✦ LIBER ✦

A Case of Familial Hemiplegic Migraine Associated With a Novel ATP1A2 Gene Mutation

✍ Scribed by Angela De Cunto; Marco Bensa; Alessandra Tonelli

Book ID: 119344741
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 416 KB
Volume: 47
Category: Article
ISSN: 0887-8994
DOI: 10.1016/j.pediatrneurol.2012.04.012

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel ATP1A2 gene mutation in familial

A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy

✍ Costa, C.; Prontera, P.; Sarchielli, P.; Tonelli, A.; Bassi, M. T.; Cupini, L. M 📂 Article 📅 2013 🏛 John Wiley and Sons 🌐 English ⚖ 238 KB

A Novel ATP1A2 Gene Mutation in an Irish

A Novel ATP1A2 Gene Mutation in an Irish Familial Hemiplegic Migraine Kindred

✍ Desiree M. Fernandez; Collette K. Hand; Brian J. Sweeney; Nollaig A. Parfrey 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 224 KB

ATP1A2 mutations in 11 families with fam

ATP1A2 mutations in 11 families with familial hemiplegic migraine

✍ Florence Riant; Maurizio De Fusco; Paolo Aridon; Anne Ducros; Claire Ploton; Flo 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 497 KB

Familial hemiplegic migraine (FHM) is an autosomal dominant form of migraine with aura. The disease is caused by mutations of at least three genes among which two have been identified, CACNA1A and ATP1A2. Very few mutations have been identified so far in ATP1A2. We screened the coding sequence of AT

Prolonged Sporadic Hemiplegic Migraine A

Prolonged Sporadic Hemiplegic Migraine Associated With a Novel De Novo Missense ATP1A2 Gene Mutation

✍ Sara De Sanctis; Gaetano Salvatore Grieco; Luciana Breda; Carlo Casali; Manuela 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 182 KB

Alternating hemiplegia of childhood or f

Alternating hemiplegia of childhood or familial hemiplegic migraine?: A novel ATP1A2 mutation

✍ Kathryn J. Swoboda; Emmanuel Kanavakis; Athina Xaidara; Justine E. Johnson; Mark 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 171 KB 👁 2 views

A Novel NaV1.1 Mutation L1613P Associate

A Novel NaV1.1 Mutation L1613P Associated with Familial Hemiplegic Migraine

✍ Fan, Chunxiang; Lehmann-Horn, Frank; Jurkat-Rott, Karin 📂 Article 📅 2014 🏛 Biophysical Society 🌐 English ⚖ 44 KB