{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T10:23:12Z","timestamp":1760782992416},"reference-count":12,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[1991,1,1]],"date-time":"1991-01-01T00:00:00Z","timestamp":662688000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pathology"],"published-print":{"date-parts":[[1991]]},"DOI":"10.3109\/00313029109061442","type":"journal-article","created":{"date-parts":[[2007,11,20]],"date-time":"2007-11-20T01:24:50Z","timestamp":1195521890000},"page":"62-65","source":"Crossref","is-referenced-by-count":7,"title":["Peripheral nerve and vasculature involvement in myophosphorylase deficiency (mcardle\u2019s disease)"],"prefix":"10.1016","volume":"23","author":[{"given":"Roger W.","family":"Byard","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Boleslaw","family":"Lach","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David N.","family":"Preston","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.3109\/00313029109061442_bib0005","doi-asserted-by":"crossref","first-page":"635","DOI":"10.1002\/ajmg.1320250406","article-title":"Metabolic myopathies","volume":"25","author":"DiMauro","year":"1986","journal-title":"Am J Med Genet"},{"key":"10.3109\/00313029109061442_bib0010","series-title":"Myology","first-page":"1585","article-title":"Phosphorylase deficiency","author":"DiMauro","year":"1986"},{"key":"10.3109\/00313029109061442_bib0015","doi-asserted-by":"crossref","first-page":"236","DOI":"10.1111\/j.1699-0463.1967.tb01286.x","article-title":"An improved method for the histochemical demonstration of phosphorylase in tissue sections","volume":"70","author":"Korsgaard","year":"1967","journal-title":"Acta Pathol Microbiol Scand"},{"key":"10.3109\/00313029109061442_bib0020","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1001\/archneur.1970.00480190012002","article-title":"Histochemical diagnosis of muscle phosphofructokinase deficiency","volume":"22","author":"Bonilla","year":"1970","journal-title":"Arch Neurol"},{"key":"10.3109\/00313029109061442_bib0025","doi-asserted-by":"crossref","first-page":"422","DOI":"10.1002\/ana.410050504","article-title":"Debrancher deficiency: Neuromuscular disorder in five adults","volume":"5","author":"DiMauro","year":"1978","journal-title":"Ann Neurol"},{"key":"10.3109\/00313029109061442_bib0030","doi-asserted-by":"crossref","first-page":"1558","DOI":"10.1212\/WNL.37.9.1558","article-title":"McArdle\u2019s disease in two generations: Autosomal recessive transmission with manifesting heterozygote","volume":"37","author":"Schmidt","year":"1987","journal-title":"Neurology"},{"key":"10.3109\/00313029109061442_bib0035","doi-asserted-by":"crossref","first-page":"272","DOI":"10.1002\/mus.880100311","article-title":"The pattern of involvement of adult-onset acid maltase deficiency at autopsy","volume":"10","author":"Van der Walt","year":"1987","journal-title":"Muscle Nerve"},{"key":"10.3109\/00313029109061442_bib0040","doi-asserted-by":"crossref","first-page":"294","DOI":"10.1002\/ana.410190313","article-title":"Accumulation of glycogen in sural nerve axons in adult-onset Type III glycogenosis","volume":"19","author":"Ugawa","year":"1986","journal-title":"Ann Neurol"},{"key":"10.3109\/00313029109061442_bib0045","doi-asserted-by":"crossref","first-page":"300","DOI":"10.1007\/BF00687012","article-title":"Intra-axonal polysaccharide deposits in the peripheral nerve seen in adult polysaccharide storage myopathy","volume":"65","author":"Komure","year":"1985","journal-title":"Acta Neuropathol (Berl)"},{"key":"10.3109\/00313029109061442_bib0050","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1016\/0022-510X(87)90078-5","article-title":"Absence of biochemical heterogeneity in McArdle\u2019s diseases. A high resolution SDS-polyacrylamide gel electrophoresis study","volume":"78","author":"Mantle","year":"1987","journal-title":"J Neurol Sci"},{"key":"10.3109\/00313029109061442_bib0055","series-title":"Disorders of Voluntary Muscle","first-page":"298","article-title":"Ultrastructural studies ol diseased muscle","author":"Mastaglia","year":"1981"},{"key":"10.3109\/00313029109061442_bib0060","doi-asserted-by":"crossref","first-page":"559","DOI":"10.3109\/01913128009140562","article-title":"Overview Article: Basal lamina of epidermis, muscle fibres, muscle capillaries, and renal tubules: Changes with ageing and in diabetes mellitus","volume":"1","author":"Vracko","year":"1980","journal-title":"Ultrastruct Pathol"}],"container-title":["Pathology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0031302516361542?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0031302516361542?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,1,2]],"date-time":"2019-01-02T23:00:58Z","timestamp":1546470058000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0031302516361542"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1991]]},"references-count":12,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1991]]}},"alternative-id":["S0031302516361542"],"URL":"https:\/\/doi.org\/10.3109\/00313029109061442","relation":{},"ISSN":["0031-3025"],"issn-type":[{"value":"0031-3025","type":"print"}],"subject":[],"published":{"date-parts":[[1991]]}}}