Myophosphorylase deficiency (McArdle's disease) in two interrelated families-Reference-Cited by-同舟云学术

Myophosphorylase deficiency (McArdle's disease) in two interrelated families

Published:1973-04-01 Issue:2 Volume:36 Page:217-224
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:Journal of Neurology, Neurosurgery & Psychiatry

Author:

Cochrane P.,Hughes R. R.,Buxton P. H.,Yorke R. A.

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference21 articles.

1. Histopathology of McArdle's disease in a family;Bale, P.; Hammett, J.F.; Neale, F.C.;Journal of Pathology and Bacteriology,1967

2. The colorimetric determination of lactic acid in biological material;Barker, S.B.; Summerson, W.H.;Journal of Biological Chemistry,1941

3. Fenfluramine and muscle glucose uptake in man;Butterfield, W.J.H.; Whichelow, M.J.;Lancet,1968

4. An electromyographic diagnostic screening test in McArdle's disease and a case report;Dyken, M.L.; Smith, D.M.; Peake, R.L.;Neurology (Minneapolis),1967

5. A case of McArdle's syndrome with a positive family history;Hockaday, T.D.R.; Downey, J.A.; Mottram, R.F.;Journal of Neurology, Neurosurgery, and Psychiatry,1964

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