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The progression rate of spinocerebellar ataxia type 2 changes with stage of disease
Rede Neurogenetica
Hospital de Clínicas de Porto Alegre
Faculdade de Medicina de São José do Rio Preto
Setor de Neurologia Geral e Ataxias. Disciplina de Neurologia Clínica da UNIFESP - Escola Paulista de Medicina
Laboratório de Epidemiologia de Malformações Congênitas
Grupo de Pesquisa e Pós-Graduação Hospital de Clínicas de Porto Alegre
Departamento de Estatística
extern
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Keyphrases
Disease Duration
100%
Disease Stage
100%
Progression Rate
100%
Spinocerebellar Ataxia Type 2
100%
Ataxia
62%
Duration Models
50%
Spinocerebellar Ataxia
37%
Neurological Examination
37%
Examination Scores
37%
Clinical Trials
12%
Cognitive Decline
12%
Natural History
12%
Inclusion Criteria
12%
Ataxia Score
12%
Disease Progression
12%
Age of Onset
12%
Slow Progression
12%
Individual Life
12%
Parkinsonism
12%
Dystonic
12%
Multiple Symptoms
12%
Amyotrophy
12%
Pharmacology, Toxicology and Pharmaceutical Science
Disease Duration
100%
Spinocerebellar Degeneration
100%
Disease
100%
Ataxia
75%
Clinical Trial
12%
Disease Exacerbation
12%
Symptom
12%
Onset Age
12%
Muscle Atrophy
12%
Parkinsonism
12%
Neuroscience
Spinocerebellar Ataxia
100%
Ataxia
75%
Parkinsonism
12%
Muscle Atrophy
12%