Associated Papers
Serial magnetic resonance imaging findings during severe attacks of familial hemiplegic migraine type 2: a case report.
Fear D et al.
Bmc Neurology, 2021
Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.
Du Y et al.
Neuropediatrics, 2020
Epilepsy in hemiplegic migraine: Genetic mutations and clinical implications.
Prontera P et al.
Cephalalgia : an International Journal of Headache, 2018
Familial Hemiplegic Migraine With Asymmetric Encephalopathy Secondary to ATP1A2 Mutation: A Case Series.
Murphy OC et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society, 2018
ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies.
Bennett CA et al.
Neurology. Genetics, 2017
28717674 (PubMed )
Supplement: supp_3.4.e163_Table_e-1.xlsx › Other_neurological_disorders
ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of Disease.
Friedrich T et al.
Frontiers in Physiology, 2016
27445835 (PubMed )
Supplement: Table1.PDF
Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation.
Iizuka T et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2012
Migraine- and dystonia-related disease-mutations of Na+/K+-ATPases: relevance of behavioral studies in mice to disease symptoms and neurological manifestations in humans.
Bøttger P et al.
Neuroscience and Biobehavioral Reviews, 2012
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