✦ LIBER ✦

P169 Variable clinical course in children with severe myoclonic epilepsy of infancy (SMEI) and different mutations in the SCN1A gene

✍ Scribed by N. Barišić; I. Lehman; L. Claes; A. Lofgren; P. De Jonghe

Book ID: 114360037
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 40 KB
Volume: 13
Category: Article
ISSN: 1090-3798
DOI: 10.1016/s1090-3798(09)70227-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Familial Occurrence of Febrile Seizures

Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations

📂 Article 📅 2007 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 72 KB

Familial Occurrence of Febrile Seizures

Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations

✍ Maria Margherita Mancardi; Pasquale Striano; Elena Gennaro; Francesca Madia; Rob 📂 Article 📅 2006 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 283 KB

Mutations of Neuronal Voltage-gated Na+

Mutations of Neuronal Voltage-gated Na+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)

✍ Goryu Fukuma; Hirokazu Oguni; Yukiyoshi Shirasaka; Kazuyoshi Watanabe; Tasuku Mi 📂 Article 📅 2004 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 238 KB

Significant correlation of the SCN1A mut

Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy

✍ Iori Ohmori; Mamoru Ouchida; Yoko Ohtsuka; Eiji Oka; Kenji Shimizu 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 229 KB

Clinical correlations of mutations in th

Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy

✍ Berten P.G.M Ceulemans; Lieve R.F Claes; Lieven G Lagae 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 170 KB

De Novo Mutations in the Sodium-Channel

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

✍ Claes, Lieve (author);Del-Favero, Jurgen (author);Ceulemans, Berten (author);Lag 📂 Article 📅 2001 🏛 American Society of Human Genetics 🌐 English ⚖ 799 KB