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2. Glycogen storage disease. (Report of three cases). Devi T; Mathew O Indian Pediatr; 1971 Jan; 8(1):43-5. PubMed ID: 5284580 [No Abstract] [Full Text] [Related]
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. [Glycogen storage disease, type VII. Muscular phosphofructokinase deficiency]. Tarui S Saishin Igaku; 1969 Jun; 24(6):1235-46. PubMed ID: 4241020 [No Abstract] [Full Text] [Related]
6. Report of the first family of glycogen storage disease among Egyptians. el Gholmy A; Hashem N; Khalifa AS; Osman N; Abdel Hamid G J Egypt Med Assoc; 1965; 48(2):130-41. PubMed ID: 5213078 [No Abstract] [Full Text] [Related]
12. Laboratory diagnosis of the neuromuscular glycogen storage diseases. Farmer PM Ann Clin Lab Sci; 1982; 12(6):431-8. PubMed ID: 6817693 [TBL] [Abstract][Full Text] [Related]
13. [Glycogen storage disease in adult brothers--with special reference to association of gout]. Hirao N; Nobunaga M; Shimazu Y; Kawamura T; Fukuda M Ryumachi; 1972 Nov; 12(3):214-25. PubMed ID: 4514491 [No Abstract] [Full Text] [Related]
14. Prenatal diagnosis of glycogen storage disease type 1a by direct mutation detection. Wong LJ Prenat Diagn; 1996 Feb; 16(2):105-8. PubMed ID: 8650119 [TBL] [Abstract][Full Text] [Related]
15. No mutation in the SLC2A2 ( GLUT2) gene in a Turkish infant with Fanconi-Bickel syndrome. Ozer EA; Aksu N; Uclar E; Erdogan H; Bakiler AR; Tsuda M; Kitasawa E; Coker M; Ozer E Pediatr Nephrol; 2003 Apr; 18(4):397-8. PubMed ID: 12700970 [TBL] [Abstract][Full Text] [Related]
16. Glycogen storage disease (Type IV): a familial cirrhosis diagnosed by electron microscopy (case report). Kalra V; Arya LS; Nayak NC Indian Pediatr; 1980 Jul; 17(7):625-7. PubMed ID: 6938485 [No Abstract] [Full Text] [Related]
17. Hepatic storage of glycogen in Niemann-Pick disease type B. Smith WE; Kahler SG; Frush DP; Milov DE; Gottfried MR; Chen YT J Pediatr; 2001 Jun; 138(6):946-8. PubMed ID: 11391349 [TBL] [Abstract][Full Text] [Related]
18. Glycogen storage disease type IV, amylopectinosis. Levin B Proc R Soc Med; 1968 Dec; 61(12):1264. PubMed ID: 5248385 [No Abstract] [Full Text] [Related]
19. Identification of a novel mutation (867delA) in the glucose-6-phosphatase gene in two siblings with glycogen storage disease type Ia with different phenotypes. Rake JP; ten Berge AM; Visser G; Verlind E; Niezen-Koning KE; Buys CH; Smit GP; Scheffer H Hum Mutat; 2000 Apr; 15(4):381. PubMed ID: 10737986 [TBL] [Abstract][Full Text] [Related]