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Autonomic function in patients with Duchenne muscular dystrophy

โœ Scribed by Miki Inoue; Kazuhiro Mori; Yasunobu Hayabuchi; Katsunori Tatara; Shoji Kagami


Book ID
108972547
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
275 KB
Volume
51
Category
Article
ISSN
1328-8067

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๐Ÿ“œ SIMILAR VOLUMES


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Over 90% of patients with Duchenne muscular dystrophy develop a scoliosis when they become wheelchair bound. The scoliosis is progressive and is associated with deteriorating lung function. The purpose of this study was firstly to assess whether a standing regimen, in patients who had gone off their

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Motor neuron abnormalities have been implicated in the pathogenesis of Duchenne muscular dystrophy. Evidence concerning the effect of injury on motor neurons of human Duchenne muscular dystrophy (DMD) is lacking. We report a DMD patient having, in addition, an obstetric paresis on his left arm. EMG

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Duchenne muscular dystrophy (DMD) is a fatal disorder affecting approximately 1 in 3500 live born males, characterized by progressive muscle weakness. Several different strategies are being investigated in developing a cure for this disorder. Until a cure is found, therapeutic and supportive care is