Cerebellar Ataxia
Mostrando 1-12 de 164 artigos, teses e dissertações.
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1. Keeping our balance in cerebellar ataxia: the contribution of neuroimaging to clinical investigation
Radiologia Brasileira. Publicado em: 2022
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2. Pure-Tone Hearing Thresholds and Brainstem Auditory Evoked Potentials in Sporadic Ataxia
Abstract Introduction Spinocerebellar ataxia (SCA) is part of a genetic and clinical heteroge- neous group of neurodegenerative diseases characterized by progressive cerebellar ataxia. Objective To describe the results of audiological and electrophysiological hearing evaluations in patients with sporadic ataxia (SA). Methods A retrospective cross-secti
Int. Arch. Otorhinolaryngol.. Publicado em: 2020-03
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3. Severe Cerebellar Degeneration and Chiari I Malformation - Speculative pathophysiology based on a systematic review
RESUMO OBJETIVO A Malformação de Chiari (MC) tipo I sintomática é tratada através da descompressão da fossa posterior com ou sem duroplastia. Observamos alguns casos com ataxia cerebelar grave concomitante devido à atrofia cerebelar. O objetivo deste estudo é revisar a literatura sobre MC associada à atrofia cerebelar grave e discutir sua possíve
Rev. Assoc. Med. Bras.. Publicado em: 2020-03
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4. Severe amitriptyline poisoning treated successfully with combined hemoperfusion and hemodialysis
RESUMO OBJETIVO A Malformação de Chiari (MC) tipo I sintomática é tratada através da descompressão da fossa posterior com ou sem duroplastia. Observamos alguns casos com ataxia cerebelar grave concomitante devido à atrofia cerebelar. O objetivo deste estudo é revisar a literatura sobre MC associada à atrofia cerebelar grave e discutir sua possíve
Rev. Assoc. Med. Bras.. Publicado em: 2020-03
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5. Constraint-induced movement therapy in a patient with ataxia after cerebellar tumor resection
Resumo Introdução: A terapia por contensão induzida (TCI) é um método atual de reabilitação com intuito de tratar indivíduos com perdas funcionais nos membros superiores. Objetivo: Aplicar o método TCI e avaliar seus efeitos em uma paciente com ataxia após a remoção de tumor cerebelar. Método: Trata-se de um estudo longitudinal de caráter
Fisioter. mov.. Publicado em: 30/05/2019
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6. Acute cerebellar ataxia: differential diagnosis and clinical approach
RESUMO A ataxia cerebelar é um achado comum na prática neurológica e tem uma grande variedade de causas, desde a degeneração cerebelar crônica e lentamente progressiva à lesão cerebelar aguda devido a infarto, edema ou hemorragia, configurando uma verdadeira emergência neurológica. Ataxia cerebelar aguda é uma síndrome que ocorre em menos de 72 h
Arq. Neuro-Psiquiatr.. Publicado em: 2019-03
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7. Cerebellar ataxia as presenting feature of hypothyroidism
SUMMARY Symptoms and signs of the hypothyroidism vary in relation to the magnitude and acuteness of the thyroid hormone deficiency. The usual clinical features are constipation, fatigue, cold intolerance and weight gain. Rarely it can present with neurologic problems like reversible cerebellar ataxia, dementia, peripheral neuropathy, psychosis and coma. Hypo
Arch. Endocrinol. Metab.. Publicado em: 16/02/2016
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8. Ataxia cerebellar idiopática com início muito tardio: uma série de casos brasileiros
RESUMOOs autores apresentam uma série de casos incluindo oito pacientes com ataxia cerebellar de início muito tardio (média de 75,5 anos de idade) apresentando ataxia de marcha, associada à atrofia cerebelar.Método: 26 pacientes adultos com diagnóstico de ataxia cerebelar de início tardio idiopática foram analisados ambulatorialmente e acompanhados r
Arq. Neuro-Psiquiatr.. Publicado em: 2015-11
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9. Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families
OBJECTIVE: Spinocerebellar ataxias are neurodegenerative disorders involving the cerebellum and its connections. There are more than 30 distinct subtypes, 16 of which are associated with an identified gene. The aim of the current study was to evaluate a large group of patients from 104 Brazilian families with spinocerebellar ataxias. METHODS: We studied 150
Clinics. Publicado em: 2012
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10. Kikuchi-Fujimoto disease: an unusual association with acute renal failure
Kikuchi-Fujimoto disease, also known as histiocytic necrotizing lymphadenitis of unknown etiopathogenesis, is a self-limited disease which frequently appears as feverish lymphadenomegaly, thus creating the need for differential diagnosis with lymphoma, systemic lupus erythematosus (SLE), infectious mononucleosis, cat-scratch disease, and toxoplasmosis with l
Brazilian Journal of Infectious Diseases. Publicado em: 2010-12
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11. Clinical and molecular studies in five brazilian cases of Friedreich ataxia
Friedreich ataxia (FRDA), the most common autosomal recessive ataxia, is caused in 94% of cases by homozygous expansions of an unstable GAA repeat localised in intron 1 of the X25 gene. We have investigated this mutation in five Brazilian patients: four with typical FRDA findings and one patient with atypical manifestations, who was considered to have some o
Publicado em: 2010
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12. Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10)
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant neurodegenerative disease characterized by cerebellar ataxia and seizures. The disease is caused by a large ATTCT repeat expansion in the ATXN10 gene. The first families reported with SCA10 were of Mexican origin, but the disease was soon after described in Brazilian families of mixed Portuguese
Publicado em: 2010