{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,6]],"date-time":"2026-05-06T19:56:13Z","timestamp":1778097373065,"version":"3.51.4"},"reference-count":8,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[1990,7,1]],"date-time":"1990-07-01T00:00:00Z","timestamp":646790400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Inher Metab Disea"],"published-print":{"date-parts":[[1990,7]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>In this retrospective study from five centres, 139 patients over 10 years of age with glycogen storage disease types I, III, VI and IX are described. Almost half of the patients with glycogen storage disease type Ia had retarded growth and most had hyperlipidaemia. One\u2010third of the patients had adenomas, although none of these showed malignant transformations. With increasing age the growth, liver size and hyperlipidaemia of patients with glycogen storage disease type III improve. However, there was a high incidence of myopathy and cardiomyopathy. Patients with glycogen storage disease types VI and IX had a normal growth pattern after childhood. Hepatomegaly and hyperchole\u2010sterolaemia, however, were still present in half of the patients.<\/jats:p>","DOI":"10.1007\/bf01799498","type":"journal-article","created":{"date-parts":[[2005,6,21]],"date-time":"2005-06-21T14:02:35Z","timestamp":1119362555000},"page":"411-418","source":"Crossref","is-referenced-by-count":79,"title":["The long\u2010term outcome of patients with glycogen storage diseases"],"prefix":"10.1002","volume":"13","author":[{"given":"G. P. A.","family":"Smit","sequence":"first","affiliation":[{"name":"Department of Paediatrics University Hospital of the University of Groningen  Oostersingel 59 Groningen 9713 EZ The Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Fernandes","sequence":"additional","affiliation":[{"name":"Department of Paediatrics University Hospital of the University of Groningen  Oostersingel 59 Groningen 9713 EZ The Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J. V.","family":"Leonard","sequence":"additional","affiliation":[{"name":"Institute of Child Health  London UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E. E.","family":"Matthews","sequence":"additional","affiliation":[{"name":"Institute of Child Health  London UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S. W.","family":"Moses","sequence":"additional","affiliation":[{"name":"Department of Paediatrics Soroko Medical Centre  Beer Sheba Israel"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Odievre","sequence":"additional","affiliation":[{"name":"Service de P\u00e9diatrie H\u00f4pital Antoine Beclere Clamart  France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K.","family":"Ullrich","sequence":"additional","affiliation":[{"name":"Klinik f\u00fcr Kinderheilkunde Westf\u00e4lische Wilhelms\u2010Universit\u00e4t M\u00fcnster  FRG"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[1990,7]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1038\/ki.1989.133"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM198801073180102"},{"key":"e_1_2_1_4_1","first-page":"166","article-title":"Hepatic adenomata in type Ia glycogen storage disease","volume":"111","author":"Coire C. 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