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Cataplexy in Patients Harboring the KCNMA1 p.N999S Mutation.
Heim, Jennifer; Vemuri, Anusha; Lewis, Sara; Guida, Brandon; Troester, Matthew; Keros, Sotirios; Meredith, Andrea; Kruer, Michael C.
Afiliação
  • Heim J; Pediatric Movement Disorders Program, Barrow Neurological Institute Phoenix Children's Hospital Phoenix Arizona USA.
  • Vemuri A; Pathology Department University of Chicago Medical Center Chicago Illinois USA.
  • Lewis S; Pediatric Movement Disorders Program, Barrow Neurological Institute Phoenix Children's Hospital Phoenix Arizona USA.
  • Guida B; Departments of Child Health, Neurology, Genetics, Cellular & Molecular Medicine University of Arizona College of Medicine Phoenix Phoenix Arizona USA.
  • Troester M; Pediatric Movement Disorders Program, Barrow Neurological Institute Phoenix Children's Hospital Phoenix Arizona USA.
  • Keros S; Departments of Child Health, Neurology, Genetics, Cellular & Molecular Medicine University of Arizona College of Medicine Phoenix Phoenix Arizona USA.
  • Meredith A; Pediatric Epilepsy & Sleep Medicine Program, Barrow Neurological Institute Phoenix Children's Hospital Phoenix Arizona USA.
  • Kruer MC; New York Presbyterian Hospital Weill Cornell Medical Center New York New York City USA.
Mov Disord Clin Pract ; 7(7): 861-862, 2020 Oct.
Article em En | MEDLINE | ID: mdl-33043086
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mov Disord Clin Pract Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mov Disord Clin Pract Ano de publicação: 2020 Tipo de documento: Article