Parkinsonism & Related Disorders
Frontiers | Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype–Phenotype Study and CI Management
Desperate Parents Launch Campaign For Rare Disease Toddler Treatment ⋆ Madrid Metropolitan
Frontiers | ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum
PDF) Fever-related ataxia: a case report of CAPOS syndrome
CAPOS syndrome | Semantic Scholar
De novo ATP1A3 variants cause polymicrogyria | Science Advances
Fever-related ataxia: a case report of CAPOS syndrome | Cerebellum & Ataxias | Full Text
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
PDF) A novel recurrent mutation in ATP1A3 causes CAPOS syndrome
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear Auditory neuropathy in pediatr
Fever-related ataxia: a case report of CAPOS syndrome | Cerebellum & Ataxias | Full Text
PDF) The Expanding Spectrum of Neurological Phenotypes in Children With ATP1A3 Mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and Beyond | Matthew Sweney - Academia.edu
A new case of CAPOS/CAOS syndrome | Neurología (English Edition)
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases - ScienceDirect
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear | Revista Portuguesa de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço
Parkinsonism & Related Disorders on Twitter: "#Dystonia #deafness #ATP1A3 # CAPOS Log in to: https://t.co/OaOj1URbYq https://t.co/xQ0wsK7k1g" / Twitter
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar
PDF) CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation
Genes | Free Full-Text | Review of Ocular Manifestations of Joubert Syndrome
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
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