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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
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
Nephrology Dialysis Transplantation, ISSN 0931-0509, 3/2008, Volume 23, Issue 3, pp. 827 - 833
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2015, Volume 23, Issue 5, pp. 639 - 645
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 11/2008, Volume 17, Issue 21, pp. 3318 - 3331
Journal Article
HEADACHE, ISSN 0017-8748, 01/2008, Volume 48, Issue 1, pp. 101 - 108
Objective. - We studied a large Irish Caucasian pedigree with familial hemiplegic migraine (FHM) with the aim of finding the causative gene mutation.... 
COMMON FORMS | familial hemiplegic migraine | CACNA1A GENE | SPREADING DEPRESSION | CLINICAL NEUROLOGY | REGION | ATP1A2 gene mutation | TYPICAL MIGRAINE | SUSCEPTIBILITY LOCUS | AURA | TYPE-2 | CALCIUM-CHANNEL | CHROMOSOME 19P13
Journal Article