Search
Now showing items 1-10 of 754
Insuficiência cardíaca congestiva na distrofia muscular de Duchenne: um relato de caso
(HCPA/FAMED/UFRGS, 2012)
Citocinas inflamatórias na distrofia muscular de duchenne: uma revisão de literatura
(Universidade Federal do Rio Grande do NorteBrasilUFRNNutrição, 2021)
The value of dog for knowledge of human Duchenne muscular dystrophy: New findings in pathogenesis and therapeutic advances
(2015-04-01)
Duchenne muscular dystrophy (DMD) is the most devastating form of inherited muscular dystrophy in men. The loss of dystrophin causes progressive weakness and degeneration of skeletal and cardiac muscle leading to the ...
Transaminases increase: A manifestation of Duchenne's muscular dystrophy Aumento de transaminasas: Una manifestación de distrofia muscular de Duchenne
(2012)
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminases are produced in various body tissues, including striated muscle, so their blood elevation is not due exclusively to ...
Survival of patients with duchenne muscular dystrophy Sobrevida de pacientes con distrofia muscular de duchenne
(Sociedad Chilena de Pediatria, 2018)
© 2018, Sociedad Chilena de Pediatria. All rights reserved. Introduction: Duchenne muscular dystrophy (DMD) leads to a progressive deterioration of the muscle function and premature death. There are no longitudinal studies ...
Perfil comportamental e competência social de crianças e adolescentes com distrofia muscular de DuchenneBehavior profile and social competence in children and adolescents with Duchenne muscular dystrophy
(PPgPsi-UFRN, 2012)
A distrofia muscular de Duchenne é uma doença genética caracterizada por enfraquecimento muscular progressivo e degeneração irreversível, acompanhados por danos sensoriais e neuropsicológicos. Os objetivos do estudo ...
Enhanced urinary spontaneous luminescence in duchenne muscular dystrophy
(1994)
Urinary spontaneous visible luminescence is enhanced in children with Duchenne Muscular Dystrophy (DMD). This result is indicative of systemic oxidative stress in DMD patients. It is proposed that measurement of the urinary ...
Cell surface and gene expression regulation molecules in dystrophinopathy: mdx vs. Duchenne
(Sociedad de Biología de Chile, 2005)
Evolução do estado nutricional de pacientes com Distrofia Muscular de DuchenneEvolution of nutritional status of patients with Duchenne Muscular Dystrophy
(Universidade Federal do Rio Grande do NorteBrasilUFRNNutrição, 2018)
Caracterização clínica do sistema estomatognático na distrofia muscular de Duchenne: descrição de série de casos
(Instituto de Ciência da SaúdeICSBrasil, 2018-07-16)
A distrofia muscular de Duchenne (DMD) é uma doença neuromuscular hereditária
progressiva, de herança recessiva ligada ao cromossomo X. As manifestações clínicas se iniciam
na infância com enfraquecimento muscular ...