Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novoATP1A2mutation

Author:

de Vries Boukje,Stam Anine H.,Kirkpatrick Martin,Vanmolkot Kaate R.J.,Koenderink Jan B.,van den Heuvel Jeroen J.M.W.,Stunnenberg Bas,Goudie David,Shetty Jay,Jain Vivek,van Vark Judith,Terwindt Gisela M.,Frants Rune R.,Haan Joost,van den Maagdenberg Arn M.J.M.,Ferrari Michel D.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference7 articles.

1. Haploid insufficiency of ATP1A2 encoding the Na+/K+ pump alpha 2 subunit associated with familial hemiplegic migraine type 2;De Fusco;Nat Genet,2003

2. Epilepsy as part of the phenotype associated with ATP1A2 mutations;Deprez;Epilepsia,2008

3. A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred;Fernandez;Headache,2008

4. The international classification of headache disorders, 2nd edition;Headache Classification Committee of the International Headache Society;Cephalalgia,2004

5. Epidemiology of seizure disorders in children;Leviton;Neuroepidemiology,1982

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