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

An investigation of the possible influence of neutral α-glucosidases on the clinical heterogeneity of glycogenosis type IIVAN DER PLOEG, A. T; KROOS, M. A; SWALLOW, D. M et al.Annals of human genetics. 1989, Vol 53, Num 2, pp 185-192, issn 0003-4800, 8 p.Article

Evolution à long terme des glycogénoses hépatiques: étude rétrospective de 76 observations = Long term outcome of hepatic glycogen storage diseases: a retrospective study of 76 patientsDE PARSCAU, L; GUIBAUD, P; LABRUNE, P et al.Archives françaises de pédiatrie. 1988, Vol 45, Num 9, pp 641-645, issn 0003-9764Article

Glycogen storage disease research and clinical problems: a reappraisalHOWELL, R. R.Journal of pediatric gastroenterology and nutrition. 1984, Vol 3, Num 1, pp 12-13, issn 0277-2116Article

LABORATORY DIAGNOSIS OF THE NEUROMUSCULAR GLYCOGEN STORAGE DISEASESFARMER PM.1982; ANNALS OF CLINICAL AND LABORATORY SCIENCE; ISSN 0091-7370; USA; DA. 1982; VOL. 12; NO 6; PP. 431-438; BIBL. 62 REF.Article

Kinetic studies on the glucose-6-phosphate transport system in rat hepatic microsomal membraneIGARASHI, Y; KATO, S; TADA, K et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 277-279, issn 0141-8955, suppl. 2Conference Paper

New aspects of diagnosis and treatment of glycogen storage diseaseROSENFELD, E. L.Biologisches Zentralblatt. 1984, Vol 103, Num 2, pp 139-146, issn 0006-3304Article

Liver-spleen scintigraphy in glycogen storage disease (glycogenoses)HEYMAN, S.Clinical nuclear medicine. 1985, Vol 10, Num 12, pp 839-843, issn 0363-9762Article

Etude cytochimique de la conformation du glycogène hépatique dans deux cas de glycogénose = Cytochemical study of liver glycogen in two cases of glycogenosisBENKOEL, L; GULIAN, J. M; CHAMLIAN, A et al.Cellular and molecular biology. 1984, Vol 30, Num 2, pp 145-152, issn 0145-5680Article

Abnormal oligosaccharide pattern in glycogen storage disease type IIIGALVIN-PARTON, P; HOMMES, F. A.Journal of inherited metabolic disease. 1996, Vol 19, Num 3, pp 383-384, issn 0141-8955Article

Glucose recycling and production in glycogenosis type I and III: stable isotope technique studyHALDERON, B; KORMAN, S. H; GUTMAN, A et al.American journal of physiology. Endocrinology and metabolism. 1989, Vol 20, Num 3, pp E346-E353, issn 0193-1849Article

Long-term cornstarch therapy in glycogen storage disease types I, Ib and IIIGATTI, R; LAMEDICA, G; DI ROCCO, M et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 280-283, issn 0141-8955, suppl. 2Conference Paper

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

Diagnosis of type 1B and 1C glycogen storage diseaseBURCHELL, A; GIBB, L.Journal of inherited metabolic disease. 1991, Vol 14, Num 3, pp 305-307, issn 0141-8955Article

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

Erythrocyte glycolysis and its marked alteration by muscular exercise in type VII glycogenosisSHIMIZU, T; KONO, N; KIYOKAWA, H et al.Blood. 1988, Vol 71, Num 4, pp 1130-1134, issn 0006-4971Article

GLUCOSE-CONTAINING OLIGOSACCHARIDES IN THE URINE OF PATIENTS WITH GLYCOGEN STORAGE DISEASE TYPE II AND TYPE III.LENNARTSON G; LUNDBLAD A; LUNDSTEN J et al.1978; EUROP. J. BIOCHEM.; GERM.; DA. 1978; VOL. 83; NO 2; PP. 325-334; BIBL. 18 REF.Article

A PROPOS DE DEUX CAS DE MALADIE DE POMPE (GLYCOGENOSE CARDIAQUE INFANTILE). REVUE ET DISCUSSION DES PRINCIPALES OBSERVATIONS DE LA LITTERATURE.AJUM KHODABUX.1976; MONTPELLIER; UNIVERSEL COPIE; DA. 1976; PP. (90P.); H.T. 3; BIBL. 12 P.; (THESE DOCT. MED.; MONTPELLIER)Thesis

Lysosomal glycogen storage disease without acid maltase deficiency - a lectin-histochemical study of an unusual type of lysosomal glycogen storage diseaseKASHIO, N; USUKI, F; HIGUCHI, I et al.Acta histochemica et cytochemica. 1991, Vol 24, Num 6, pp 603-611, issn 0044-5991Article

McArdle disease : Another systemic low-inflammation disorder?LUCIA, Alejandro; SMITH, Lucille; NAIDOO, Melissa et al.Neuroscience letters. 2008, Vol 431, Num 2, pp 106-111, issn 0304-3940, 6 p.Article

Pregnancy associated with amylo-1,6-glucosidase deficiency (Forbés disease): case reportCONFINO, E; PAUZNER, D; LIDOR, A et al.British journal of obstetrics and gynaecology (Print). 1984, Vol 91, Num 5, pp 494-497, issn 0306-5456Article

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

Glycogenosis Ib: neutrophil microbicidal defects due to impaired hexose monophosphate shuntSEGER, R; STEINMANN, B; TIEFENAUER, L et al.Pediatric research. 1984, Vol 18, Num 3, pp 297-299, issn 0031-3998Article

Zonal differences of α-glucosidases in human kidney: studies in controls and in patients with glycogenosis type IIPFISTER, K; GITZELMANN, R; STEINMANN, B et al.Clinica chimica acta. 1983, Vol 134, Num 3, pp 307-315, issn 0009-8981Article

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