Nonmotor and extracerebellar features in Machado-Joseph disease: a review.
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Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit.Epidemiological, clinical, and molecular characterization of Cuban families with spinocerebellar ataxia type 3/Machado-Joseph disease.Ataxin-3 phosphorylation decreases neuronal defects in spinocerebellar ataxia type 3 modelsCAG repeat length does not associate with the rate of cerebellar degeneration in spinocerebellar ataxia type 3.Multiple system atrophy of the cerebellar type: clinical state of the art.Peripheral neuropathy and parkinsonism: a large clinical and pathogenic spectrum.Non-Ataxic Presenting Symptoms of Dominant Ataxias.MR Imaging in Spinocerebellar Ataxias: A Systematic Review.Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.Ataxia in children: early recognition and clinical evaluation.NREM-related parasomnias in Machado-Joseph disease: clinical and polysomnographic evaluation.Psychosis in Machado-Joseph Disease: Clinical Correlates, Pathophysiological Discussion, and Functional Brain Imaging. Expanding the Cerebellar Cognitive Affective Syndrome.Cognition in SCA21 reflects developmental and adult onset cerebellar cognitive affective syndrome.Cognitive dysfunction in spinocerebellar ataxia type 3: variable topographies and patterns.Transplantation of cerebellar neural stem cells improves motor coordination and neuropathology in Machado-Joseph disease mice.Human Olfactory Ensheathing Cell Transplantation Improves Motor Function in a Mouse Model of Type 3 Spinocerebellar Ataxia.Increased sexual arousal in patients with movement disorders.Polysomnography findings in spinocerebellar ataxia type 6.Non-motor and Extracerebellar Features in Spinocerebellar Ataxia Type 2.Fatigue and Its Associated Factors in Spinocerebellar Ataxia Type 3/Machado-Joseph Disease.Neurophysiological studies and non-motor symptoms prior to ataxia in a patient with machado-joseph disease: trying to understand the natural history of brain degeneration.A randomized controlled pilot trial of game-based training in individuals with spinocerebellar ataxia type 3.Expanding the Spectrum of Dopa-Responsive Dystonia (DRD) and Proposal for New Definition: DRD, DRD-plus, and DRD Look-alike.The cerebral metabolic topography of spinocerebellar ataxia type 3.
P2860
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P2860
Nonmotor and extracerebellar features in Machado-Joseph disease: a review.
description
article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Nonmotor and extracerebellar features in Machado-Joseph disease: a review.
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type
label
Nonmotor and extracerebellar features in Machado-Joseph disease: a review.
@en
prefLabel
Nonmotor and extracerebellar features in Machado-Joseph disease: a review.
@en
P2093
P2860
P50
P356
P1433
P1476
Nonmotor and extracerebellar features in Machado-Joseph disease: a review
@en
P2093
Hélio A Teive
Iscia Lopes-Cendes
Laura Bannach Jardim
Marcondes C França
Pedro Braga-Neto
P2860
P304
P356
10.1002/MDS.25513
P407
P50
P577
2013-06-17T00:00:00Z