Zobrazeno 1 - 10
of 429
pro vyhledávání: '"Doenças do sistema nervoso"'
Autor:
Vinicius Furtado da Silva Castro, Roberto Teodoro Gurgel de Oliveira, João Daniel Lima dos Santos, Ramon de Souza Mendes, Agábio Diógenes Pessoa Neto, Emanuela Coriolano Fidelix, Mário Emílio Teixeira Dourado Júnior
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 04, Pp 001-007 (2024)
Background Guillain-Barré syndrome (GBS) is the most common cause of acute flaccid paralysis worldwide and can be classified into electrophysiological subtypes and clinical variants.
Externí odkaz:
https://doaj.org/article/b9f1b542f51c429a9219641709f5b4ff
Autor:
Moises Dias, Luiz Felipe Pinto, Marcus Vinícius Pinto, Renata Gervais, Paula Accioli, Gabriela Amorim, Mariana Guedes, Carlos Perez Gomes, Roberto Coury Pedrosa, Márcia Waddington-Cruz
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 04, Pp 001-007 (2024)
Background Hereditary transthyretin amyloidosis (ATTRv) is an inherited, progressive, and fatal disease still largely underdiagnosed. Mutations in the transthyretin (TTR) gene cause the TTR protein to destabilize, misfold, aggregate, and deposit in b
Externí odkaz:
https://doaj.org/article/53989f511b9f4e7ca15a62d8b951e699
Autor:
Miguel Bertelli Ramos, Matheus Machado Rech, João Paulo Mota Telles, Willian Medeiros Moraes, Manoel Jacobsen Teixeira, Eberval Gadelha Figueiredo
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 01, Pp 001-010 (2024)
Background In 2012, the Neurocritical Care Society launched a compilation of protocols regarding the core issues that should be addressed within the first hours of neurological emergencies – the Emergency neurological life support (ENLS).
Externí odkaz:
https://doaj.org/article/56487359a1b54286a4bc6b732a5ac168
Autor:
Eduardo Boiteux Uchôa Cavalcanti, Rita de Cássia Carvalho Leal, Wilson Marques Junior, Osvaldo José Moreira do Nascimento
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 10, Pp 913-921 (2023)
Hereditary motor and sensory neuropathy, also known as Charcot-Marie-Tooth disease (CMT), traditionally refers to a group of genetic disorders in which neuropathy is the main or sole feature. Its prevalence varies according to different populations s
Externí odkaz:
https://doaj.org/article/230c90fb55d04797baaac6f8f95671e7
Autor:
Antônio Gilson Prates Júnior, Fernando Augusto Medeiros Carrera Macedo, José Augusto Malheiros, Maria Letícia Marques Pinheiro, Lucas Rodrigues de Souza, Ana Luisa Ribeiro Pinto, Bruna Kelren Freitas Pohlmann
Publikováno v:
Brazilian Neurosurgery, Vol 42, Iss 04, Pp e348-e353 (2023)
Introduction Chagas disease is an important public health problem in Latin American countries, affecting ∼ 6 million people within the region. In patients with chronic Chagas disease who undergo some type of immunosuppression reactivation of the ac
Externí odkaz:
https://doaj.org/article/8ceaea9624d44aed891d21a4ea963c43
Publikováno v:
Gazeta Médica, Vol 1, Iss 1 (2023)
A asma é uma doença crónica muito frequente na infância, sendo o montelucaste utilizado no seu tratamento. Este fármaco tem sido associado a alterações neuropsiquiátricas potencialmente letais. O objetivo desta revisão é avaliar a evidênci
Externí odkaz:
https://doaj.org/article/cb99bdefdbd5443e80339527e9c09230
Autor:
Marcus Vinicius Pinto, Marcondes Cavalcante França, Marcus Vinicius Magno Gonçalves, Marcela Câmara Machado-Costa, Marcos Raimundo Gomes de Freitas, Francisco de Assis Aquino Gondim, Carlo Domenico Marrone, Alberto Rolim Muro Martinez, Carolina Lavigne Moreira, Osvaldo J. M. Nascimento, Anna Paula Paranhos Covaleski, Acary Souza Bulle de Oliveira, Camila Castelo Branco Pupe, Marcia Maria Jardim Rodrigues, Francisco Tellechea Rotta, Rosana Herminia Scola, Wilson Marques, Márcia Waddington-Cruz
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 03, Pp 308-321 (2023)
Hereditary transthyretin amyloidosis with peripheral neuropathy (ATTRv-PN) is an autosomal dominant inherited sensorimotor and autonomic polyneuropathy with over 130 pathogenic variants identified in the TTR gene. Hereditary transthyretin amyloidosis
Externí odkaz:
https://doaj.org/article/6b432dc2341e4394aae69773f46a71f4
Autor:
André Luiz Guimarães de Queiroz, Herval Ribeiro Soares Neto, Thiago Taya Kobayashi, Sonia Maria Cesar de Azevedo Silva
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 03, Pp 296-307 (2023)
Plasma exchange (PLEX) is a therapeutic apheresis modality in which the plasma is separated from inflammatory factors such as circulating autoreactive immunoglobulins, the complement system, and cytokines, and its therapeutic effect is based on the r
Externí odkaz:
https://doaj.org/article/ba91d22af86e43f98d29bf5481ddb384
Publikováno v:
Acta Médica Portuguesa, Vol 36, Iss 9 (2023)
A doença de Behçet é uma síndrome inflamatória multissistémica recidivante, caraterizada por úlceras orais e/ou genitais recorrentes, uveítes, artrite, lesões cutâneas e envolvimento gastrointestinal e neurológico. O neuro-Behçet correspo
Externí odkaz:
https://doaj.org/article/ba3727a9a44c4b17bbec9f0144c02643
Autor:
Jamilly da Silva Aragão, Inacia Sátiro Xavier de França, Rosilene Santos Baptista, Francisco Stélio de Sousa, Alexsandro Silva Coura, Ednário Barbosa de Mendonça
Publikováno v:
Aquichan, Vol 23, Iss 3 (2023)
Introdução: algumas pessoas, após lesão neurológica adquirida, estão em situações de maior vulnerabilidade a complicações, comorbidades e outras condições após a deficiência, as quais podem impactar na vida e na saúde, comprometer a qu
Externí odkaz:
https://doaj.org/article/9cf2065cc2554364be7cdec39f2af44b