Your browser doesn't support javascript.
loading
Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to Therapy.
Ashrafi, Mahmoud Reza; Haghighi, Roya; Badv, Reza Shervin; Ghabeli, Homa; Tavasoli, Ali Reza; Pourbakhtyaran, Elham; Rezaei, Zahra; Mahdieh, Nejat; Mohammadi, Pouria; Heidari, Morteza.
Afiliação
  • Ashrafi MR; Department of Pediatric Neurology, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Haghighi R; Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Badv RS; Department of Pediatric Neurology, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Ghabeli H; Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Tavasoli AR; Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Pourbakhtyaran E; Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran.
  • Rezaei Z; Department of Pediatric Neurology, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Mahdieh N; Cardiogenetic Research Center, Rajaei Cardiovascular Medical, and Research Center, Iran University of Medical Sciences, Tehran, Iran.
  • Mohammadi P; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran. Pouria.mohammaditmu@gmail.com.
  • Heidari M; Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Myelin Disorders Clinic, Tehran University of Medical Sciences, Tehran, Iran. m-heidari@sina.tums.ac.ir.
J Mol Neurosci ; 72(5): 1125-1132, 2022 May.
Article em En | MEDLINE | ID: mdl-35275351
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia Parcial Contínua / Doenças Mitocondriais Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans País/Região como assunto: Asia Idioma: En Revista: J Mol Neurosci Assunto da revista: BIOLOGIA MOLECULAR / NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Irã
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia Parcial Contínua / Doenças Mitocondriais Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans País/Região como assunto: Asia Idioma: En Revista: J Mol Neurosci Assunto da revista: BIOLOGIA MOLECULAR / NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Irã