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3. Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: report of three new mutations. Bachrach BE; Weinstein DA; Orho-Melander M; Burgess A; Wolfsdorf JI J Pediatr; 2002 Jun; 140(6):781-3. PubMed ID: 12072888 [TBL] [Abstract][Full Text] [Related]
4. [Hepatic glycogen synthetase deficiency or glycogen storage disease-zero. Mild phenotype with partial enzymatic defect]. de Kremer RD; de Capra AP; de Boldini CD; Hliba E; Givogri I Medicina (B Aires); 1990; 50(4):299-309. PubMed ID: 2130223 [TBL] [Abstract][Full Text] [Related]
5. Case report: liver glycogen synthase deficiency--a cause of ketotic hypoglycemia. Rutledge SL; Atchison J; Bosshard NU; Steinmann B Pediatrics; 2001 Aug; 108(2):495-7. PubMed ID: 11483824 [TBL] [Abstract][Full Text] [Related]
6. Low level of fasting plasma mannose in a child with glycogen storage disease type 0 (liver glycogen synthase deficiency). Miwa I; Taguchi T; Asano H; Murata T; Yorifuji T; Nagasaka H; Takatani T Clin Chim Acta; 2010 Jul; 411(13-14):998-9. PubMed ID: 20331987 [No Abstract] [Full Text] [Related]
13. Ketotic hypoglycemia. Catlett JP W V Med J; 1983 Jun; 79(6):126-8. PubMed ID: 6412460 [No Abstract] [Full Text] [Related]
14. [Hepatic glycogenosis without known enzyme deficiency with clinical and biological signs of type I Cori disease]. Badoual J; Lestradet H; Tichet J; Sanna N; Grenet P Ann Pediatr (Paris); 1972; 19(6):507-14. PubMed ID: 4341584 [No Abstract] [Full Text] [Related]
15. Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia. Hacıhamdioğlu B; Özgürhan G; Çaran B; Meydan-Aksanlı E; Keskin E Turk J Pediatr; 2018; 60(5):581-583. PubMed ID: 30968641 [TBL] [Abstract][Full Text] [Related]
16. [A case of glycogenosis with recurrent hypoglycemia without enzymatic deficiency on liver biopsy]. Grenet P; Badoual J; Lestradet H; Martinetti J; Sanna N; Voyer J Ann Pediatr (Paris); 1972; 19(6):499-506. PubMed ID: 4341583 [No Abstract] [Full Text] [Related]
17. [Case of diagnostics of a rare form of glycogen disease]. Atanesyan RA; Vorontsova MV; Vdovina TM; Klimov LY; Andreeva EI; Saneeva GA; Arakelyan RI Probl Endokrinol (Mosk); 2020 Nov; 66(5):79-85. PubMed ID: 33369375 [TBL] [Abstract][Full Text] [Related]