User profiles for O.G.P. Barsottini

Orlando Barsottini

Universidade Federal de Sao Paulo - Departamento de Neurologia e Neurocirurgia
Verified email at unifesp.br
Cited by 5407

Neurological complications in patients with SARS-CoV-2 infection: a systematic review

…, SM Almeida, OGP Barsottini… - Arquivos de Neuro …, 2020 - SciELO Brasil
SciELO - Brasil - Neurological complications in patients with SARS-CoV-2 infection: a systematic
review Neurological complications in patients with SARS-CoV-2 infection: a systematic …

[HTML][HTML] Autoimmune encephalitis: a review of diagnosis and treatment

…, FF Toso, JL Pedroso, OGP Barsottini… - Arquivos de neuro …, 2018 - SciELO Brasil
Autoimmune encephalitis (AIE) is one of the most common causes of noninfectious
encephalitis. It can be triggered by tumors, infections, or it may be cryptogenic. The neurological …

Nonmotor and extracerebellar features in Machado‐Joseph disease: a review

…, I Lopes‐Cendes, OGP Barsottini - Movement …, 2013 - Wiley Online Library
Spinocerebellar ataxia type 3 or Machado‐Joseph disease is the most common spinocerebellar
ataxia worldwide, and the high frequency of nonmotor manifestations in Machado‐…

Translation and validation into Brazilian version of the Scale of the Assessment and Rating of Ataxia (SARA)

…, LA Dutra, JL Pedroso, OGP Barsottini - Arquivos de neuro …, 2010 - SciELO Brasil
The hereditary ataxias comprise a very large spectrum of genetically determined neurodegenerative
disorders with progressive ataxia as the prominent symptom. In order to measure …

ALS5/SPG11/ KIAA1840 mutations cause autosomal recessive axonal Charcot–Marie–Tooth disease

…, R Massa, PH St George-Hyslop, OGP Barsottini… - Brain, 2016 - academic.oup.com
Charcot–Marie–Tooth disease is a group of hereditary peripheral neuropathies that share
clinical characteristics of progressive distal muscle weakness and atrophy, foot deformities, …

Structural signature of SCA3: from presymptomatic to late disease stages

…, JL Pedroso, OGP Barsottini… - Annals of …, 2018 - Wiley Online Library
Objective Machado–Joseph disease (SCA3/MJD) is the most frequent spinocerebellar
ataxia worldwide and characterized by brainstem, basal ganglia, and cerebellar damage. …

Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness

…, L Kuchař, A Baxová, R Chen, OGP Barsottini… - Nature …, 2015 - nature.com
Blindness due to retinal degeneration affects millions of people worldwide, but many
disease-causing mutations remain unknown. PNPLA6 encodes the patatin-like phospholipase …

Cerebellar cognitive affective syndrome in Machado Joseph disease: core clinical features

…, PHF Bertolucci, AA Gabbai, OGP Barsottini - The Cerebellum, 2012 - Springer
The cerebellum is no longer considered a purely motor control device, and convincing evidence
has demonstrated its relationship to cognitive and emotional neural circuits. The aims of …

Neurologic manifestations of antiphospholipid syndrome

…, LA Dutra, FF Abrantes, FF Toso, OGP Barsottini… - Lupus, 2018 - journals.sagepub.com
Neurological involvement in antiphospholipid antibody syndrome (APS) is common, and its
occurrence increases morbidity and mortality. Patients may present variable neurological …

Neuroimaging in hereditary spastic paraplegias: current use and future perspectives

…, LFR Vasconcellos, JL Pedroso, OGP Barsottini… - Frontiers in …, 2019 - frontiersin.org
Hereditary spastic paraplegias (HSP) are a large group of genetic diseases characterized
by progressive degeneration of the long tracts of the spinal cord, namely the corticospinal …