Adult onset scapuloperoneal myopathy.

Author:

Thomas P K,Schott G D,Morgan-Hughes J A

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference12 articles.

1. Zur nosologischen Stellung des sogenannten;Seitz, D.,1957

2. Etude Clinique sLir iine Forme Hereditaire d'Atrophie Musculaire Progressive debuitantpar les Membres Inferieurs (Type Femoral avec Griffe des Orteils);Brossard, J.,1886

3. Caraceni, T., Negri, S., and Cornelio, F. (1972). A myelogenic case of scapulo-tibio-peroneal atrophy. In Strutcture and Function ofNormal and Diseased Muscle and Peripheral Nerve, pp. 261-263. Edited by I. Hausmanowa-Petrusewicz and H. Je,drzejowska. Polish Medical Publications: Warsaw.

4. Myopathies scapuloperonieres. A propos;Serratrice, G.; Roux, H.; Aquaron, R.; Gambarelli, D.; Baret, J.,1969

5. Scapuloperoneal dystrophy associated with neurogenic changes;Takahashi, K.; Nakamura, H.; Nakashima, R.;Journal of the Neurological Sciences,1974

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