Zobrazeno 1 - 10
of 196
pro vyhledávání: '"Wladimir Bocca Vieira de Rezende, Pinto"'
Autor:
Marco Orsini, Wladimir Bocca Vieira de Rezende Pinto, Paulo Sgobbi, Acary Souza Bulle Oliveira
Publikováno v:
Muscles, Vol 3, Iss 3, Pp 235-241 (2024)
A 72-year-old Brazilian woman presented with a 4-year history of rest tremors of the hands, followed by slowness of movement, and a diagnosis of idiopathic Parkinson’s disease. She was started on dopamine agonists with significant improvement. Afte
Externí odkaz:
https://doaj.org/article/743cb75900424bc4a85aa0cb56df1830
Autor:
Paulo de Lima Serrano, Thaiane de Paulo Varollo Rodrigues, Leslyê Donato Pinto, Indiara Correia Pereira, Igor Braga Farias, Renan Brandão Rambaldi Cavalheiro, Patrícia Marques Mendes, Kaliny Oliveira Peixoto, João Paulo Barile, Daniel Delgado Seneor, Eduardo Gleitzmann Correa Silva, Acary Souza Bulle Oliveira, Wladimir Bocca Vieira de Rezende Pinto, Paulo Sgobbi
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 5, Pp 4309-4323 (2024)
Leukodystrophies represent a large and complex group of inherited disorders affecting the white matter of the central nervous system. Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a rare leukodystrophy which still
Externí odkaz:
https://doaj.org/article/d3771228b9ee4469b6ffb34d490f9b85
Autor:
Paulo Sgobbi, Igor Braga Farias, Paulo de Lima Serrano, Bruno de Mattos Lombardi Badia, Hélvia Bertoldo de Oliveira, Alana Strucker Barbosa, Camila Alves Pereira, Vanessa de Freitas Moreira, Marco Antônio Troccoli Chieia, Adriel Rêgo Barbosa, Pedro Henrique Almeida Fraiman, Vinícius Lopes Braga, Roberta Ismael Lacerda Machado, Sophia Luiz Calegaretti, Isabela Danziato Fernandes, Roberta Correa Ribeiro, Marco Antonio Orsini Neves, Wladimir Bocca Vieira de Rezende Pinto, Acary Souza Bulle Oliveira
Publikováno v:
Muscles, Vol 3, Iss 1, Pp 4-15 (2024)
An 18-year-old man presented with slowly progressive infancy-onset spasticity of the lower limbs and cerebellar ataxia, associated with painless strabismus, intellectual disability, urinary incontinence, bilateral progressive visual loss, and cogniti
Externí odkaz:
https://doaj.org/article/2a0b634e5cd440ce9ec3c9e42072fe9c
Autor:
Paulo Sgobbi, Paulo de Lima Serrano, Bruno de Mattos Lombardi Badia, Igor Braga Farias, Hélvia Bertoldo de Oliveira, Alana Strucker Barbosa, Camila Alves Pereira, Vanessa de Freitas Moreira, Ícaro França Navarro Pinto, Acary Souza Bulle Oliveira, Wladimir Bocca Vieira de Rezende Pinto
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundAcute hepatic porphyrias (AHP) represent a rare group of inherited metabolic disorders of heme biosynthesis pathway. This study aims to determine the diagnostic and prognostic value of serum neurofilament light chain (NfL) as potential biom
Externí odkaz:
https://doaj.org/article/33e19679dfe04101aeedd133779ded9c
Autor:
Francisco de Assis Aquino Gondim, Wladimir Bocca Vieira de Rezende Pinto, Marco Antônio Troccoli Chieia, Carolina da Cunha Correia, Francisco Marcos Bezerra Cunha, Mário Emílio Teixeira Dourado Jr, Marcondes Cavalcante França Júnior, Wilson Marques Júnior, Acary Souza Bulle Oliveira, Cleonisio Leite Rodrigues, Delson José da Silva, Elza Dias-Tosta
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 08, Pp 764-775 (2023)
