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» Authors » Orlando G P Barsottini

Orlando G P Barsottini

Explore the profile of Orlando G P Barsottini including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 104
Citations 425
Followers 0
Related Specialties
Neurology
Psychiatry
Neurosurgery
Top 10 Co-Authors
Jose Luiz Pedroso
Pedro Braga-Neto
Andre C Felicio
Helio A G Teive
Livia Almeida Dutra
Paulo Victor Sgobbi de Souza
Flavio Moura Rezende Filho
Thiago Cardoso Vale
Marcondes Cavalcante Franca Jr
Clecio Godeiro-Junior
Published In
Arq Neuropsiquiatr
Mov Disord
Neurology
Parkinsonism Relat Disord
Cerebellum
Affiliations
Soon will be listed here.
Recent Articles
1.
Teaching Video NeuroImage: Minipolymyoclonus: A Clinical Clue to Spinal Muscular Atrophy
Albuquerque Filho J, Fraiman P, Barsottini O, Pedroso J, Fonseca A
Neurology . 2025 Jan; 104(4):e213364. PMID: 39823547
No abstract available.
2.
Visual allesthesia as manifestation of migraine aura
Lima M, Pedroso J, Barsottini O, Rezende Filho F
Pract Neurol . 2024 Dec; 25(2):174-175. PMID: 39626962
No abstract available.
3.
Teaching Video Neuroimage: Speech-Induced Mouth Dystonia in SCA2
Vale T, Ferraz H, Barsottini O, Pedroso J
Neurology . 2024 Nov; 103(12):e210099. PMID: 39586053
No abstract available.
4.
Natural History of Dystonia in SYNE1 Ataxia: A Clinical, Imaging and Neurophysiological Observation
Jaques C, Gama M, de Oliveira R, Rezende T, Silva T, Franca Jr M, et al.
Mov Disord Clin Pract . 2024 Oct; 12(1):100-104. PMID: 39382210
No abstract available.
5.
Acute spinal cord compression due to extramedullary haematopoiesis
Barreto M, Correia J, de Moraes M, da Silva N, Pedroso J, Barsottini O
Pract Neurol . 2024 Oct; 25(1):82-83. PMID: 39353731
No abstract available.
6.
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study
Rezende T, Adanyaguh I, Barsottini O, Bender B, Cendes F, Coutinho L, et al.
J Neurol Neurosurg Psychiatry . 2024 Feb; 95(7):682-690. PMID: 38383154
Background: Spinal cord damage is a feature of many spinocerebellar ataxias (SCAs), but well-powered in vivo studies are lacking and links with disease severity and progression remain unclear. Here we...
7.
Teaching Video NeuroImage: Mutation Causes Chronic Progressive External Ophthalmoplegia and Cerebellar Ataxia: A POLG-Like Phenotype
Fraiman P, Silva T, Pedroso J, Barsottini O
Neurology . 2024 Feb; 102(5):e209186. PMID: 38315955
No abstract available.
8.
Cranial Nerve Thinning Distinguishes RFC1-Related Disorder from Other Late-Onset Ataxias
Lobo C, Wertheimer G, Schmitt G, Matos P, Rezende T, Silva J, et al.
Mov Disord Clin Pract . 2024 Jan; 11(1):45-52. PMID: 38291837
Background: RFC1-related disorder (RFC1/CANVAS) shares clinical features with other late-onset ataxias, such as spinocerebellar ataxias (SCA) and multiple system atrophy cerebellar type (MSA-C). Thinning of cranial nerves V (CNV) and...
9.
Fragile X premutation mimicking late onset hereditary spastic paraplegia
Fraiman P, Silva T, Marussi V, de Oliveira J, Barsottini O, Pedroso J
Parkinsonism Relat Disord . 2024 Jan; 119:105964. PMID: 38177000
No abstract available.
10.
Expanding the phenotypic spectrum of -related leucoencephalopathy and ataxia
Nobrega P, R B de Paiva A, Souza K, de Souza J, Lima P, da Silva D, et al.
Brain Commun . 2024 Jan; 6(1):fcad273. PMID: 38173802
Mutations in are a rare cause of autosomal recessive leucoencephalopathy with ataxia and specific imaging abnormalities. Very few cases have been reported to date. Here, we describe the clinical and...