Next »
Journal of the Neurological Sciences
Volume 201, Issue 1
, Pages 27-31
, 15 September 2002
“Cap disease”—a failure in the correct muscle fibre formation
References
- . “Cap disease” new congenital myopathy. Neurology. 1981;31:1113–1120
-
.
Cap disease myopathy: a rare type of congenital myopathy.
Neuromuscul. Disord. 1996;(Suppl. 559):
- . Human ontogenesis: I. Ultrastructural characteristics of developing human muscle. J. Neuropathol. Exp. Neurol. 1980;39:476–486
-
.
An approach to the pathogenesis of some congenital myopathies.
In:
Dimitrijevic MR, et al. editor. Progressive neuromuscular diseases.
Recent Achievements in Restorative Neurology. vol. 2:Krager; 1986;p. 305–317
- . The fusion of myoblast. Biochem. J. 1985;228:1–12
- . Transcriptional regulation of decreased protein synthesis during skeletal muscle unloading. J. Appl. Physiol. 1989;66:1093–1098
-
.
Myosin heavy-chain composition in striated muscle after tenotomy.
Biochem. J. 1992;282:237–242
-
.
Myosin heavy chains in striated muscle after immobilization.
BAM. 1992;2:97–106
-
.
Myosin heavy chains in striated muscle immobilized in a shortened position.
BAM. 1995;5:147–153
PII: S0022-510X(02)00156-9
© 2002 Elsevier Science B.V. All rights reserved.
Next »
Journal of the Neurological Sciences
Volume 201, Issue 1
, Pages 27-31
, 15 September 2002
