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Journal of Hepatology, ISSN 0168-8278, 2009, Volume 52, Issue 2, pp. 252 - 257
Hepatocellular carcinoma (HCC) is a common form of cancer that arises from hepatocytes and whose risk may be affected by several known environmental factors,... 
Gastroenterology and Hepatology | Cirrhosis | Hepatitis | Porphyrias | Hemochromatosis | Tyrosinemia type I | Glycogen storage disease | Non-alcoholic steatohepatitis | PRIMARY HEPATOCELLULAR-CARCINOMA | PORPHYRIA-CUTANEA-TARDA | FOLLOW-UP | NONALCOHOLIC STEATOHEPATITIS | HEREDITARY HEMOCHROMATOSIS | DIABETES-MELLITUS | GLYCOGEN-STORAGE-DISEASE | PRIMARY LIVER-CANCER | Tyrosinemia type 1 | HEPATITIS-B | GASTROENTEROLOGY & HEPATOLOGY | VIRAL-HEPATITIS | Humans | Hypothyroidism - complications | Fatty Liver - complications | Male | Porphyrias, Hepatic - genetics | Glycogen Storage Disease Type I - complications | Liver Neoplasms - etiology | Hemochromatosis - complications | Carcinoma, Hepatocellular - genetics | Female | Carcinoma, Hepatocellular - etiology | Diabetes Complications - genetics | Hepatitis, Autoimmune - genetics | Hemochromatosis - genetics | Fatty Liver - genetics | alpha 1-Antitrypsin Deficiency - genetics | Genetic Predisposition to Disease | Liver Neoplasms - genetics | Risk Factors | Tyrosinemias - genetics | Diabetes Complications - etiology | Tyrosinemias - complications | Hepatitis, Autoimmune - complications | Glycogen Storage Disease Type I - genetics | alpha 1-Antitrypsin Deficiency - complications | Models, Genetic | Porphyrias, Hepatic - complications | Type 2 diabetes | Liver cancer | Histocompatibility antigens | Glycogen | Glutathione transferase | HLA histocompatibility antigens | Genetic research | Genetics | Hepatitis C
Journal Article
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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