Sodium channel myotonia may be associated with high-risk brief resolved unexplained events.

Cea, Gabriel; Andreu, Daniel; Fletcher, Elaine; Ramdas, Sithara; Sud, Richa; Hanna, Michael G; Matthews, Emma

Cea, Gabriel; Andreu, Daniel; Fletcher, Elaine; Ramdas, Sithara; Sud, Richa; Hanna, Michael G; Matthews, Emma.

Afiliação

Cea G; Departamento de Ciencias Neurológicas, Universidad de Chile, Santiago, Chile.
Andreu D; Servicio de Neurología, Hospital Salvador, Santiago, Chile.
Fletcher E; Departamento de Ciencias Neurológicas, Universidad de Chile, Santiago, Chile.
Ramdas S; Department of Clinical Genetics, Centre for Genomic and Experimental Medicine, Western General Hospital, Edinburgh, EH5 2GL, UK.
Sud R; Department of Paediatric Neurology, John Radcliffe Hospital NHS Foundation Trust, Oxford, UK.
Hanna MG; Neurogenetics Unit, UCL Queen Square Institute of Neurology, London, UK.
Matthews E; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.

Wellcome Open Res ; 5: 57, 2020.

Article em En | MEDLINE | ID: mdl-32509969

Palavras-chave

Apnoea; Channelopathy; Laryngospasm; Muscle Disease; Myotonia; Paediatric; Sodium channel; Stridor

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

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