- ►annals.org GM Talente, RA Coleman, C Alter, L Baker, BI … - Annals of internal medicine, 1994 - Am Coll Physicians Add to CiteULike Add to Complore Add to Connotea Add to Del.icio.us Add to Digg
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Objective: To identify complications amenable to prevention in adults with ... Cited by 107 - Related articles - BL Direct - All 3 versions
P Labrune, P Trioche, I Duvaltier, P Chevalier, … - Journal of pediatric gastroenterology and nutrition, 1997 - journals.lww.com Background: Hepatocellular adenomas may develop in patients with glycogen
storage disease types I and III, and the malignant degeneration of adenomas in
hepatocellular carcinoma has been reported in ten cases. The aim of this ... Cited by 94 - Related articles - BL Direct - All 3 versions
L Bianchi - European Journal of Pediatrics, 1993 - Springer Abstract. From 50 published cases of hepatocellular ade- noma (HCA) in glycogen
storage disease, type I (GSD I) some characteristic features may be deduced: 1.
The male: female ratio was 2:1. This sharply contrasts to HCA of other ... Cited by 75 - Related articles - BL Direct - All 2 versions
PJ Lee, DS Celermajer, J Robinson, SN … - Atherosclerosis, 1994 - ncbi.nlm.nih.gov Patients with glycogen storage disease type 1 (GSD-1) often have marked
hyperlipidaemia with abnormal lipoprotein profiles. This metabolic abnormality
improves, but is not fully corrected, with dietary therapy and therefore ... Cited by 30 - Related articles - All 3 versions
YT Chen, RA Coleman, JI Scheinman, PC … - New England Journal of Medicine, 1988 - content.nejm.org Although kidney enlargement occurs in Type I glycogen storage disease, renal
disease has not been considered a major problem. Death from renal failure in
three patients known to us prompted a study of renal function in this ... Cited by 109 - Related articles - All 4 versions
GPA Smit - European Journal of Pediatrics, 1993 - Springer Abstract. Forty-one patients (16 females and 25 males) over 10 years of age from
five different European centres were studied retrospectively. Of those patients
19 were below the 3rd percentile for height. Hypo- glycaemia was still ... Cited by 28 - Related articles - BL Direct - All 2 versions
P Parker, I Burr, A Slonim, FK Ghishan, H … - Gastroenterology, 1981 - ncbi.nlm.nih.gov Individuals with type Ia glycogen storage disease (glucose-6-phosphatase
deficiency) frequently develop hepatic adenomas. Potential complications
involving these adenomas include malignant transformation and hemorrhage. ... Cited by 49 - Related articles - All 3 versions
L Faivre, D Houssin, J Valayer, J Brouard, M … - Journal of inherited metabolic disease, 1999 - Springer Page 1. J. Inher. Metab. Dis. 22 723ยป732 (1999) SSIEM and Kluwer Academic
Publishers. Printed in the Netherlands ( Long-term outcome ... Cited by 42 - Related articles - BL Direct - All 6 versions
GPA Smit, J Fernandes, JV Leonard, EE … - Journal of Inherited Metabolic Disease, 1990 - Springer Summary: 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 ... Cited by 47 - Related articles - All 3 versions
- ►ufrgs.br [PDF] JP Rake, G Visser, P Labrune, JV Leonard, K … - European journal of pediatrics, 2002 - Springer Abstraet Glycogen storage disease type I (GSD I) is a relatively rare metabolic
disease and therefore, no meta- bolic centre has experience of large numbers of
patients. To document outcome, to develop guidelines about (long- term) ... Cited by 61 - Related articles - BL Direct - All 7 versions
