Desperate Parents Launch Campaign For Rare Disease Toddler Treatment ⋆ Madrid Metropolitan
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear Auditory neuropathy in pediatr
Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorineural Hearing Loss Syndrome
Fever-related ataxia: a case report of CAPOS syndrome | Cerebellum & Ataxias | Full Text
PDF) A novel recurrent mutation in ATP1A3 causes CAPOS syndrome
A novel recurrent mutation in ATP1A3 causes CAPOS syndrome | Orphanet Journal of Rare Diseases | Full Text
Frontiers | ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
De novo ATP1A3 variants cause polymicrogyria | Science Advances
PDF) Fever-related ataxia: a case report of CAPOS syndrome
Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome - ScienceDirect
Compilation of previously published diagnostic criteria for AHC, RDP,... | Download Table
The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene
Parkinsonism & Related Disorders
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases - ScienceDirect
What is ATP1A3 Gene CAPOS syndrome NGS Genetic DNA Test ?
D-DEMØ, a distinct phenotype caused by ATP1A3 mutations | Neurology Genetics
NEURIMMINFL2014000778 1..3
A new case of CAPOS/CAOS syndrome
RareConnect - Publicaciones | Facebook
Genes | Free Full-Text | Review of Ocular Manifestations of Joubert Syndrome
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
Frontiers | Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype–Phenotype Study and CI Management
PDF) CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation
CAPOS syndrome | Semantic Scholar
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
