Results 1 to 10 of about 107 (97)
Distrofina na diferenciação das distrofias de duchenne e becker estudo imuno-histoquímico comparado com o estádio clínico, enzimas séricas e biópsia muscular [PDF]
Arquivos De Neuro-Psiquiatria, 1990 Foram estudados 55 casos de distrofia muscular progressiva (34 Duchenne, 12 Duchenne com distrofina residual e 9 Becker), comparando idade, época de início e tempo de sintomas, graduação na escala de Vignos e Archibald, níveis de enzimas séricas e ...
Lineu Cesar Werneck, E Bonilla
exaly +5 more sources
Atypical reaction to anesthesia in Duchenne/Becker muscular dystrophy [PDF]
Brazilian Journal of Anesthesiology, 2018 Background and objectives: Duchenne/Becker muscular dystrophy affects skeletal muscles and leads to progressive muscle weakness and risk of atypical anesthetic reactions following exposure to succinylcholine or halogenated agents.
Helga Cristina Almeida da Silva +5 more
doaj +2 more sources
Arquivos de Neuro-Psiquiatria, 1995 The dystrophin distribution in the plasma muscle membrane using immunohystochemistry was studied in 22 children with congenital muscular dystrophy. The dystrophin was detected by immunofluorescence in muscle biopsy through a polyclonal antibody.
Lineu Cesar Werneck, Eduardo Bonilla
doaj +2 more sources
Arquivos de Neuro-Psiquiatria, 2007 Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are caused by mutations in the dystrophin gene. We studied 106 patients with a diagnosis of probable DMD/BMD by analyzing 20 exons of the dystrophin gene in their blood and, in some of
Aline Andrade Freund +5 more
doaj +1 more source
Arquivos de Neuro-Psiquiatria, 1992 To ascertain whether dystrophin immunohistochemistry could improve DMD/ BMD carrier detection, we analyzed 14 muscle biopsies from 13 DMD and one BMD probable and possible carriers.
Acary S. Bulle Oliveira +6 more
doaj +1 more source
Arquivos de Neuro-Psiquiatria, 1997 O camundongo mdx desenvolve distrofia muscular recessiva ligada ao cromossoma X (locus Xp21.1) e não expressa distrofina. Embora não apresente intensa fibrose do tecido muscular e acúmulo de tecido adiposo, é considerado o modelo animal mais adequado da ...
Sandra Lopes Seixas +3 more
doaj +1 more source
Revista Peruana de Medicina Experimental y Salud Pública, 2019 Las distrofias musculares de Duchenne/Becker son enfermedades raras que reciben poca atención en nuestro medio. El objetivo del presente estudio fue implementar la técnica de amplificación múltiple dependiente de ligación por sondas (MLPA) y demostrar ...
Francia DP Huaman-Dianderas +4 more
doaj +1 more source
Arquivos de Neuro-Psiquiatria, 2005 The Duchenne muscular systrophy (DMD) is a muscular dystrophy with cognitive impairment present in 20-30% of the cases. In the present study, in order to study the relationship between the alpha-dystroglycan (alpha-DG) immunostaining in skeletal muscle ...
Conceição Campanario da Silva Pereira +3 more
doaj +1 more source
Arquivos de Neuro-Psiquiatria, 1992 Foram estudados por análise estatística 194 parâmetros clínicos, laboratoriais, eletrofisiológicos, histoquímicos e imuno-histoquímicos de 112 casos de distrofia muscular de Duchenne (DMD) e de 26 casos de distrofia muscular de Becker (DMB).
Lineu C. Werneck +2 more
doaj +1 more source
Treinamento físico na distrofia muscular de becker associada à insuficiência cardíaca
Arquivos Brasileiros de Cardiologia, 2011 A distrofia muscular de Becker (DMB) integra as distrofinopatias que ocorrem devido a mutações genéticas que expressam a proteína distrofina no cromossomo X.
Jean Marcelo Roque +5 more
doaj +1 more source