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Neurology, ISSN 0028-3878, 11/2012, Volume 79, Issue 21, pp. 2122 - 2124
Objective: Hemiplegic migraine (HM) is a rare subtype of migraine with aura that occurs as a familial or sporadic condition. The 3 culprit genes identified so... 
ATP1A2 | CLINICAL NEUROLOGY | EPILEPSY | Membrane Proteins - genetics | Humans | Adolescent | Female | Male | Migraine with Aura - genetics | Mutation - genetics | Child | Migraine with Aura - diagnosis | Nerve Tissue Proteins - genetics | Index Medicus | Abridged Index Medicus
Journal Article
Journal Article
Journal of Clinical Neurophysiology, ISSN 0736-0258, 01/2018, Volume 35, Issue 1, pp. e3 - e7
INTRODUCTION:Familial hemiplegic migraine (FHM) is a genetic disease with a variable clinical phenotype. The imaging and electroencephalogram (EEG) correlates... 
Familial hemiplegic migraine | ATP1A2 | EEG | Encephalopathy | NEUROSCIENCES | SPREADING DEPRESSION | CLINICAL NEUROLOGY | Index Medicus
Journal Article
Pediatrics, ISSN 0031-4005, 04/2018, Volume 141, Issue Suppl 5, pp. S390 - S394
Mutations in the ATP1A2 gene cause familial hemiplegic migraine type 2, alternating hemiplegia of childhood, and cerebellar function deficits, epilepsy, and... 
PEDIATRICS | ALTERNATING HEMIPLEGIA | CHILDHOOD | MEMANTINE | MIGRAINE | Dextromethorphan - therapeutic use | Hemiplegia - drug therapy | Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors | Excitatory Amino Acid Antagonists - therapeutic use | Sodium-Potassium-Exchanging ATPase - genetics | Epilepsies, Partial - drug therapy | Humans | Ubiquinone - analogs & derivatives | DNA Polymerase gamma - genetics | Male | Mutation, Missense | Attention Deficit Disorder with Hyperactivity - drug therapy | Syndrome | Ubiquinone - therapeutic use | Motor Skills Disorders - drug therapy | Memantine - therapeutic use | Child | Genetic aspects | Diagnosis | Research | Gene mutations | Risk factors | Alternating hemiplegia | Cerebellum | Headache | Intellectual disabilities | Glutamic acid receptors (ionotropic) | Pathogenesis | Hyperactivity | Epilepsy | Cognitive ability | Nervous system | Motors | Glutamic acid receptors | Dextromethorphan | Gene sequencing | ATP1A2 gene | Missense mutation | Coenzyme Q10 | Hemiplegia | Children | Neurological disorders | Seizures | Deficits | Migraine | Attention deficit hyperactivity disorder | N-Methyl-D-aspartic acid receptors | Valproic acid | Memantine | Antagonist drugs | Excitotoxicity | Point mutation | Paresis | Mutation | Glutamatergic transmission | Index Medicus | Abridged Index Medicus
Journal Article
Scientific Reports, ISSN 2045-2322, 02/2016, Volume 6, Issue 1, pp. 22047 - 22047
Journal Article
Brain, ISSN 0006-8950, 2007, Volume 130, Issue 3, pp. 828 - 835
Rapid-onset dystonia-parkinsonism (RDP) (also known as DYT12) is characterized by the abrupt onset of dystonia and parkinsonism and is caused by mutations in... 
parkinsonism | Na+/K+-ATPase | dystonia | ATP1A2 | LINKAGE | FAMILIAL HEMIPLEGIC MIGRAINE | NEUROSCIENCES | ATPIA3 | rapid-onset dystonia-parkinsonism | CLINICAL NEUROLOGY | RDP
Journal Article
Cephalalgia, ISSN 0333-1024, 08/2008, Volume 28, Issue 8, pp. 887 - 891
Familial hemiplegic migraine (FHM) and alternating hemiplegia of childhood (AHC) are severe neurological disorders that share clinical features. Therefore, FHM... 
mutation | CACNA1A | AHC | HM | Mutation | GENE | CHANNEL | NO MUTATIONS | ATP1A2 | TYPE-2 | NEUROSCIENCES | CLINICAL NEUROLOGY | Genetic Predisposition to Disease - genetics | Migraine Disorders - genetics | Twins, Monozygotic - genetics | Hemiplegia - genetics | Humans | Adolescent | Male | Calcium Channels - genetics | Genetic Linkage | Genetic research | Hemiplegia | Genetic aspects | Migraine | Index Medicus
Journal Article
Journal Article