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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
Journal Article
BBA - Bioenergetics, ISSN 0005-2728, 08/2016, Volume 1857, pp. e98 - e98
Journal Article
Molecular Therapy, ISSN 1525-0016, 03/2018, Volume 26, Issue 3, pp. 890 - 901
Glycogen storage disease type III (GSDIII) is an autosomal recessive disorder caused by a deficiency of glycogen-debranching enzyme (GDE), which results in... 
dual AAV vectors | acid-alpha-glucosidase | neuromuscular disease | gene therapy | glycogen storage disease type III | glycogenosis | Cori disease | adeno-associated vector | MEDICINE, RESEARCH & EXPERIMENTAL | EFFICACY | ADENOASSOCIATED VIRUS | TRANSDUCTION | GENOME | THERAPY | GLYCOGEN-STORAGE-DISEASE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | AAV | MOUSE MODEL | IN-VIVO | GENETICS & HEREDITY | VECTORS | Dependovirus - genetics | Glycogen Storage Disease Type III - metabolism | Genetic Vectors - administration & dosage | Male | Muscle, Skeletal - metabolism | Hepatocytes - metabolism | Glycogen - metabolism | Glycogen Debranching Enzyme System - genetics | Disease Models, Animal | Gene Transfer Techniques | Gene Expression | Glycogen Storage Disease Type III - therapy | Glycogen Debranching Enzyme System - metabolism | Glycogen Storage Disease Type III - diagnosis | Liver - metabolism | Blood Glucose | Organ Specificity | Genetic Vectors - genetics | Glycogen Storage Disease Type III - genetics | Mice, Knockout | Phenotype | Animals | Biomarkers | Mice | Enzyme Activation | Genetic Therapy - methods | Genetic Therapy | Biotechnology | Liver | Life Sciences | Genetics | Glycogen Debranching Enzyme System | Glycogen | Biochemistry, Molecular Biology | Glycogen Storage Disease Type III | Dependovirus | Hepatocytes | Muscle, Skeletal | Genetic Vectors | Molecular biology | Human genetics | Original
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BBA - General Subjects, ISSN 0304-4165, 01/2017, Volume 1861, Issue 1, pp. 3388 - 3398
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The EMBO Journal, ISSN 0261-4189, 08/2004, Volume 23, Issue 16, pp. 3196 - 3205
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Nature communications, ISSN 2041-1723, 2018, Volume 9, Issue 1, pp. 1126 - 15
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