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Journal Article
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2015, Volume 52, Issue 1, pp. 56 - 64
Abstract Background ATP1A3 mutations have now been recognized in infants and children presenting with a diverse group of neurological phenotypes, including... 
Pediatrics | Neurology | CAPOS syndrome | ataxia | rapid-onset dystonia-Parkinsonism | dystonia | ATP1A3 | hemiplegia | alternating hemiplegia of childhood | sodium potassium ATPases | FLUNARIZINE | CEREBRAL EDEMA | ALPHA-3 | MIGRAINE | CLINICAL NEUROLOGY | NA/K-ATPASE | DE-NOVO MUTATIONS | CLINICAL-MANIFESTATIONS | GENE | PEDIATRICS | CALCIUM-CHANNEL | Sodium-Potassium-Exchanging ATPase - genetics | Humans | Foot Deformities, Congenital - genetics | Hemiplegia - therapy | Cerebellar Ataxia - physiopathology | Hemiplegia - diagnosis | Hearing Loss, Sensorineural - diagnosis | Foot Deformities, Congenital - physiopathology | Dystonic Disorders - physiopathology | Dystonic Disorders - therapy | Hemiplegia - physiopathology | Child | Optic Atrophy - diagnosis | Optic Atrophy - genetics | Diagnosis, Differential | Dystonic Disorders - genetics | Optic Atrophy - physiopathology | Foot Deformities, Congenital - diagnosis | Foot Deformities, Congenital - therapy | Hearing Loss, Sensorineural - genetics | Reflex, Abnormal - genetics | Optic Atrophy - therapy | Phenotype | Animals | Cerebellar Ataxia - genetics | Cerebellar Ataxia - therapy | Dystonic Disorders - diagnosis | Hearing Loss, Sensorineural - therapy | Hemiplegia - genetics | Mutation | Cerebellar Ataxia - diagnosis | Hearing Loss, Sensorineural - physiopathology | Hemiplegia | Genetic aspects | Parkinson's disease | Dystonia
Journal Article