Benign congenital muscular dystrophy with autosomal dominant heredity: problems of classification-Reference-Cited by-同舟云学术

Benign congenital muscular dystrophy with autosomal dominant heredity: problems of classification

Published:1987-04 Issue:3 Volume:234 Page:146-151
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Schmalbruch H.,Kamieniecka Z.,Fuglsang-Frederiksen A.,Trojaborg W.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/BF00314133.pdf

Reference20 articles.

1. Arts WF, Bethlem J, Volkers WS (1978) Further investigations on benign myopathy with autosomal dominant inheritance. J Neurol 217:201?206

2. Bethlem J, Van Wijngaarden GK (1976) Benign myopathy, with autosomal dominant inheritance. Brain 99:91?100

3. Bischoff R (1979) Tissue cultures studies on the origin of myogenic cells during muscle regeneration in the rat. In: Mauro A (ed) Muscle regeneration. Raven Press, New York, pp 13?29

4. Buchthal F (1957) Electrophysiological signs of myopathy as related to muscle biopsy. Acta Neurol Scand 32:1?29

5. Buchthal F, Kamieniecka Z (1982) The diagnostic yield of quantified electromyography and quantified muscle biopsy in neuromuscular disorders. Muscle Nerve 5:265?280

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