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Evaluation of intracellular calcium in golden retriever muscular dystrophy
(2011-07-01)
The present study had the objective of evaluating calcium accumulations in muscle fibers and their correlation with the canine muscular dystrophy. After the deaths of the animals (13 dystrophic and 3 non-dystrophic), samples ...
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 ...
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 ...
LONG-TERM THERAPY WITH DEFLAZACORT DECREASES MYOCARDIAL FIBROSIS IN mdx MICE
(John Wiley & Sons IncHobokenEUA, 2009)
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 ...