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Morphological Changes in the Myotendinous Junction of mdx Mice
(2021-10-17)
The myotendinous junction (MTJ) is the interface between muscle and tendon, and it is the main area of force transmission of the locomotor apparatus. Dystrophic processes promote pathological injury which affects the ...
Distrofia Muscular de Duchenne: análise eletrocardiográfica de 131 casos
(Universidade Federal de São Paulo (UNIFESP), 2011-02-22)
Fundamento: É conhecido o envolvimento cardíaco em pacientes com distrofia muscular de Duchenne (DMD). O eletrocardiograma (ECG) apresenta algumas alterações típicas na DMD, fato que o torna um exame útil no diagnóstico ...
ALTERED GENE EXPRESSION PATHWAYS IN DUCHENNE MUSCULAR DYSTROPHY
(INTECH, 2012)
Duchenne muscular dystrophy (DMD) is caused by the absence of functional dystrophin (Blake et al. 2002). Dystrophin is a cytoskeleton protein normally expressed in the inner face of the plasma membrane (Ahn and Kunkel ...
Cell surface and gene expression regulation molecules in dystrophinopathy: mdx vs. Duchenne
(SOCIEDAD BIOLGIA CHILE, 2005)
Duchenne muscular dystrophy (DMD) is secondary to loss-of-function mutations in the dystrophin gene. The causes underlying the progression of DMD, differential muscle involvement, and the discrepancies in phenotypes among ...
Aumento de transaminasas: una manifestación de distrofia muscular de Duchenne
(Sociedad Chilena de Pediatría, 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 ...
Symptomatic female carriers of Duchenne Muscular Dystrophy (DMD): genetic and clinical characterization
(Elsevier, 2014-01-15)
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease caused by mutations in the dystrophin gene and is characterized by muscle degeneration and death. DMD affects males; females being asymptomatic carriers ...