Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Orlando G P Barsottini"'
Autor:
Marcio Gadelha Vasconcelos, José Antonio Fiorot Jr, Caroline Sarkovas, Aline Pereira Martins Pinto, Orlando G P Barsottini, Alberto Alain Gabbai
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 64, Iss 2a, Pp 322-325 (2006)
A síndrome de Foix-Chavany-Marie (SFCM) caracteriza-se por apraxia da fala associada à paralisia bilateral da face, palato mole, língua e musculatura da faringe, mas com preservação das funções reflexas e automáticas. Na síndrome de Worster-
Externí odkaz:
https://doaj.org/article/3ac16bbdf52744f0a25458d7c11d04bf
Autor:
Jose Luiz Pedroso, Thiago Cardoso Vale, Julian Letícia de Freitas, Filipe Miranda Milagres Araújo, Alex Tiburtino Meira, Pedro Braga Neto, Marcondes C. França, Vitor Tumas, Hélio A. G. Teive, Orlando G. P. Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 11, Pp 1000-1007 (2023)
Background Hereditary or familial spastic paraplegias (SPG) comprise a group of genetically and phenotypically heterogeneous diseases characterized by progressive degeneration of the corticospinal tracts. The complicated forms evolve with other vario
Externí odkaz:
https://doaj.org/article/c01cdf9fe5124b339a883b1b9be69b80
Autor:
Bruna Gutierres Gambirasio, Rodrigo Matos Amaral, Thiago Yoshinaga Tonholo Silva, Danilo Manuel Cerqueira Costa, Flavio Moura Rezende Filho, Pedro Henrique Reis Caldeira Brant, Marcio Luiz Escorcio-Bezerra, Orlando G P Barsottini, José Luiz Pedroso
Publikováno v:
Practical Neurology. 23:67-70
A 57-year-old man was diagnosed with acute myocardial infarction and Stanford type A aortic dissection that had spread to the common iliac arteries. He underwent a Bentall procedure for vascular repair. Immediately after surgery, he developed numbnes
Autor:
Rubens Paulo Araújo Salomão, José Luiz Pedroso, Maria Thereza Drumond Gama, Lívia Almeida Dutra, Ricardo Horta Maciel, Clécio Godeiro-Junior, Hsin Fen Chien, Hélio A. G. Teive, Francisco Cardoso, Orlando G. P. Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 74, Iss 7, Pp 587-596 (2016)
ABSTRACT Neurodegeneration with brain iron accumulation (NBIA) represents a heterogeneous and complex group of inherited neurodegenerative diseases, characterized by excessive iron accumulation, particularly in the basal ganglia. Common clinical feat
Externí odkaz:
https://doaj.org/article/9b32da0ca1794f2183d590331ff2069e
Autor:
José Luiz Pedroso, Thiago Cardoso Vale, Alex Tiburtino Meira, Pedro Braga-Neto, Orlando G. P. Barsottini, Alberto J. Espay
Publikováno v:
Seminars in neurology.
Movement disorders comprise a heterogeneous and complex group of neurological disorders that increase (hyperkinetic) or decrease (hypokinetic) the speed or amplitude of movements, or disrupt their coordinated sequencing. In this article, we describe
Autor:
Tácio Luis Cavalcante Coradine, Lucas de Oliveira Cantaruti Guida, Pedro Fraiman, Adrialdo José Santos, José Luiz Pedroso, Orlando G P Barsottini
Publikováno v:
Practical Neurology. :pn-2023
A 56-year-old woman developed progressive subacute lower limb weakness with sensory and autonomic abnormalities. She had received a living-donor kidney transplantation 21 years before for end-stage chronic kidney disease and took mycophenolate mofeti
Autor:
Alex Tiburtino, Meira, Gustavo L, Franklin, Matheus G, Ferreira, Alberto R M, Martinez, Marcondes C, França, José Luiz, Pedroso, Orlando G P, Barsottini, Hélio A G, Teive
Publikováno v:
Cerebellum (London, England). 21(4)
Autor:
Felipe Franco, da Graça, Thiago M, Peluzzo, Luciana Cardoso, Bonadia, Alberto Rolim Muro, Martinez, Fabricio, Diniz de Lima, José Luiz, Pedroso, Orlando G P, Barsottini, Maria Thereza Drummond, Gama, Fulya, Akçimen, Patrick A, Dion, Guy A, Rouleau, Wilson, Marques, Marcondes Cavalcante, França
Publikováno v:
Cerebellum (London, England). 21(1)
Previous studies using whole exome sequencing (WES) have shown that a significant proportion of adult patients with undiagnosed ataxia in European and North American cohorts have a known genetic cause. Little is known about the diagnostic yield of WE
Publikováno v:
DeckerMed Medicine.
Autor:
José Luiz Pedroso, Priscilla Proveti, Luiz Fernando Teixeira, Juliana Maria Ferraz Sallum, Orlando G. P. Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 10, Pp 816-817 (2014)
Externí odkaz:
https://doaj.org/article/79916ef1d82145618026306fd03171ad