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Diagnosis of type 1a and type 1c glycogen storage diseases in adultsBURCHELL, A; JUNG, R. T; LANG, C. C et al.Lancet (British edition). 1987, Num 8541, pp 1059-1062, issn 0140-6736Article

Glycogen storage disease types I and II: Treatment updates : Science Oriented Congress and PatnershipKOEBERL, D. D; KISHNANI, P. S; CHEN, Y. T et al.Journal of inherited metabolic disease. 2007, Vol 30, Num 2, pp 159-164, issn 0141-8955, 6 p.Conference Paper

Glycogen storage disease type I: laboratory data and diagnosisWAKID, N. W; BITAR, J. G; ALLAM, C. K et al.Clinical chemistry (Baltimore, Md.). 1987, Vol 33, Num 11, pp 2008-2010, issn 0009-9147Article

Urinary excretion of lactate, 2-oxoglutarate, citrate, and glycerol in patients with glycogenosis type IFERNANDES, J; BERGER, R.Pediatric research. 1987, Vol 21, Num 3, pp 279-282, issn 0031-3998Article

Emerging therapies for glycogen storage disease type IKOEBERL, D. D; KISHNANI, P. S; BALI, D et al.Trends in endocrinology and metabolism. 2009, Vol 20, Num 5, pp 252-258, issn 1043-2760, 7 p.Article

Neutrophil dysfunction in glycogen storage disease Ib : assocation with Crohn's like colitisCOUPER, R; KAPPELUSHNIK, J; GRIFFITHS, A. M et al.Gastroenterology (New York, NY. 1943). 1991, Vol 100, Num 2, pp 549-554, issn 0016-5085Article

Adenomas in glycogen storage disease type 1: two cases with unusual histologic featuresPOE, R; SNOVER, D. C.The American journal of surgical pathology. 1988, Vol 12, Num 6, pp 477-483, issn 0147-5185Article

Gene therapy for type I glycogen storage diseasesCHOU, Janice Y; MANSFIELD, Brian C.Current gene therapy. 2007, Vol 7, Num 2, pp 79-88, issn 1566-5232, 10 p.Article

Natural History of Hepatocellular Adenoma Formation in Glycogen Storage Disease Type IWANG, David Q; FISKE, Laurie M; CARRERAS, Caroline T et al.The Journal of pediatrics. 2011, Vol 159, Num 3, pp 442-446, issn 0022-3476, 5 p.Article

Vascular Dysfunction in Glycogen Storage Disease Type IBERNIER, Angelina V; CORREIA, Catherine E; HALLER, Michael J et al.The Journal of pediatrics. 2009, Vol 154, Num 4, pp 588-591, issn 0022-3476, 4 p.Article

Psychosocial Functioning in Youth with Glycogen Storage Disease Type ISTORCH, Eric; KEELEY, Mary; MERLO, Lisa et al.Journal of pediatric psychology. 2008, Vol 33, Num 7, pp 728-738, issn 0146-8693, 11 p.Article

Pulmonary arterial hypertension and type-I glycogen-storage disease: the serotonin hypothesisHUMBERT, M; LABRUNE, P; LAUNAY, J-M et al.The European respiratory journal. 2002, Vol 20, Num 1, pp 59-65, issn 0903-1936Article

Effect of liver transplantation on hepatic glucose metabolism in a patient with type I glycogen storage diseasKOESTINGER, A; GILLET, M; CHIOLERO, R et al.Transplantation. 2000, Vol 69, Num 10, pp 2205-2207, issn 0041-1337Article

Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim ArabPARVARI, R; MOSES, S; HERSHKOVITZ, E et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 1, pp 21-27, issn 0141-8955Article

Beneficial effects of fish-oil supplements on lipids, lipoproteins, and lipoprotein lipase in patients with glycogen storage disease type ILEVY, E; THIBAULT, L; TURGEON, J et al.The American journal of clinical nutrition. 1993, Vol 57, Num 6, pp 922-929, issn 0002-9165Article

Tolerance to prolonged fasting in two children with type I glycogen storage diseaseLABRUNE, P; CHALAS, J; BAUSSAN, C et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 6, pp 1044-1045, issn 0141-8955Article

Isolation of the gene for murine glucose-6-phosphatase, the enzyme difficient in glycogen storage disease type 1ASHELLY, L. L; KEI-JIAN LEI; CHI-JIUNN PAN et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 29, pp 21482-21485, issn 0021-9258Article

Glycogen storage disease Ib: modification of α₁-antitrypsin glycoprotein microheterogeneityHEYNE, K; HENKE-WOLTER, J.European journal of pediatrics. 1989, Vol 148, Num 4, pp 341-343, issn 0340-6199, 3 p.Article

Study of liver metabolism in glucose-6-phosphatase deficiency (glycogen storage disease type 1A) by P-31 magnetic resonance spectroscopyOBERHAENSLI, R. D; RAJAGOPALAN, B; TAYLOR, D. J et al.Pediatric research. 1988, Vol 23, Num 4, pp 375-380, issn 0031-3998Article

Absence of the SRC-2 Coactivator Results in a Glycogenopathy Resembling Von Gierke's DiseaseCHOPRA, Atul R; LOUET, Jean-Francois; CHAN, Lawrence et al.Science (Washington, D.C.). 2008, Vol 322, Num 5906, pp 1395-1399, issn 0036-8075, 5 p.Article

Clinical evaluation of a portable lactate meter in type I glycogen storage diseaseSAUNDERS, A. C; FELDMAN, H. A; CORREIA, C. E et al.Journal of inherited metabolic disease. 2005, Vol 28, Num 5, pp 695-701, issn 0141-8955, 7 p.Article

Glucose production in glycogen storage disease I is not associated with increased cycling through hepatic glycogenROTHER, K. I; SCHWENK, W. F.American journal of physiology. Endocrinology and metabolism. 1995, Vol 32, Num 4, pp E774-E778, issn 0193-1849Article

Orthotopic liver transplantation for type I glycogenosis unresponsive to medical therapySOKAL, E. M; LOPEZ-SILVARREY, A; BUTS, J. P et al.Journal of pediatric gastroenterology and nutrition. 1993, Vol 16, Num 4, pp 465-467, issn 0277-2116Article

Effect of granulocyte-colony stimulating factor in glycogen storage disease type IBZUCCOTTI, G. V; LONGHI, R; FLUMINE, P et al.Journal of international medical research. 1993, Vol 21, Num 5, pp 276-279, issn 0300-0605Article