{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,21]],"date-time":"2023-10-21T14:06:44Z","timestamp":1697897204944},"reference-count":6,"publisher":"Oxford University Press (OUP)","issue":"617","license":[{"start":{"date-parts":[[1977,3,1]],"date-time":"1977-03-01T00:00:00Z","timestamp":226022400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1977,3,1]]},"abstract":"<jats:title>Summary<\/jats:title>\n               <jats:p>A case of McArdle's disease in a man is described in detail and a less complete study of his family is reported. This patient showed the classical features of McArdle's disease and the diagnosis was confirmed by muscle biopsy. Unlike other reported cases of this disorder, this case showed a normal rise in blood lactate levels on ischaemic exercise. This apparently paradoxical finding is discussed. It is suggested that a normal rise in the level of blood lactate on ischaemic exercise should not exclude myophosphorylase deficiency.<\/jats:p>","DOI":"10.1136\/pgmj.53.617.161","type":"journal-article","created":{"date-parts":[[2008,12,29]],"date-time":"2008-12-29T20:39:26Z","timestamp":1230583166000},"page":"161-164","source":"Crossref","is-referenced-by-count":9,"title":["Lactate production in McArdle's disease"],"prefix":"10.1093","volume":"53","author":[{"given":"A K","family":"Baksi","sequence":"first","affiliation":[{"name":"Liverpool Royal Infirmary, Regional Centre for Medical and Surgical Neurology , Liverpool, , Liverpool"},{"name":"Stoke Mandeville Hospital, Aylesbury, and Royal Southern Hospital , Liverpool, , Liverpool"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P H","family":"Buxton","sequence":"additional","affiliation":[{"name":"Regional Centre for Medical and Surgical Neurology , Liverpool, , Liverpool"},{"name":"Stoke Mandeville Hospital, Aylesbury, and Royal Southern Hospital , Liverpool, , Liverpool"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P","family":"Cochrane","sequence":"additional","affiliation":[{"name":"Stoke Mandeville Hospital, Aylesbury, and Royal Southern Hospital , Liverpool"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R R","family":"Hughes","sequence":"additional","affiliation":[{"name":"Royal Southern Hospital , Liverpool"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[1977,3,1]]},"reference":[{"key":"ref_1","first-page":"13","article-title":"Myopathy due to a defect in muscle glycogen breakdown","volume":"10","author":"McARDLE, B.","year":"1951","unstructured":"McARDLE, B. (1951) Myopathy due to a defect in muscle glycogen breakdown. Clinical Science, 10, 13.","journal-title":"Clinical Science"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"1045","DOI":"10.1016\/S0140-6736(62)92145-1","article-title":"McArdle's syndrome: Phosphorylase deficient myopathy","volume":"i,","author":"MELLICK, R.S.; MAHLER, R.F.; HUGHES, B.P.","year":"1962","unstructured":"MELLICK, R.S., MAHLER, R.F. & HUGHES, B.P. (1962) McArdle's syndrome: Phosphorylase deficient myopathy. Lancet, i, 1045.","journal-title":"Lancet"},{"key":"ref_3","first-page":"298","article-title":"Defect in muscle phosphorylase: a newly defined human disease","volume":"7","author":"PEARSON, C.M.; RIMMER, D.G.; MOMMAERTS, W.F.N.M.","year":"1959","unstructured":"PEARSON, C.M., RIMMER, D.G. & MOMMAERTS, W.F.N.M. (1959) Defect in muscle phosphorylase: a newly defined human disease. Clinical Research, 7, 298.","journal-title":"Clinical Research"},{"key":"ref_4","first-page":"2231","article-title":"Hereditary absence of muscle phosphorylase (McArdle's syndrome)","volume":"264","author":"SCHMID, R.; HAMMAKER, L.","year":"1961","unstructured":"SCHMID, R. & HAMMAKER, L. (1961) Hereditary absence of muscle phosphorylase (McArdle's syndrome). New England Journal of Medicine, 264, 2231.","journal-title":"New England Journal of Medicine"},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"2044","DOI":"10.1172\/JCI103983","article-title":"Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle","volume":"38","author":"SCHMID, R.; MAHLER, R.","year":"1959","unstructured":"SCHMID, R. & MAHLER, R. (1959) Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle. Journal of Clinical Investigation, 38, 2044.","journal-title":"Journal of Clinical Investigation"},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1177\/3.3.153","article-title":"Histochemical detection of phosphorylase in animal tissues","volume":"3","author":"TAKEUCH, T.; KURIATI, H.","year":"1955","unstructured":"TAKEUCH, T. & KURIATI, H. (1955) Histochemical detection of phosphorylase in animal tissues. Journal of Histochemistry and Cytochemistry, 3, 153.","journal-title":"Journal of Histochemistry and Cytochemistry"}],"container-title":["Postgraduate Medical Journal"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/academic.oup.com\/pmj\/article-pdf\/53\/617\/161\/50185378\/postgradmedj-53-161.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/academic.oup.com\/pmj\/article-pdf\/53\/617\/161\/50185378\/postgradmedj-53-161.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,8]],"date-time":"2023-05-08T07:05:38Z","timestamp":1683529538000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/pmj\/article\/53\/617\/161\/7038244"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1977,3,1]]},"references-count":6,"journal-issue":{"issue":"617","published-online":{"date-parts":[[1977,3,1]]},"published-print":{"date-parts":[[1977,3,1]]}},"URL":"https:\/\/doi.org\/10.1136\/pgmj.53.617.161","relation":{},"ISSN":["0032-5473","1469-0756"],"issn-type":[{"value":"0032-5473","type":"print"},{"value":"1469-0756","type":"electronic"}],"subject":[],"published-other":{"date-parts":[[1977,3]]},"published":{"date-parts":[[1977,3,1]]}}}