Pardal obturador ferro capos syndrome Grande carvalho mistura herdar
Clinical features of 10 patients from three families with CAPOS syndrome | Download Table
rare_diseases_in_pediatric_anesthesia
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear | Revista Portuguesa de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço
CAPOS syndrome | Semantic Scholar
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report - ScienceDirect
NEURIMMINFL2014000778 1..3
PDF) Fever-related ataxia: a case report of CAPOS syndrome
Fever-related ataxia: a case report of CAPOS syndrome | Cerebellum & Ataxias | Full Text
RareConnect - Publicaciones | Facebook
Genes | Free Full-Text | Review of Ocular Manifestations of Joubert Syndrome
De novo ATP1A3 variants cause polymicrogyria | Science Advances
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
A new case of CAPOS/CAOS syndrome | Neurología (English Edition)
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar
Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome - ScienceDirect
PDF) CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar
Frontiers | Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype–Phenotype Study and CI Management
Frontiers | ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum
A novel recurrent mutation in ATP1A3 causes CAPOS syndrome | Orphanet Journal of Rare Diseases | Full Text
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorineural Hearing Loss Syndrome
PDF) A novel recurrent mutation in ATP1A3 causes CAPOS syndrome
Compilation of previously published diagnostic criteria for AHC, RDP,... | Download Table
Desperate Parents Launch Campaign For Rare Disease Toddler Treatment ⋆ Madrid Metropolitan