Desperate Parents Launch Campaign For Rare Disease Toddler Treatment ⋆ Madrid Metropolitan
RareConnect - 🔎We're looking for people affected by any of... | Facebook
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report - ScienceDirect
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
A novel recurrent mutation in ATP1A3 causes CAPOS syndrome | Orphanet Journal of Rare Diseases | Full Text
A new case of CAPOS/CAOS syndrome | Neurología (English Edition)
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
Fever-related ataxia: a case report of CAPOS syndrome | Cerebellum & Ataxias | Full Text
D-DEMØ, a distinct phenotype caused by ATP1A3 mutations | Neurology Genetics
Novel pregnancy‐triggered episodes of CAPOS syndrome - Chang - 2018 - American Journal of Medical Genetics Part A - Wiley Online Library
What is ATP1A3 Gene CAPOS syndrome NGS Genetic DNA Test ?
A new case of CAPOS/CAOS syndrome
Genes | Free Full-Text | Review of Ocular Manifestations of Joubert Syndrome
Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorineural Hearing Loss Syndrome
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CAPOS syndrome | Semantic Scholar
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases - ScienceDirect
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear Auditory neuropathy in pediatr
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Clinical features of 10 patients from three families with CAPOS syndrome | Download Table
