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Current Opinion in Clinical Nutrition and Metabolic Care, ISSN 1363-1950, 07/2015, Volume 18, Issue 4, pp. 415 - 421
PURPOSE OF REVIEWGlycogen storage disorders (GSDs) are inborn errors of metabolism with abnormal storage or utilization of glycogen. The present review focuses... 
Glycogen storage disease | Hypoglycemia | Complications | Liver | Metabolic control | Outcome | DIAGNOSIS | metabolic control | complications | liver | DISEASE TYPE-III | NATURAL-HISTORY | DEFICIENCY | PATHOGENESIS | NUTRITION & DIETETICS | THERAPY | GENE | hypoglycemia | ENDOCRINOLOGY & METABOLISM | glycogen storage disease | outcome | Dietary Proteins - administration & dosage | Glycogen Storage Disease Type III - physiopathology | Humans | Liver - physiopathology | Glycogen Storage Disease Type I - complications | Glycogen Storage Disease Type VI - diet therapy | Cardiomyopathies - physiopathology | Glycogen - metabolism | Diet, High-Fat | Glycogen Storage Disease Type III - complications | Dietary Fats - administration & dosage | Liver Cirrhosis - diet therapy | Diet, Carbohydrate-Restricted | Disease Models, Animal | Dietary Carbohydrates - administration & dosage | Glycogen Storage Disease Type I - physiopathology | Cardiomyopathies - diet therapy | Glycogen Storage Disease Type III - diagnosis | Glycogen Storage Disease Type VI - complications | Liver Cirrhosis - complications | Glycogen Storage Disease Type VI - diagnosis | Glycogen Storage Disease Type I - diet therapy | Glycogen Storage Disease Type I - diagnosis | Glycogen Storage Disease Type VI - physiopathology | Animals | Cardiomyopathies - complications | Liver Cirrhosis - physiopathology | Glycogen Storage Disease Type III - diet therapy
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Autophagy, ISSN 1554-8627, 11/2010, Volume 6, Issue 8, pp. 1078 - 1089
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The New England Journal of Medicine, ISSN 0028-4793, 01/2005, Volume 352, Issue 4, pp. 362 - 372
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Journal of Inherited Metabolic Disease, ISSN 0141-8955, 12/2018, Volume 41, Issue 6, pp. 911 - 912
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Virchows Archiv : an international journal of pathology, ISSN 0945-6317, 07/2019, pp. 1 - 16
An abnormal structural form of glycogen (with less branching points or amylopectin-like polysaccharide) called polyglucosan (PG) may accumulate in various... 
Heart | Brain | Phenotypes | Genetic disorders | Cardiomyopathy | Glycogen | Amylopectin | Organs | Disorders | Muscles | Nervous system | Genomes | Coronary artery disease | Skeletal muscle | Eutrophication | Gene sequencing | Storage diseases | Polysaccharides | Bioaccumulation | Structural forms | Skin | Heart diseases | Myopathy
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Lancet, The, ISSN 0140-6736, 2012, Volume 379, Issue 9813, pp. 335 - 341
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