Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Marcos Raimundo Gomes de Freitas"'
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
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 79, Iss 6, Pp 554-556 (2021)
ABSTRACT The Paraguayan War ended 150 years ago. Back then, there were outbreaks of combatants’ limb weakness and tingling related to "palustrian cachexia", not clearly funded at the time on nutritional deficiency, the use of native flora to feed t
Externí odkaz:
https://doaj.org/article/7d74ef04275d4163936604c691b5c0f0
Autor:
Marco Orsini, Agnaldo José Lopes, Sara Lucia Silveira de Menezes, Acary Bulle Oliveira, Marcos Raimundo Gomes de Freitas, Osvaldo Jose Moreira do Nascimento, Fernando Silva Guimarães
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 73, Iss 10, Pp 873-876 (2015)
Amyotrophic lateral sclerosis is a progressive neuromuscular disease, resulting in respiratory muscle weakness, reduced pulmonary volumes, ineffective cough, secretion retention, and respiratory failure. Measures as vital capacity, maximal inspirator
Externí odkaz:
https://doaj.org/article/37424ca67c944a238e71b967b596799f
Autor:
Rouse Barbosa Pereira, Lílian Ramiro Felício, Arthur de Sá Ferreira, Sara Lúcia de Menezes, Marcos Raimundo Gomes de Freitas, Marco Orsini
Publikováno v:
Fisioterapia e Pesquisa, Vol 21, Iss 1, Pp 87-93 (2014)
The Charcot-Marie-Tooth (CMT) disease is a peripheral hereditary neuropathy with progressive distal muscle atrophy and weakness, mainly in lower limbs, that evolves limiting the gait and balance. The objective of the study was to analyse the immediat
Externí odkaz:
https://doaj.org/article/981748e5d8ca4012855a549e75863570
Autor:
Cristiane Nascimento Soares, Mauro Cabral-Castro, Celina Oliveira, Luis Claudio Faria, José Mauro Peralta, Marcos Raimundo Gomes de Freitas, Marzia Puccioni-Sohler
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 66, Iss 2a, Pp 234-237 (2008)
BACKGROUND: Dengue infection may cause neurological manifestations such as encephalitis, myelitis, mononeuropathies, acute disseminated encephalomyelitis, and Guillain Barré syndrome (GBS). In endemic regions, the infection course can be oligosympto
Externí odkaz:
https://doaj.org/article/9385dfaf66bb43b1aeda9c93c28f4982
Autor:
Ursula Thomé, Alexandre Fernandes, Osvaldo José Moreira do Nascimento, Marcos Raimundo Gomes de Freitas, Marco Antônio Araujo Leite
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 68, Iss 3, Pp 466-468 (2010)
Externí odkaz:
https://doaj.org/article/2d68d0f2e3e64a918d4121e54b286563
Autor:
Marcus Vinicius Pinto, Amilton Antunes Barreira, Acary Souza Bulle, Marcos Raimundo Gomes de Freitas, Marcondes Cavalcante França Jr, Francisco de Assis Aquino Gondim, Carlo Domenico Marrone, Wilson Marques Jr, Osvaldo J. M. Nascimento, Francisco Tellechea Rotta, Camila Pupe, Márcia Waddington-Cruz
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 76, Iss 9, Pp 609-621
ABSTRACT Transthyretin familial amyloid polyneuropathy is an autosomal dominant inherited sensorimotor and autonomic polyneuropathy, which if untreated, leads to death in approximately 10 years. In Brazil, liver transplant and tafamidis are the only
Externí odkaz:
https://doaj.org/article/bac3cbd3582e468fb19be0762863d1ce
Autor:
Francisco de Assis Aquino Gondim, Amilton Antunes Barreira, Rinaldo Claudino, Márcia Waddington Cruz, Francisco Marcos Bezerra da Cunha, Marcos Raimundo Gomes de Freitas, Marcondes Cavalcante França Jr, Marcus Vinícius Magno Gonçalves, Wilson Marques Jr, Osvaldo José Moreira Nascimento, Acary Souza Bulle Oliveira, Raquel Campos Pereira, Camila Pupe, Francisco Tellechea Rotta, Pedro Schestatsky
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 76, Iss 3, Pp 200-208
ABSTRACT The aim of this study was to describe the results of a Brazilian Consensus on Small Fiber Neuropathy (SFN). Fifteen neurologists (members of the Brazilian Academy of Neurology) reviewed a preliminary draft. Eleven panelists got together in t
Externí odkaz:
https://doaj.org/article/0a092ced33d34a21ba2724601ed6caa7
Autor:
Renato Puccioni SOHLER, Leonã Santana DE LIMA, Vinícius Zanotti ZATTA, Claude Jacques CHAMBRIARD, Marcos Raimundo Gomes DE FREITAS
Publikováno v:
Arquivos de Neuro-Psiquiatria
ABSTRACT Background: The famous Brazilian Baroque sculptor named Antônio Francisco Lisboa, known as “Aleijadinho” (1738–1814), suffered from a deforming disease of the lower and upper limbs. The condition was characterized by atrophy, paresis
Externí odkaz:
https://doaj.org/article/846c5200c07742a19932a298b38cddb0
Autor:
Alexandre Marins Rocha, Suzane Garcia Ferreira, Marcelo Souto Nacif, Mario Luiz Ribeiro, Marcos Raimundo Gomes de Freitas, Cláudio Tinoco Mesquita
Publikováno v:
Arquivos Brasileiros de Cardiologia, Iss 0
Abstract Background: Amyloidosis is a disease caused by deposits of insoluble fibrils in extracellular spaces. The most common type of familial amyloidosis is mediated by mutation of transthyretin, especially Val30Met. Symptoms and ejection fraction
Externí odkaz:
https://doaj.org/article/1b6c31696f3d4e11b230d5415e73b16c