Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene.

Boysen, Sebastian; Elumalai, Vimala; ElSheikh, Reem H; Aravindhan, Akilandeswari; Veerapandiyan, Aravindhan

Boysen, Sebastian; Elumalai, Vimala; ElSheikh, Reem H; Aravindhan, Akilandeswari; Veerapandiyan, Aravindhan.

Afiliação

Boysen S; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Elumalai V; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
ElSheikh RH; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Aravindhan A; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Veerapandiyan A; Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Electronic address: aveerapandiyan@uams.edu.

J Clin Neurosci ; 100: 212-213, 2022 06.

Article em En | MEDLINE | ID: mdl-35181192

Assuntos

Epilepsia; Paraplegia Espástica Hereditária; Epilepsia/complicações; Epilepsia/genética; Humanos; Proteínas de Membrana/genética; Mutação/genética; Linhagem; Paraplegia Espástica Hereditária/complicações; Paraplegia Espástica Hereditária/genética

Palavras-chave

HSP; Hereditary spastic paraplegia; IGE; Idiopathic generalized epilepsy; NIPA1; SPG6; Spastic paraplegia 6

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Epilepsia Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google