosis
M. Masingue, Marianne Arzel, D. Sternberg, T. Stojkovic +7 more
2019Neuromuscular Disorders0 citations
Semantic Scholar
Biophysical Characterization of Two NaV1.4 Mutations Making a Clinical Overlap between the Myotonia-Hyperkalemic and Hypokalemic Periodic Paralysis Clusters of Disorders
M. Chahine, Hugo Poulin, Pascal Gosselin-Badaroudine, S. Vicart +6 more
20180 citations Open access
Semantic Scholar
Hypokalemic Periodic Paralysis Cases with Substitutions from Arginine to Lysine in the Voltage Sensor
Maki Nakaza, T. Kubota, S. Vicart, D. Watanabe +7 more
20180 citations Open access
Semantic Scholar
Spinal Angiogram: A Treacherous Criterion Standard…
F. Clarençon, E. Shotar, A. Boch, C. Rolla-Bigliani +5 more
2018American Journal of Neuroradiology0 citations Open access
Semantic Scholar
P.227 - The Brody disease cohort study: clarification of the phenotype
J. P. Molenaar, J. Verhoeven, N. Voermans, J. Mathieu +13 more
20170 citations
Semantic Scholar
A case of periodic paralysis with hypo and hyperkalemic characteristics
Yosuke Kokunai, S. Vicart, C. Dalle, D. Sternberg +2 more
20170 citations
Semantic Scholar
Biophysical Characterization of Two Nav1.4 Mutations Identified in Patients with Cold-Induced Myotonia and Periodic Paralysis
Hugo Poulin, Pascal Gosselin-Badaroudine, K. Habbout, S. Vicart +5 more
20160 citations Open access
Semantic Scholar
Table 10. [KCNJ18 Pathogenic Variants Discussed in This GeneReview].
S. Vicart, D. Sternberg, M. Arzel‐hézode, J. Franques +6 more
20140 citations
Semantic Scholar
Table 6. [Identifying the Cause of Secondary Hypokalemia].
S. Vicart, D. Sternberg, M. Arzel‐hézode, J. Franques +6 more
20140 citations
Semantic Scholar

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