about
Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in manDopamine transporter imaging using 99mTc-TRODAT-1 SPECT in Parkinson's diseaseProgressive supranuclear palsy: new concepts.Neurosarcoidosis: guidance for the general neurologist.Dopaminergic neuronal imaging in genetic Parkinson's disease: insights into pathogenesisMutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness.A diagnostic approach for neurodegeneration with brain iron accumulation: clinical features, genetics and brain imaging.Sjogren-larsson syndrome: case report and review of neurologic abnormalities and ichthyosis.Nonmotor and extracerebellar features in Machado-Joseph disease: a review.Adult onset sporadic ataxias: a diagnostic challenge.Should spinocerebellar ataxias be included in the differential diagnosis for Huntington's diseases-like syndromes?Milestones in Friedreich ataxia: more than a century and still learning.NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2.Current concepts in the treatment of hereditary ataxias.Spinal Cord Damage in Spinocerebellar Ataxia Type 1.One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia.Sleep disorders in Machado-Joseph disease.Central nervous system vasculitis in adults: An update.Professor Wadia's contributions to neurology and spinocerebellar ataxia type 2.Clinical and epidemiological profiles of non-traumatic myelopathies.Dentatorubro-Pallidoluysian Atrophy (DRPLA) among 700 Families with Ataxia in Brazil.Teaching NeuroImages: Cytomegalovirus infection mimicking a brain tumor in a kidney transplant recipient.NREM-related parasomnias in Machado-Joseph disease: clinical and polysomnographic evaluation.SCA1 patients may present as hereditary spastic paraplegia and must be included in spastic-ataxias group.Psychosis in Machado-Joseph Disease: Clinical Correlates, Pathophysiological Discussion, and Functional Brain Imaging. Expanding the Cerebellar Cognitive Affective Syndrome.Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in ManCognition in SCA21 reflects developmental and adult onset cerebellar cognitive affective syndrome.The cerebellum in Parkinson's disease and Parkinsonism in cerebellar disorders.Cognitive dysfunction in spinocerebellar ataxia type 3: variable topographies and patterns.Differentiation of Parkinson's disease and progressive supranuclear palsy with magnetic resonance imaging: the first Brazilian experience.Spinal cord atrophy in spinocerebellar ataxia type 1.Dyke-Davidoff-Masson syndrome: a combination of clinical and radiological signs not to be missed.PINK1 polymorphism IVS1-7 A-->G, exposure to environmental risk factors and anticipation of disease onset in Brazilian patients with early-onset Parkinson's Disease.Adult onset Alexander disease presenting with progressive spastic paraplegia.Huntington disease and Huntington disease-like in a case series from Brazil.Unusual movement disorders in spinocerebellar ataxias."Hot cross bun" sign resembling multiple system atrophy in a patient with Machado-Joseph disease.Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.Excessive fragmentary myoclonus in Machado-Joseph disease.Venlafaxine induced-myoclonus in a patient with mixed dementia.
P50
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P50
description
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Orlando G. Barsottini
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Orlando G. Barsottini
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Orlando G. Barsottini
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Orlando G P Barsottini
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Orlando G. Barsottini
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Orlando G. Barsottini
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P106
P1153
55879071800
P21
P31
P496
0000-0002-0107-0831
P569
2000-01-01T00:00:00Z