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Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation.
Oguz Akarsu, Emel; Tekturk, Pinar; Yapici, Zuhal; Tepgec, Fatih; Uyguner, Z Oya; Baykan, Betul.
Affiliation
  • Oguz Akarsu E; Istanbul University, Istanbul Faculty of Medicine, Department of Neurology, Istanbul, Turkey. Electronic address: emeloguz@yahoo.com.
  • Tekturk P; Istanbul University, Istanbul Faculty of Medicine, Department of Neurology, Istanbul, Turkey.
  • Yapici Z; Istanbul University, Istanbul Faculty of Medicine, Department of Neurology, Istanbul, Turkey.
  • Tepgec F; Istanbul University, Istanbul Faculty of Medicine, Department of Medical Genetics, Istanbul, Turkey.
  • Uyguner ZO; Istanbul University, Istanbul Faculty of Medicine, Department of Medical Genetics, Istanbul, Turkey.
  • Baykan B; Istanbul University, Istanbul Faculty of Medicine, Department of Neurology, Istanbul, Turkey.
Seizure ; 42: 49-51, 2016 Nov.
Article in En | MEDLINE | ID: mdl-27723502
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Status Epilepticus / Myoclonic Epilepsies, Progressive / Acid Ceramidase / Mutation Type of study: Risk_factors_studies Limits: Child / Female / Humans Language: En Journal: Seizure Journal subject: NEUROLOGIA Year: 2016 Document type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Status Epilepticus / Myoclonic Epilepsies, Progressive / Acid Ceramidase / Mutation Type of study: Risk_factors_studies Limits: Child / Female / Humans Language: En Journal: Seizure Journal subject: NEUROLOGIA Year: 2016 Document type: Article