Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Mario Emilio Dourado"'
Autor:
Pedro Henrique Almeida Fraiman, Mariana Freire, Bruno Fernandes, Felipe Palitot, Nathalia Mota, Eduardo Sequerra, Glauco Santos, Mario Emilio Dourado, Clecio de Oliveira Godeiro-Junior, Manuel Moreira-Neto
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 01, Pp 001-006 (2024)
Background Chikungunya is a mosquito-borne disease caused by the chikungunya virus (CHIKV) and can lead to neurological complications in severe cases.
Externí odkaz:
https://doaj.org/article/27d7ab982de742579d3ff26f39c7b0a1
Autor:
Vanessa R Resqueti, Guilherme A F Fregonezi, Karen Pondofe, Ozana Brito, Mario Emilio Dourado Júnior, Rodrigo Torres-Castro
Publikováno v:
BMJ Open, Vol 11, Iss 4 (2021)
Introduction This study aims to investigate the effects of an optimal home-based respiratory care protocol in individuals with amyotrophic lateral sclerosis (ALS).Methods and analysis This is a randomised, blinded controlled trial involving patients
Externí odkaz:
https://doaj.org/article/d8dfd06368ec405d8950b7431dc47106
Autor:
Guilherme Fregonezi, Palomma Russelly Saldanha Araújo, Tathiana Lindemberg Ferreira Macêdo, Mario Emilio Dourado Junior, Vanessa Regiane Resqueti, Armele de Fátima Dornelas de Andrade
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 3, Pp 146-152 (2013)
ObjectiveIt was study the relationship between respiratory muscle strength and forced vital capacity (FVC) in patients with amyotrophic lateral sclerosis (ALS) versus healthy subjects.MethodsPulmonary function and respiratory muscle strength [maximal
Externí odkaz:
https://doaj.org/article/2cf12174a8644e9db4a69752edb174cf
Autor:
Guilherme Fregonezi, Palomma Russelly Saldanha Araújo, Tathiana Lindemberg Ferreira Macêdo, Mario Emilio Dourado Junior, Vanessa Regiane Resqueti, Armele de Fátima Dornelas de Andrade
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 3, Pp 146-152 (2013)
Objective It was study the relationship between respiratory muscle strength and forced vital capacity (FVC) in patients with amyotrophic lateral sclerosis (ALS) versus healthy subjects. Methods Pulmonary function and respiratory m
Externí odkaz:
https://doaj.org/article/195592a879e443af956a452adfa18dbd
Autor:
Guilherme Fregonezi, Thaise Araújo, Mario Emilio Dourado Junior, Joceline Ferezini, Ester Silva, Vanessa Resqueti
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 98, Iss 4, Pp 353-361 (2012)
FUNDAMENTO: O envolvimento cardíaco é comum em pacientes com Distrofia Miotônica (DM). A Variabilidade da Frequência Cardíaca (VFC) é uma técnica simples e confiável que pode ser útil para estudar a influência do sistema nervoso autonômico
Externí odkaz:
https://doaj.org/article/1025b082277147c6ba241652e547c431
Autor:
Jaqueline Fernandes Pontes, Gardenia Maria Holanda Ferreira, Guilherme Fregonezi, Karine Cavalcanti Maurício de Sena-Evangelista, Mario Emilio Dourado Junior
Publikováno v:
Fisioterapia em Movimento, Vol 25, Iss 2, Pp 253-261
INTRODUÇÃO: As doenças neuromusculares infantis são crônicas, degenerativas e determinam alterações funcionais, musculares e nutricionais. OBJETIVOS: Avaliar sistematicamente a força muscular respiratória e o perfil postural e nutricional de
Externí odkaz:
https://doaj.org/article/7f95da10212743a1b1b880a73003f383
Autor:
Annemiek A. van der Eijk, Judith Drenthen, Wilson Marques, Laura de Koning, Suzanne C. Franken, Cintia Marchesoni, Nortina Shahrizaila, Selma M. B. Jeronimo, Manou R. Batstra, Samuel Arends, Sonja E. Leonhard, Mario-Emilio Dourado, Cheng-Yin Tan, Bart C. Jacobs, Ruth Huizinga, Ricardo R. Reisin, Andrea Sotelo, Belen Tillard, Dardo F. Casas, Luciana Leon Cejas
