Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
CAPOS syndrome | Semantic Scholar
Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome - ScienceDirect
Parkinsonism & Related Disorders on Twitter: "#Dystonia #deafness #ATP1A3 # CAPOS Log in to: https://t.co/OaOj1URbYq https://t.co/xQ0wsK7k1g" / Twitter
Compilation of previously published diagnostic criteria for AHC, RDP,... | Download Table
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
RareConnect - 🔎We're looking for people affected by any of... | Facebook
De novo ATP1A3 variants cause polymicrogyria | Science Advances
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear | Revista Portuguesa de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço
Desperate Parents Launch Campaign For Rare Disease Toddler Treatment ⋆ Madrid Metropolitan
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The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene
CAPOS syndrome | Semantic Scholar
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
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Novel pregnancy‐triggered episodes of CAPOS syndrome - Chang - 2018 - American Journal of Medical Genetics Part A - Wiley Online Library
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
RareConnect - Publicaciones | Facebook
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
A new case of CAPOS/CAOS syndrome | Neurología (English Edition)
D-DEMØ, a distinct phenotype caused by ATP1A3 mutations | Neurology Genetics
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar
Genes | Free Full-Text | Review of Ocular Manifestations of Joubert Syndrome
Fever-related ataxia: a case report of CAPOS syndrome | Cerebellum & Ataxias | Full Text
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
