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Estacionário rodovia ficção capos syndrome cimento Íngreme raiz

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 (CAPOS): a new syndrome. - Abstract - Europe PMC

NEURIMMINFL2014000778 1..3
NEURIMMINFL2014000778 1..3

PDF) CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation
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
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar

Clinical features of 10 patients from three families with CAPOS syndrome | Download Table
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
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
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear Auditory neuropathy in pediatr

D-DEMØ, a distinct phenotype caused by ATP1A3 mutations | Neurology Genetics
D-DEMØ, a distinct phenotype caused by ATP1A3 mutations | Neurology Genetics

RareConnect - Publicaciones | Facebook
RareConnect - Publicaciones | Facebook

De novo ATP1A3 variants cause polymicrogyria | Science Advances
De novo ATP1A3 variants cause polymicrogyria | Science Advances

Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome - ScienceDirect
Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome - ScienceDirect

ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases - ScienceDirect
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
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC

Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar

Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorineural Hearing Loss Syndrome
Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorineural Hearing Loss Syndrome

A new case of CAPOS/CAOS syndrome | Neurología (English Edition)
A new case of CAPOS/CAOS syndrome | Neurología (English Edition)

Novel pregnancy‐triggered episodes of CAPOS syndrome - Chang - 2018 - American Journal of Medical Genetics Part A - Wiley Online Library
Novel pregnancy‐triggered episodes of CAPOS syndrome - Chang - 2018 - American Journal of Medical Genetics Part A - Wiley Online Library

A new case of CAPOS/CAOS syndrome
A new case of CAPOS/CAOS syndrome

PDF) A novel recurrent mutation in ATP1A3 causes CAPOS syndrome
PDF) A novel recurrent mutation in ATP1A3 causes CAPOS syndrome

Genes | Free Full-Text | Review of Ocular Manifestations of Joubert Syndrome
Genes | Free Full-Text | Review of Ocular Manifestations of Joubert Syndrome

RareConnect - 🔎We're looking for people affected by any of... | Facebook
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
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report - ScienceDirect

CAPOS syndrome | Semantic Scholar
CAPOS syndrome | Semantic Scholar

Desperate Parents Launch Campaign For Rare Disease Toddler Treatment ⋆ Madrid Metropolitan
Desperate Parents Launch Campaign For Rare Disease Toddler Treatment ⋆ Madrid Metropolitan

Frontiers | Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype–Phenotype Study and CI Management
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
The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene