S. Vicart

发表

Efficacy and safety of mexiletine in non-dystrophic myotonias: A randomised, double-blind, placebo-controlled, cross-over study

Y. Péréon, N. Zahr, A. Béhin, 2021, Neuromuscular Disorders.

Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia

R. Touraine, B. Fontaine, S. Vicart, 2014, Neuromuscular Disorders.

Electromyography guides toward subgroups of mutations in muscle channelopathies

J. Willer, P. Laforêt, B. Eymard, 2004, Annals of neurology.

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

H. Kayserili, B. Fontaine, C. Davoine, 2006, Human mutation.

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

P. Laforêt, B. Eymard, T. Kuntzer, 2004, Neurology.

Psychiatric features of vCJD similar in France and UK

S. Vicart, A. Dervaux, M. Borgne, 2001, British Journal of Psychiatry.

Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision Medicine

B. Fontaine, S. Vicart, J. Desaphy, 2020, Journal of neuromuscular diseases.

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

B. Fontaine, S. Vicart, E. Fournier, 2007, Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics.

Human skeletal muscle sodium channelopathies

G. Meola, B. Fontaine, S. Vicart, 2005, Neurological Sciences.

Phenotypical variability and atypical presentations in a French cohort of Andersen–Tawil syndrome

N. Romero, S. Bendahhou, P. Laforêt, 2022, European journal of neurology.

Long-standing prion dementia manifesting as posterior cortical atrophy.

C. Fallet-Bianco, D. Grabli, M. Sarazin, 2012, Alzheimer disease and associated disorders.

Spinal Angiogram: A Treacherous Criterion Standard…

D. Grabli, N. Sourour, J. Chiras, 2018, American Journal of Neuroradiology.

A204E mutation in Nav1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs

S. Bendahhou, B. Fontaine, S. Vicart, 2018, Scientific Reports.

Hypokalaemic periodic paralysis with a charge-retaining substitution in the voltage sensor

S. Cannon, N. Kokubun, B. Fontaine, 2020, Brain communications.

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

F. Sedel, B. Fontaine, S. Vicart, 2007, Revue neurologique (Paris).

Guidelines on clinical presentation and management of nondystrophic myotonias

S. Cannon, R. Griggs, G. Meola, 2020, Muscle & nerve.

Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients

R. Rodenburg, G. Bassez, B. V. van Engelen, 2020, Brain : a journal of neurology.

NEONATAL HYPOTONIA CAN BE A SODIUM CHANNELOPATHY: RECOGNITION OF A NEW PHENOTYPE

M. Hanna, B. Fontaine, S. Vicart, 2008, Neurology.

[Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case].

S. Vicart, M. Le Borgne, A. Dervaux, 2001, L'Encephale.

Perturbed Microbiota/Immune Homeostasis in Multiple Sclerosis

P. Lepage, C. Juste, S. Vicart, 2021, Neurology: Neuroimmunology & Neuroinflammation.

Glucocorticoids may trigger attacks in several types of periodic paralysis

B. Eymard, B. Fontaine, S. Vicart, 2009, Neuromuscular Disorders.

Hypokalemic Periodic Paralysis

P. Lory, S. Bendahhou, B. Hainque, 2014 .

Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralyses

S. Bendahhou, S. Vicart, B. Fontaine, 2018, Scientific Reports.

Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes.

F. Chapon, S. Bendahhou, M. Larroque, 2009, American journal of physiology. Cell physiology.

Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralyses

S. Bendahhou, B. Fontaine, S. Vicart, 2018, Scientific Reports.

Homozygosity for dominant mutations increases severity of muscle channelopathies

B. Eymard, B. Fontaine, C. Goizet, 2010, Muscle & nerve.

Brody myopathy demonstrates a pseudo‐increment on repetitive nerve stimulation

G. Bassez, Y. Péréon, B. Eymard, 2020, Muscle & nerve.

Care recommendations for the investigation and management of children with skeletal muscle channelopathies

Jacqueline A Palace, M. Tristani-Firouzi, S. Vicart, 2023, Pediatric Neurology.

E-Health & Innovation to Overcome Barriers in Neuromuscular Diseases. Report from the 1st eNMD Congress: Nice, France, March 22-23, 2019

L. Servais, G. Siciliano, H. Lochmüller, 2021, Journal of neuromuscular diseases.

myotubesin skeletal muscle are revealed in human Mechanisms underlying Andersen's syndrome

Claude Desnuelle, Bertrand Fontaine, Savine Vicart, 2011 .

Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort

R. Carlier, F. Leturcq, P. Laforêt, 2023, European journal of neurology.

Early radiological features of severe longitudinally extensive transverse myelitis over time

D. Grabli, C. Louapre, S. Vicart, 2019, Journal of the Neurological Sciences.