Buscar
Mostrando ítems 1-10 de 199
Non-myogenic tumors display altered expression of dystrophin (DMD) and a high frequency of genetic alterations
(Impact Journals LLC, 2017-01)
DMD gene mutations have been associated with the development of Dystrophinopathies. Interestingly, it has been recently reported that DMD is involved in the development and progression of myogenic tumors, assigning DMD a ...
Human adipose tissue derived pericytes increase life span in Utrn tm1Ked Dmd mdx /J Mice
(SpringerTotowa, 2014-06-19)
Duchenne muscular dystrophy (DMD) is still an untreatable lethal X-linked disorder, which affects 1 in 3500 male births. It is caused by the absence of muscle dystrophin due to mutations in the dystrophin gene. The potential ...
Influence of different types of corticosteroids on heart rate variability of individuals with duchenne muscular dystrophy—a pilot cross sectional study
(2021-08-01)
Individuals with Duchenne Muscular Dystrophy (DMD) have an impairment of cardiac autonomic function categorized by parasympathetic reduction and sympathetic predominance. The objective of this study was to assess the cardiac ...
Autonomic modulation in duchenne muscular dystrophy during a computer task: A prospective control trial
(2017-01-01)
Introduction: Duchenne Muscular Dystrophy (DMD) is characterized by progressive muscle weakness that can lead to disability. Owing to functional difficulties faced by individuals with DMD, the use of assistive technology ...
Family-based genome-wide association study in Patagonia confirms the association of the DMD locus and cleft lip and palate
(Wiley Blackwell Publishing, Inc, 2015-10)
The etiology of cleft lip with or without cleft palate (CL±P) is complex and heterogeneous, and multiple genetic and environmental factors are involved. Some candidate genes reported to be associated with oral clefts are ...
Visuospatial attention disturbance in Duchenne muscular dystrophy
(WILEY-BLACKWELL PUBLISHING, INC, 2010)
AIM The cognitive deficits present in the Duchenne muscular dystrophy (DMD) are not yet well characterized. Attention, considered to be the brain mechanism responsible for the selection of sensory stimuli, could be disturbed ...
Padronização de parâmetros eletrocardiográficos de cães da raça Golden Retriever clinicamente sadios
(RIO DE JANEIRO, 2010)
A distrofia muscular de Duchenne (DMD) em humanos é uma alteração neuromuscular hereditária, de caráter recessivo, ligada ao cromossomo X e causada pela ausência ou disfunção da distrofina. Clinicamente, caracteriza-se por ...
OPTIMIZATION OF WATER REMOVAL IN THE PRESS SECTION OF A PAPER MACHINE
(Brazilian Soc Chemical EngSao PauloBrasil, 2010)
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 ...