Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
CAPOS syndrome | Semantic Scholar
Clinical features of 10 patients from three families with CAPOS syndrome | 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
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear Auditory neuropathy in pediatr
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
PDF) CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation
Parkinsonism & Related Disorders on Twitter: "#Dystonia #deafness #ATP1A3 # CAPOS Log in to: https://t.co/OaOj1URbYq https://t.co/xQ0wsK7k1g" / Twitter
What is ATP1A3 Gene CAPOS syndrome NGS Genetic DNA Test ?
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear | Revista Portuguesa de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço
Novel pregnancy‐triggered episodes of CAPOS syndrome - Chang - 2018 - American Journal of Medical Genetics Part A - Wiley Online Library
CAPOS syndrome | Semantic Scholar
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome - ScienceDirect
RareConnect - Publicaciones | Facebook
Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorineural Hearing Loss Syndrome
Frontiers | Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype–Phenotype Study and CI Management
The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene
D-DEMØ, a distinct phenotype caused by ATP1A3 mutations | Neurology Genetics
PDF) A novel recurrent mutation in ATP1A3 causes CAPOS syndrome
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases - ScienceDirect
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
Parkinsonism & Related Disorders
A novel recurrent mutation in ATP1A3 causes CAPOS syndrome | Orphanet Journal of Rare Diseases | Full Text
