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Duchenne muscular dystrophy

โœ Scribed by G. A. Danieli; M. L. Mostacciuolo; G. Pilotto; C. Angelini; A. Bonfante


Publisher
Springer
Year
1980
Tongue
English
Weight
486 KB
Volume
54
Category
Article
ISSN
0340-6717

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๐Ÿ“œ SIMILAR VOLUMES


Duchenne muscular dystrophy
โœ G. A. Danieli; G. Barbujani ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› Springer ๐ŸŒ English โš– 536 KB

A segregation analysis on 135 Duchenne families from Venetia (Italy) suggests that the proportion of sporadic cases might be less than expected. Support for this view is also given by an analysis of a pooled sample including 284 additional sibships from comparable studies published previously. Sever

Duchenne muscular dystrophy
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By a general survey in the hopitals of northeast Italy, Duchenne cases have been located and identified over a 20-year period. In a more restricted area screening for Duchenne carriers has been carried out in affected families. This procedure made possible an exact estimate of the incidence rate, pr

Duchenne muscular dystrophy carriers
โœ K. Matsumura; I. Nakano; N. Fukuda; H. Ikehira; Y. Tateno; Y. Aoki ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› Springer ๐ŸŒ English โš– 398 KB
Reinnervation in duchenne muscular dystr
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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

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โœ Dr. Delores Danilowicz; Monica Rutkowski; Dong Myung; Dora Schievely ๐Ÿ“‚ Article ๐Ÿ“… 1980 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 514 KB