Results 291 to 300 of about 86,962 (305)

Erythrocytes in Duchenne dystrophy [PDF]

open access: possibleNeurology, 1981
James B. Atkinson   +2 more
openaire   +2 more sources

Duchenne’s Muscular Dystrophy

2018
Duchenne’s muscular dystrophy (DMD) is a progressive X-linked recessive disorder that affects boys and female carriers. It is the most common dystrophy with onset in childhood in the United States. It is associated with severe, progressive proximal muscle weakening due to absence of dystrophin, which is found in skeletal and cardiac muscles This ...
Kirk Lalwani, Tori Sutherland
openaire   +1 more source

Backache in a Duchenne boy

Neuromuscular Disorders, 2007
Kinali, M.   +4 more
openaire   +4 more sources

Duchenne Muscular Dystrophy

2004
Duchenne muscular dystrophy (DMD) is a common inherited disease with a worldwide incidence of 1 in 3,500 male births. Recent molecular study on the DMD gene identified a 14-kb mRNA encoded by 79 exons distributed over 2.5 million bp of the X-chromosome. The protein named dystrophin contains 3,685 amino acids. Most of the genetic events (mutations) that
openaire   +2 more sources

Dystrophin and Duchenne dystrophy

Neuromuscular Disorders, 2015
Victor Dubowitz, Ronald D. Cohn
openaire   +3 more sources

DUCHENNE DE BOULOGNE

Australian and New Zealand Journal of Surgery, 1979
openaire   +3 more sources

Duchenne's Legacy

Orthopedics, 2004
openaire   +2 more sources

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