Results 11 to 20 of about 3,314 (74)
Rehabilitation in patients with cerebellar ataxias. [PDF]
Cerebellar ataxias comprise a heterogeneous group of diseases characterized by motor and non-motor symptoms, which can be acquired, degenerative, or have a genetic cause, such as spinocerebellar ataxias (SCA).
Chien HF +7 more
europepmc +3 more sources
Conceitos atuais no tratamento das ataxias hereditárias [PDF]
Hereditary ataxias (HA) represents an extensive group of clinically and genetically heterogeneous neurodegenerative diseases, characterized by progressive ataxia combined with extra-cerebellar and multi-systemic involvements, including peripheral ...
Sheng-Han; Marcondes Junior +6 more
core +7 more sources
Spinocerebellar Ataxia Type 2 [PDF]
1. Introduction: The autosomal dominant cerebellar ataxias (ADCA) are a clinically, pathologically and genetically heterogeneous group of neurodegenerative disorders caused by degeneration of cerebellum and its afferent and efferent connections.
Georg Auburger +9 more
core +1 more source
Ataxias espinocerebelares tipo 2 e tipo 3 : uma perspectiva evolutiva [PDF]
As Ataxias Espinocerebelares tipo 2 (SCA2) e tipo 3 ou doença de Machado Joseph (SCA3/DMJ) fazem parte de um grupo de doenças autossômicas dominantes neurodegenerativas conhecidas como poliglutaminopatias, causadas por expansões de sequências repetitivas
Sena, Lucas Schenatto de
core +1 more source
Epidemiology of inherited cerebellar ataxias and challenges in clinical research [PDF]
Cerebellar ataxia is a clinically heterogeneous group of disorders, which includes several well-characterized genetic diseases as well as sporadic ataxias.
Pilotto, Federica +3 more
core +2 more sources
Análise molecular e clínica das ataxias espinocerebelares [PDF]
As ataxias espinocerebelares dominantes (SCAs), do inglês spinocerebellar ataxia, são um complexo grupo de doenças neurodegenerativas que afetam o cerebelo e suas principais conexões. O início das SCAs ocorre geralmente na vida adulta apresentando grande
Alexis Trott, Trott, Alexis
core +1 more source
The neurological update: therapies for cerebellar ataxias in 2020. [PDF]
Cerebellar ataxias (CAs) represent a heterogeneous group of sporadic or inherited disorders. The clinical spectrum of CAs is continuously expanding. Our understanding of the mechanisms leading to the clinical deficits has improved over these last decades,
Feil, K +4 more
core +2 more sources
Sleep disorders in cerebellar ataxias [PDF]
Cerebellar ataxias comprise a wide range of etiologies leading to central nervous system-related motor and non-motor symptoms. Recently, a large body of evidence has demonstrated a high frequency of non-motor manifestations in cerebellar ataxias ...
Prado, Lucila Bizari Fernandes do [UNIFESP] +13 more
core +1 more source
Paula Coutinho’s outstanding contribution to the definition of Machado-Joseph disease
Machado-Joseph disease, also known as spinocerebellar ataxia type 3, is the most common form of autosomal dominant ataxia in the world. Paula Coutinho, a highly-regarded Portuguese neurologist worldwide, had a seminal participation in the definition of ...
Bruno Carniatto Marques Garcia +4 more
doaj +1 more source
PURPOSE OF REVIEW: The term 'cerebellar ataxias' encompasses the various cerebellar disorders encountered during daily practice. Patients exhibit a cerebellar syndrome and can also present with pigmentary retinopathy, extrapyramidal movement disorders ...
Manto, Mario, Marmolino, Daniele
core +1 more source

