Zobrazeno 1 - 10
of 220
pro vyhledávání: '"Pedro Braga‐Neto"'
Autor:
David Augusto Batista Sá Araújo¹, Rodrigo Mariano Ribeiro, Pedro Lucas Grangeiro Sá Barreto Lima, Dánton Campos de Queiroz, Milena Sales Pitombeira, Bernardo Martins, Pablo Picasso Araújo Coimbra, Cleto Dantas Nogueira, Pedro Braga-Neto, Guilherme Diogo Silva, Paulo Ribeiro Nóbrega
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background To report a case of IgG4-related pachymeningitis presenting with cystic lesions mimicking neurocysticercosis. Case presentation A 40-year-old female patient with tetraparesis, dysphagia and dysphonia was evaluated with clinical ex
Externí odkaz:
https://doaj.org/article/660b8ab7acb646f3a7078347e74ad8e1
Autor:
Danilo Nunes Oliveira, José Wagner Leonel Tavares-Júnior, Werbety Lucas Queiroz Feitosa, Letícia Chaves Vieira Cunha, Carmem Meyve Pereira Gomes, Caroline Aquino Moreira-Nunes, Jean Breno Silveira da Silva, Artur Victor Menezes Sousa, Safira de Brito Gaspar, Emmanuelle Silva Tavares Sobreira, Laís Lacerda Brasil de Oliveira, Raquel Carvalho Montenegro, Maria Elisabete Amaral de Moraes, Manoel Alves Sobreira-Neto, Pedro Braga-Neto
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 09, Pp 001-007 (2024)
Background Olfactory dysfunction (OD) represents a frequent manifestation of the coronavirus disease 2019 (COVID-19). Apolipoprotein E (APOE) is a protein that interacts with the angiotensin-converting enzyme receptor, essential for viral entry into
Externí odkaz:
https://doaj.org/article/f1e7cb31da1a4e4b9c64d323df08be25
Autor:
Breno Kazuo Massuyama, Maria Thereza Drumond Gama, Thiago Yoshinaga Tonholo Silva, Pedro Braga-Neto, José Luiz Pedroso, Orlando Graziani Povoas Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 08, Pp 1-8 (2024)
Background Cerebellar ataxias comprise sporadic and genetic etiologies. Ataxia may also be a presenting feature in hereditary spastic paraplegias (HSPs).
Externí odkaz:
https://doaj.org/article/5c0f1bcc811d4c6d840ddb9659913803
Autor:
Antonio Edvan Camelo-Filho, Pedro Lucas Grangeiro de Sá Barreto Lima, Francisco Luciano Honório Barreto Cavalcante, Pedro Vitor Ferreira Rodrigues, Oliver Reiks Miyajima, Pedro Braga-Neto, Paulo Ribeiro Nóbrega
Publikováno v:
Revista da Sociedade Brasileira de Medicina Tropical, Vol 57 (2024)
ABSTRACT A 34-year-old man developed severe envenomation after being bitten by a Crotalus durissus (rattlesnake), which was treated with anticrotalic serum. Three weeks later, the patient reported paresthesia and neuropathic pain in the left hand, wh
Externí odkaz:
https://doaj.org/article/feeae73ee9cf468e88249f2666a71677
Autor:
Pedro Lucas G S B Lima, Paulo R Nobrega, Fernando Freua, Pedro Braga-Neto, Anderson R B Paiva, Thiago Gonçalves Guimarães, Fernando Kok
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-4 (2024)
Abstract Background Progressive Myoclonic Epilepsy (PME) is a group of rare diseases that are difficult to differentiate from one another based on phenotypical characteristics. Case report We report a case of PME type 7 due to a pathogenic variant in
Externí odkaz:
https://doaj.org/article/6c169e2f170342bb84a318229fa91777
Autor:
Carla Marineli Saraiva do Amaral, Samuel Brito de Almeida, Renata Parente de Almeida, Simony Lira do Nascimento, Rodrigo Mariano Ribeiro, Pedro Braga-Neto
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Introduction Postural balance impairment can affect the quality of life of patients with Parkinson’s disease. Previous studies have described connections of the vestibular system with postural functions, suggesting a potential participatio
Externí odkaz:
https://doaj.org/article/6ce10953bcc8444485444e238289b508
Autor:
Antonio Edvan Camelo-Filho, Pedro Lucas Grangeiro Sá Barreto Lima, Francisco Luciano Honório Barreto Cavalcante, Oliver Reiks Miyajima, Carolina Figueiredo Santos, Rodrigo Fagundes da Rosa, André Luiz Santos Pessoa, Pedro Braga-Neto, Paulo Ribeiro Nóbrega
Publikováno v:
Brain Sciences, Vol 14, Iss 11, p 1159 (2024)
Cerebrotendinous xanthomatosis (CTX) is a rare metabolic disorder caused by mutations in the CYP27A1 gene, leading to cholestanol accumulation in various tissues, including peripheral nerves. Polyneuropathy is an underrecognized feature with consider
Externí odkaz:
https://doaj.org/article/a242ae5464394c13abe6f2b550a213e3
Autor:
Danielle Pessoa Lima, Francisco Abaeté das Chagas-Neto, João Rafael Gomes de Luna, Yasmin de Oliveira Martins, Samuel Brito de Almeida, Camila Ximenes Feitosa, Leticia Brasil Gradvohl, Isabele Dantas Rosa, Fábia Karine de Moura Lopes, Luciana Felipe Férrer Aragão, Antonio Brazil Viana-Júnior, Kristopherson Lustosa Augusto, Jarbas de Sá Roriz-Filho, Catarina Brasil d’Alva, Renan Magalhães Montenegro-Júnior, Pedro Braga-Neto
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundParkinson’s disease (PD) is the second most common neurodegenerative illness and has the highest increase rate in recent years. There is growing evidence to suggest that PD is linked to higher osteoporosis rates and risk of fractures.Obje
Externí odkaz:
https://doaj.org/article/09d34337dbb24acf902ebefb9690d93d
Autor:
Pedro Braga-Neto, Paulo Ribeiro Nobrega, Lívio Leite Barros, Pedro Lucas Grangeiro de Sá Barreto Lima, Pedro Helder de Oliveira Júnior, Daniel Aguiar Dias, Carolina de Figueiredo Santos
Publikováno v:
BMJ Neurology Open, Vol 6, Iss 1 (2024)
Background Wyburn-Mason syndrome is a rare, non-hereditary congenital disease, belonging to the group of neurocutaneous syndromes with fewer than 100 cases reported since its first description in 1937.Case report A young adult man was initially evalu
Externí odkaz:
https://doaj.org/article/7b6f9ade53954c6884b069b542f92625
Autor:
Daniela Cabral de Sousa, Emmanuelle Silva Tavares Sobreira, Werbety Lucas Queiroz Feitosa, Ticiana Maria Pinto Moreira Aires, Leticia Pastuszka Paz Araújo, Andressa Laura Castro Silva, Caroline Brandão Joventino, Nathalia Maria Tomaz Silveira, Adriano José Maia Chaves-Filho, Danielle Silveira Macêdo, Pedro Braga-Neto
Publikováno v:
BMC Neuroscience, Vol 24, Iss 1, Pp 1-12 (2023)
Abstract Background The prevalence and pathophysiological mechanisms of cognitive deficits (CD) Systemic Lupus Erythematosus (SLE) and Rheumatoid arthritis (RA) are very heterogeneous and poorly understood. We characterized CD in patients with SLE co
Externí odkaz:
https://doaj.org/article/7f89090db4954dbd9ea9c1636cf64908