Publikováno v:
Journal of the Peripheral Nervous System, 26(4), 449-460. Wiley-Blackwell Publishing Ltd
Half of the world's population is at risk of arthropod-borne virus (arbovirus) infections. Several arbovirus infections have been associated with Guillain-Barré syndrome (GBS). We investigated whether arboviruses are driving GBS beyond epidemic phas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c3bd253197e4640ae5f1b2f5f7311b0
https://doi.org/10.1111/jns.12469
https://doi.org/10.1111/jns.12469
Autor:
Badrul Islam, Kathleen Bateman, Maria Lucia Brito Ferreira, Pieter A. van Doorn, Bart C. Jacobs, Susumu Kusunoki, Eppie M. Yiu, Hugh J. Willison, Ricardo Reisin, Nortina Shahrizaila, Thirugnanam Umapathi, Mario Emilio Dourado, Cristiane Soares, Melissa R Mandarakas, Yuzhong Wang, Francisco de Assis Aquino Gondim, David R. Cornblath, Richard A. C. Hughes, James J. Sejvar, Sonja E. Leonhard, Carlos A. Pardo
Publikováno v:
Revista Neurociências. 29:1-52
A síndrome de Guillain–Barré (SGB) é uma doença imunomediada rara, mas potencialmente fatal, dos nervos periféricos e das raízes nervosas, que é geralmente desencadeada por infecções. A incidência da SGB pode, portanto, aumentar durante s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f8a6b1d6ceab0b200ebf7cea9de63e9
https://doi.org/10.34024/rnc.2021.v29.11725
https://doi.org/10.34024/rnc.2021.v29.11725
Autor:
Badrul Islam, Thirugnanam Umapathi, Mario Emilio Dourado, Melissa R. Mandarakas, Pieter A. van Doorn, James J. Sejvar, Susumu Kusunoki, Carlos A. Pardo, Cristiane Soares, Hugh J. Willison, Ricardo Reisin, Eppie M. Yiu, Francisco de Assis Aquino Gondim, Sonja E. Leonhard, Nortina Shahrizaila, Bart C. Jacobs, Maria Lucia Brito Ferreira, Richard A. C. Hughes, Yuzhong Wang, David R. Cornblath, Kathleen Bateman
Publikováno v:
Nature Reviews. Neurology
Nature Reviews Neurology, 15(11), 671-683. Nature Publishing Group
Nature Reviews Neurology, 15(11), 671-683. Nature Publishing Group
Guillain–Barré syndrome (GBS) is a rare, but potentially fatal, immune-mediated disease of the peripheral nerves and nerve roots that is usually triggered by infections. The incidence of GBS can therefore increase during outbreaks of infectious di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb71617de0324bbdb7f0dc2e11743d2
http://europepmc.org/articles/PMC6821638
http://europepmc.org/articles/PMC6821638
Autor:
Afagh Alavi, Yalda Nilipour, Luca Bello, Jorge Alonso-Pérez, Shahriar Nafissi, Muhammad Umair, Lidia Gonzalez-Quereda, Mario Emilio Dourado, Chiara Marini-Bettolo, Chiara Panicucci, Xavier Suárez-Calvet, Gultekin Kutluk, Kinga Hadzsiev, Lucas Michielon de Augusto Isihi, Edmar Zanoteli, Jordi Díaz-Manera, Thomas O. Crawford, Muhammad Younus, Ana Töpf, Naz Kadem, Elena Pegorano, Juan José Vilchez, Claudio Bruno, Pia Gallano, Béla Melegh, Michela Guglieri, Nuria Muelas, Volker Straub
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Universitat Autònoma de Barcelona
Sarcoglycanopathies include four subtypes of autosomal recessive limb-girdle muscular dystrophies (LGMDR3, LGMDR4, LGMDR5 and LGMDR6) that are caused, respectively, by mutations in the SGCA, SGCB, SGCG and SGCD genes. Delta-sarcoglycanopathy (LGMDR6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73651a42bdeaee241f06acea9ddd79f9
https://ddd.uab.cat/record/258072
https://ddd.uab.cat/record/258072
