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Orlando Graziani Povoas Barsottini

Federal University of São Paulo

331

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2651

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Commentary: Juvenile Dystonia-Parkinsonism due to DNAJC6 Mutation

2021 Movement Disorders Clinical Practice
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From VUS to AUS: The Connection and the Differences between Genetics and Immune-Mediated Disorders

2021 Movement Disorders
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Brain Damage and Gene Expression Across Hereditary Spastic Paraplegia Subtypes.

2021 Movement Disorders
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PRPS1 Gene Mutation Causes Complex X-Linked Adult-Onset Cerebellar Ataxia in Women

2021 Neurology Genetics
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A Diagnostic Approach to Spastic ataxia Syndromes.

2021 The Cerebellum
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Nystagmus may be the first neurological sign in early stages of spinocerebellar ataxia type 3.

2021 Arquivos De Neuro-psiquiatria
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Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective.

2021 The Cerebellum
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Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias.

2021 Scientific Reports
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The Intersection Between Cerebellar Ataxia and Neuropathy: a Proposed Classification and a Diagnostic Approach.

2021 The Cerebellum
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Does SCA45 Cause Very Late-Onset Pure Cerebellar Ataxia?

2021 Neurology Genetics
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