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Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation.
Blumkin, Lubov; Suls, Arvid; Deconinck, Tine; De Jonghe, Peter; Linder, Ilan; Kivity, Sara; Dabby, Ron; Leshinsky-Silver, Esther; Lev, Dorit; Lerman-Sagie, Tally.
Affiliation
  • Blumkin L; Pediatric Neurology Unit, Wolfson Medical Center, Holon, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Eur J Paediatr Neurol ; 16(4): 356-60, 2012 Jul.
Article in En | MEDLINE | ID: mdl-22169383
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy, Benign Neonatal / Dyskinesias / KCNQ2 Potassium Channel / Myoclonus Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Infant / Male / Newborn / Pregnancy Language: En Journal: Eur J Paediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2012 Document type: Article Affiliation country: Israel Country of publication: Reino Unido
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy, Benign Neonatal / Dyskinesias / KCNQ2 Potassium Channel / Myoclonus Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Infant / Male / Newborn / Pregnancy Language: En Journal: Eur J Paediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2012 Document type: Article Affiliation country: Israel Country of publication: Reino Unido