{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T04:26:54Z","timestamp":1777868814823,"version":"3.51.4"},"reference-count":0,"publisher":"S. Karger AG","license":[{"start":{"date-parts":[[2017,8,11]],"date-time":"2017-08-11T00:00:00Z","timestamp":1502409600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/karger.com\/pages\/terms-and-conditions"},{"start":{"date-parts":[[2017,8,11]],"date-time":"2017-08-11T00:00:00Z","timestamp":1502409600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/karger.com\/pages\/terms-and-conditions"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Enzyme"],"abstract":"<jats:p>Studies have been conducted on\nthree types of glycogen storage diseases: (1) the\nmolecular heterogeneity of muscle phosphorylase\ndeficiency (type V) has been shown by demonstration\nof the presence of cross-reacting immunological\nmaterial in one out of two cases; (2) the presence\nof cross-reacting material has been demonstrated in 18 tissue samples from patients\nwith amylo-1,6-glucosidase deficiency (type III); (3) the existence of pathological\nvariants of amylo-1,4-glucosidase (type II) has been shown by electrophoresis\nand thermal denaturation. In addition, the molecular distinction between \u2018neutral\u2019\nand \u2018acid\u2019 amyloglucosidase has been provided using electrophoretic and immunological\ntechniques.<\/jats:p>","DOI":"10.1159\/000459414","type":"journal-article","created":{"date-parts":[[2017,8,11]],"date-time":"2017-08-11T17:12:52Z","timestamp":1502471572000},"page":"60-72","source":"Crossref","is-referenced-by-count":6,"title":["Molecular Studies on Glycogen Storage Diseases"],"prefix":"10.1159","author":[{"given":"Jean-Claude","family":"Dreyfus","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dominique","family":"Proux","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yvonne","family":"Alexandre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"127","published-online":{"date-parts":[[2017,8,11]]},"container-title":["Enzyme"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/karger.com\/article-pdf\/doi\/10.1159\/000459414","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,30]],"date-time":"2026-04-30T12:43:59Z","timestamp":1777553039000},"score":1,"resource":{"primary":{"URL":"https:\/\/karger.com\/article\/doi\/10.1159\/000459414"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,8,11]]},"references-count":0,"URL":"https:\/\/doi.org\/10.1159\/000459414","archive":["Portico"],"relation":{},"ISSN":["0013-9432","2504-2564"],"issn-type":[{"value":"0013-9432","type":"print"},{"value":"2504-2564","type":"electronic"}],"subject":[],"published":{"date-parts":[[2017,8,11]]}}}