Les glycogénoses de type 1b et 1c = Glycogen storage diseases type 1b and 1cDE PARSCAU, L; GUIBAUD, P; MAIRE, I et al.Pédiatrie (Marseille). 1988, Vol 43, Num 8, pp 661-665, issn 0031-4021Article

Glycogénose de type I: une nouvelle observation = Type I glycogenosis. Report of a new caseLE LUYER, B; MOUTERNE, O; CHABROLLE, J. P et al.Revue de pédiatrie (Paris). 1986, Vol 22, Num 2, pp 61-69, issn 0035-1644Article

Glycogen storage disease type IbSCHAUB, J; HEYNE, K.European journal of pediatrics. 1983, Vol 140, Num 4, pp 283-288, issn 0340-6199Article

Cornstarch therapy in type I glycogen-storage diseaseYUAN-TSONG CHEN; CORNBLATH, M; SIDBURY, J. B et al.The New England journal of medicine. 1984, Vol 310, Num 3, pp 171-175, issn 0028-4793Article

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

The serum apolipoprotein profile of patients with glucose-6-phosphatase deficiencyALAUPOVIC, P; FERNANDES, J.Pediatric research. 1985, Vol 19, Num 4, pp 380-384, issn 0031-3998Article

Glucose production and utilization in children with glycogen storage disease type ITSALIKIAN, E; SIMMONS, P; GERICH, J. E et al.American journal of physiology. Endocrinology and metabolism. 1984, Vol 10, Num 4, pp E513-E519, issn 0193-1849Article

Impaired metabolic function of polymorphonuclear leukocytes in glycogen storage disease IbGAHR, M; HEYNE, K.European journal of pediatrics. 1983, Vol 140, Num 4, pp 329-330, issn 0340-6199Article

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

Glycogen storage disease: effects of glucose infusions on [¹⁵N] glycine kinetics and nitrogen metabolismYUDKOFF, M; NISSIM, I; STANLEY, C et al.Journal of pediatric gastroenterology and nutrition. 1984, Vol 3, Num 1, pp 81-88, issn 0277-2116Article

Biochemical diagnosis of type 1b glycogen storage diseaseHAWKINS, R. A; KAMATH, K. R; DORNEY, J. F. A et al.Australian paediatric journal. 1984, Vol 20, Num 3, pp 217-220, issn 0004-993XArticle

Diet and growth of children with glycogen storage disease type I and IIIDAESCHEL, I. E; JANICK, L. S; KRAMISH, M. J et al.Journal of the American Dietetic Association. 1983, Vol 83, Num 2, pp 135-141, issn 0002-8223Article

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

The role of raw starches in the treatment of type I glycogenosisSIDBURY, J. B; YUAN-TSONG CHEN; ROE, C. R et al.Archives of internal medicine (1960). 1986, Vol 146, Num 2, pp 370-373, issn 0003-9926Article

Neutropenia and impaired neutrophil function in glycogenosis type IbDI ROCCO, M; BORRONE, C; DALLEGRI, F et al.Journal of inherited metabolic disease. 1984, Vol 7, Num 4, pp 151-154, issn 0141-8955Article

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