The spectrum of neuropsychiatric phenomena observed in amyotrophic lateral sclerosis (ALS) is wide and not fully understood. Disorders of laughter and crying stand among the most common manifestations. The aim of this study is to report the results o
Externí odkaz:
https://doaj.org/article/70f2d0adf5444da089fc3fc57b5930c6
Autor:
Paulo Victor Sgobbi Souza, Gliciane Afonso, Wladimir Bocca Vieira de Rezende Pinto, Paulo de Lima Serrano, Bruno de Mattos Lombardi Badia, Igor Braga Farias, Ana Carolina dos Santos Jorge, Roberta Ismael Lacerda Machado, Icaro França Navarro Pinto, Glenda Barbosa Barros, Helvia Bertoldo de Oliveira, Samia Rogatis Calil, Cibele Franz, Acary Souza Bulle Oliveira
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-11 (2023)
Abstract Background Porphyrias are a rare group of disease due to inherited defects of heme synthesis with important systemic manifestations and great burden of disease for patients and families due to the exceptional course of disease with disabling
Externí odkaz:
https://doaj.org/article/e991abfc8f334db599cba5bf626ab962
Autor:
Vinícius Lopes Braga, Heloísa Lopes Cohim Moreira, Pedro Henrique Almeida Fraiman, Filipe Pereira Sarmento, Igor Braga Farias, Paulo de Lima Serrano, Bruno de Mattos Lombardi Badia, Marco Antônio Troccoli Chieia, Wladimir Bocca Vieira de Rezende Pinto, Paulo Victor Sgobbi de Souza, Acary Souza Bulle Oliveira
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 02, Pp 001-002 (2024)
Externí odkaz:
https://doaj.org/article/5f6cacd5a1db4de191c7858a30c4234b
Autor:
Wladimir Bocca Vieira de Rezende Pinto, Acary Souza Bulle Oliveira, Alzira Alves de Siqueira Carvalho, Hasan Orhan Akman, Paulo Victor Sgobbi de Souza
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/a5f49d73d2fc412896b18f25e9af8e39
Autor:
Paulo Ribeiro Nóbrega, Anderson Moura Bernardes, Rodrigo Mariano Ribeiro, Sophia Costa Vasconcelos, David Augusto Batista Sá Araújo, Vitor Carneiro de Vasconcelos Gama, Helena Fussiger, Carolina de Figueiredo Santos, Daniel Aguiar Dias, André Luíz Santos Pessoa, Wladimir Bocca Vieira de Rezende Pinto, Jonas Alex Morales Saute, Paulo Victor Sgobbi de Souza, Pedro Braga-Neto
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Cerebrotendinous Xanthomatosis represents a rare and underdiagnosed inherited neurometabolic disorder due to homozygous or compound heterozygous variants involving the CYP27A1 gene. This bile acid metabolism disorder represents a key potentially trea
Externí odkaz:
https://doaj.org/article/0efb18fac58149eaa7184750e1d73b5b
Autor:
Fabiano Ferreira Abrantes, Marianna Pinheiro Moraes de Moraes, José Marcos Vieira de Albuquerque Filho, Jéssica Monique Dias Alencar, Alexandre Bussinger Lopes, Wladimir Bocca Vieira de Rezende Pinto, Paulo Victor Sgobbi de Souza, Enedina Maria Lobato de Oliveira, Acary de Souza Bulle de Oliveira, José Luiz Pedroso, Orlando Graziani Povoas Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 79, Iss 11, Pp 1012-1025 (2021)
ABSTRACT For patients with autoimmune diseases, the risks and benefits of immunosuppressive or immunomodulatory treatment are a matter of continual concern. Knowledge of the follow-up routine for each drug is crucial, in order to attain better outcom
Externí odkaz:
https://doaj.org/article/22e601a560514b1da3c826a1c2c3144c