The mother in family 5 had a brother with Duchenne muscular dystrophy.

This difference is considered an important clue to possible future treatment of Duchenne muscular dystrophy.

He is also credited with the discovery of Duchenne muscular dystrophy.

A maverick researcher says he has developed the first effective treatment for Duchenne muscular dystrophy.

Duchenne muscular dystrophy afflicts about one in every 3,500 live male births.

Duchenne muscular dystrophy, the most common form of the disease, strikes males almost exclusively.

An evaluation of some carrier detection techniques in Duchenne muscular dystrophy.

Electrocardiographic studies in the patients of Duchenne muscular dystrophy.

Until now, no treatment was available for Duchenne muscular dystrophy, the severest and most common childhood form of the disease.

The relevance of this variant protein to Duchenne muscular dystrophy is not known.

Becker is a milder form of Duchenne muscular dystrophy.

To assess the acceptability of screening newborn boys for Duchenne muscular dystrophy.

In it, the actor was cast as the principal character: a maverick with duchenne muscular dystrophy.

Their older brother was dying of Duchenne muscular dystrophy, a genetic disease that destroys its victims slowly.

When given to 19 children with Duchenne muscular dystrophy, researchers found that higher doses of the drug led to an increase in dystrophin.

Duchenne muscular dystrophy can be detected with about 95% accuracy by genetic studies performed during pregnancy.

Bhati suffers from Duchenne muscular dystrophy and is confined to a wheelchair.

In the case of Duchenne muscular dystrophy, the protein that becomes compromised is dystrophin.

Duchenne muscular dystrophy, which is associated with mutations in the dystrophin gene.

This confirmed Duchenne muscular dystrophy in each case (table II).

Carnitine metabolism in early stages of Duchenne muscular dystrophy.

Soon afterwards, Alfredo fell ill, suffering from Duchenne muscular dystrophy.

In Duchenne muscular dystrophy, the genetic mutation is out-of-frame.

A recent study has identified osteopontin as a determinant of disease severity in patients with Duchenne muscular dystrophy.

Waitzkin is active in the fight against Duchenne Muscular Dystrophy.