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Savine Vicart

Showing results (1-10 of 25) with videos related to

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Journal of Neuromuscular Diseases|December 16, 2020
Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision MedicineJean-François Desaphy, Concetta Altamura, Savine Vicart, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 31, 2007
Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorderBertrand Fontaine, Emmanuel Fournier, Damien Sternberg, et al.
Neuromuscular Disorders : NMD|February 10, 2009
Glucocorticoids may trigger attacks in several types of periodic paralysisMarianne Arzel-Hézode, Suzanne McGoey, Damien Sternberg, et al.
Multiple Sclerosis and Related Disorders|April 22, 2020
Multiple cervical dissections after RituximabThomas Roux, Savine Vicart, Natalia Shor, et al.
Pediatric Neurology|June 14, 2023
Care Recommendations for the Investigation and Management of Children With Skeletal Muscle ChannelopathiesEmma Matthews, Jacqueline Palace, Sithara Ramdas, et al.
Muscle & Nerve|November 3, 2009
Homozygosity for dominant mutations increases severity of muscle channelopathiesMarianne Arzel-Hézode, Damien Sternberg, Nacira Tabti, et al.
Annals of Neurology|September 25, 2004
Electromyography guides toward subgroups of mutations in muscle channelopathiesEmmanuel Fournier, Marianne Arzel, Damien Sternberg, et al.
Journal of the Neurological Sciences|March 18, 2019
Early radiological features of severe longitudinally extensive transverse myelitis over timeSamuel Cattan, Caroline Papeix, David Grabli, et al.
Scientific Reports|November 14, 2018
A204E mutation in Na<sub>v</sub>1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signsYosuke Kokunai, Carine Dalle, Savine Vicart, et al.
Scientific Reports|February 3, 2018
Substitutions of the S4DIV R2 residue (R1451) in Na<sub>V</sub>1.4 lead to complex forms of paramyotonia congenita and periodic paralysesHugo Poulin, Pascal Gosselin-Badaroudine, Savine Vicart, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Journal of Neuromuscular Diseases|December 16, 2020
Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision MedicineJean-François Desaphy, Concetta Altamura, Savine Vicart, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 31, 2007
Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorderBertrand Fontaine, Emmanuel Fournier, Damien Sternberg, et al.
Neuromuscular Disorders : NMD|February 10, 2009
Glucocorticoids may trigger attacks in several types of periodic paralysisMarianne Arzel-Hézode, Suzanne McGoey, Damien Sternberg, et al.
Multiple Sclerosis and Related Disorders|April 22, 2020
Multiple cervical dissections after RituximabThomas Roux, Savine Vicart, Natalia Shor, et al.
Pediatric Neurology|June 14, 2023
Care Recommendations for the Investigation and Management of Children With Skeletal Muscle ChannelopathiesEmma Matthews, Jacqueline Palace, Sithara Ramdas, et al.
Muscle & Nerve|November 3, 2009
Homozygosity for dominant mutations increases severity of muscle channelopathiesMarianne Arzel-Hézode, Damien Sternberg, Nacira Tabti, et al.
Annals of Neurology|September 25, 2004
Electromyography guides toward subgroups of mutations in muscle channelopathiesEmmanuel Fournier, Marianne Arzel, Damien Sternberg, et al.
Journal of the Neurological Sciences|March 18, 2019
Early radiological features of severe longitudinally extensive transverse myelitis over timeSamuel Cattan, Caroline Papeix, David Grabli, et al.
Scientific Reports|November 14, 2018
A204E mutation in Na<sub>v</sub>1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signsYosuke Kokunai, Carine Dalle, Savine Vicart, et al.
Scientific Reports|February 3, 2018
Substitutions of the S4DIV R2 residue (R1451) in Na<sub>V</sub>1.4 lead to complex forms of paramyotonia congenita and periodic paralysesHugo Poulin, Pascal Gosselin-Badaroudine, Savine Vicart, et al.
Pageof 3