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4 articles related to "Scn4a Gene"

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Articles

Case Report

Published on 30 May 2018

Flecainide-Induced Brugada Syndrome in a Patient With Skeletal Muscle Sodium Channelopathy: A Case Report With Critical Therapeutical Implications and Review of the Literature

in Neuromuscular Disorders and Peripheral Neuropathies

Michele Cavalli
Barbara Fossati
Raffaele Vitale
Elisa Brigonzi
Vito A. G. Ricigliano
Lorenzo Saraceno
Rosanna Cardani
Carlo Pappone
Giovanni Meola

Frontiers in Neurology

doi 10.3389/fneur.2018.00385

4,803 views
17 citations

Original Research

Published on 29 Apr 2020

Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4

in Neuromuscular Disorders and Peripheral Neuropathies

Serena Pagliarani
Sabrina Lucchiari
Marina Scarlato
Elisa Redaelli
Anna Modoni
Francesca Magri
Barbara Fossati
Stefano C. Previtali
Valeria A. Sansone
Marzia Lecchi

Frontiers in Neurology

doi 10.3389/fneur.2020.00255

6,155 views
6 citations

Case Report

Published on 25 Oct 2019

SCN4A p.R675Q Mutation Leading to Normokalemic Periodic Paralysis: A Family Report and Literature Review

in Neuromuscular Disorders and Peripheral Neuropathies

Jiejing Shi
Qianqian Qu
Haiyan Liu
Wenhao Cui
Yan Zhang
Haidong Lv
Zuneng Lu

Frontiers in Neurology

doi 10.3389/fneur.2019.01138

3,979 views
5 citations

Original Research

Published on 29 Jul 2020

Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in SCN4A in a Large Cohort of Italian Patients

in Neuromuscular Disorders and Peripheral Neuropathies

Lorenzo Maggi
Raffaella Brugnoni
Eleonora Canioni
Paola Tonin
Veronica Saletti
Patrizia Sola
Stefano Cotti Piccinelli
Lara Colleoni
Paola Ferrigno
Antonella Pini

Frontiers in Neurology

doi 10.3389/fneur.2020.00646

10,003 views
12 citations