User profiles for O.G.P. Barsottini
Orlando BarsottiniUniversidade Federal de Sao Paulo - Departamento de Neurologia e Neurocirurgia Verified email at unifesp.br Cited by 5308 |
[HTML][HTML] 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 …
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 …
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‐…
ataxia worldwide, and the high frequency of nonmotor manifestations in Machado‐…
[HTML][HTML] 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 …
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, …
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. …
ataxia worldwide and characterized by brainstem, basal ganglia, and cerebellar damage. …
[HTML][HTML] 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 …
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 …
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 …
occurrence increases morbidity and mortality. Patients may present variable neurological …
[HTML][HTML] 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 …
by progressive degeneration of the long tracts of the spinal cord, namely the corticospinal …