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Archives of Disease in Childhood, ISSN 0003-9888, 06/2019, Volume 104, Issue Suppl 3, p. A123
BackgroundGlycogen Storage Disease (GSD) Type IIIa is a recessively inherited disorder caused by a deficiency in the debranching enzyme amylo-1,6-glucosidase.... 
Journal Article
Comparative medicine, ISSN 1532-0820, 02/2016, Volume 66, Issue 1, pp. 41 - 51
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 04/2018, Volume 19, Issue 1, pp. 54 - 6
Background: Glycogen Storage Disease Type III (GSD III) is a rare autosomal recessive metabolic disorder caused by AGL gene mutation. There is significant... 
Clinical characteristics | Chinese | AGL gene | Glycogen storage disease IIIa | HETEROGENEITY | GUIDELINES | GENETICS & HEREDITY | MUTATIONS | EXERCISE | MOLECULAR ANALYSIS | Medical research | Gene mutations | Creatine kinase | Glycogen | Genes | Medicine, Experimental | Genetic aspects | Creatine | Research | Analysis
Journal Article
Journal Article
International journal of organ transplantation medicine, ISSN 2008-6482, 2017, Volume 8, Issue 4, pp. 217 - 220
Glycogen storage disease (GSD) type IIIa (Forbes-Cori disease) can be associated with severe liver disease. A patient with GSD type IIIa may therefore be a... 
Heart | Puberty | Enzymes | Transplants & implants | Cardiomyopathy | Hypoglycemia | Metabolism | Patients | Esophagus | Abdomen | Biopsy | Hepatology | Mutation | Liver cirrhosis | Age | Glycogen storage disease types III | Cirrhosis | Liver diseases | Case Report | Liver transplantation | Cirrhosis, Glycogen storage disease types III
Journal Article
Romanian Journal of Diabetes, Nutrition and Metabolic Diseases, ISSN 1583-8609, 12/2017, Volume 24, Issue 4, pp. 309 - 313
Background: Glycogen storage disease (GSD) type IIIa is a rare inborn error of metabolism characterized by a deficiency in glycogen disbranching enzymes.... 
Inborn error of metabolism | Medicalnutritional intervention | Glycogen storage disease IIIa | medical-nutritional intervention | inborn error of metabolism
Journal Article
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, ISSN 1003-9406, 08/2017, Volume 34, Issue 4, p. 499
To detect potential mutation of the AGL gene in two siblings affected with glycogen storage disease type IIIa. Clinical data of the two siblings was collected... 
Amino Acid Sequence | Glycogen Debranching Enzyme System - genetics | Humans | Adolescent | Female | Infant | Male | Mutation - genetics | Glycogen Storage Disease Type III - genetics | Siblings
Journal Article
Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva, ISSN 1130-0108, 02/2019, Volume 111, Issue 2, pp. 168 - 169
Type III glycogen storage disease (GSD-III) is an autosomal recessive disorder due to the deficiency of the glycogen debrancher enzyme. 80% of the patients... 
Hepatocellular carcinoma | Type III glycogen storage disease | GASTROENTEROLOGY & HEPATOLOGY | Liver cirrhosis | Liver transplantation
Journal Article
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, ISSN 1003-9406, 08/2015, Volume 32, Issue 4, p. 502
Journal Article
Case reports in genetics, ISSN 2090-6544, 2016, Volume 2016, pp. 8154910 - 5
Background. Glycogen storage disease type III (GSDIII) is a rare metabolic disorder with autosomal recessive inheritance, caused by deficiency of the glycogen... 
Enzymes | Glycogen | Creatine kinase | Analysis | Genes | Genetic research | Genetic aspects | Creatine | Case Report
Journal Article
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, ISSN 0334-018X, 06/2008, Volume 21, Issue 6, pp. 587 - 590
Glycogen storage disease type III (GSD-III) is an autosomal recessive disorder caused by the lack of amylo-1,6-glucosidase (AGL), one of the catalytic domains... 
GENE | Jehovah's Witness | ENDOCRINOLOGY & METABOLISM | glycogen storage disease | PEDIATRICS | amylo-1,6-glucosidase | glycogen storage disease type III | non-ketotic hypoglycemia | glycogen storage disease type IIIa
Journal Article
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