Glycogen metabolism inborn errors. Medical search. Frequent questions

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Anatomy7

Liver Muscle, Skeletal Muscles Cells, Cultured Brain Fibroblasts Microsomes, Liver

Organisms6

Rats, Inbred Strains Rats, Wistar Rabbits Saccharomyces cerevisiae Mice, Knockout Rats, Sprague-Dawley

Diseases51

Metabolism, Inborn Errors Amino Acid Metabolism, Inborn Errors Glycogen Storage Disease Lafora Disease Lipid Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Steroid Metabolism, Inborn Errors Carbohydrate Metabolism, Inborn Errors Urea Cycle Disorders, Inborn Brain Diseases, Metabolic, Inborn Argininosuccinic Aciduria Hyperammonemia Phenylketonurias Smith-Lemli-Opitz Syndrome Refractive Errors Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors Glycogen Storage Disease Type I Fabry Disease Ornithine Carbamoyltransferase Deficiency Disease Hypophosphatasia Brain Diseases, Metabolic Metal Metabolism, Inborn Errors Fructose Metabolism, Inborn Errors Maple Syrup Urine Disease Metabolic Diseases Porphyria, Erythropoietic Glycogen Storage Disease Type II Hyperargininemia Failure to Thrive Iron Metabolism Disorders Alkaptonuria Rare Diseases Citrullinemia Multiple Acyl Coenzyme A Dehydrogenase Deficiency Mucopolysaccharidoses Glycogen Storage Disease Type III Pyruvate Dehydrogenase Complex Deficiency Disease Lysosomal Storage Diseases Neuroaxonal Dystrophies Hyperoxaluria, Primary Genetic Diseases, Inborn Renal Tubular Transport, Inborn Errors Glycogen Storage Disease Type IV Glycogen Storage Disease Type V Starvation Liver Diseases Disease Models, Animal Intellectual Disability Nervous System Diseases

Chemicals and Drugs86

Glycogen Glycogen Synthase Glycogen Phosphorylase Liver Glycogen Phosphorylases Phosphorylase a Glycogen Synthase Kinase 3 Glucose Glycogen Debranching Enzyme System 1,4-alpha-Glucan Branching Enzyme Glucose-6-Phosphate Protein Phosphatase 1 Glucosephosphates Phosphorylase Kinase Phosphoprotein Phosphatases Insulin Uridine Diphosphate Glucose Glycogen Synthase Kinases Lactates Glycogen-Synthase-D Phosphatase Dextrins Glucagon Phosphoglucomutase Lactic Acid Glucosyltransferases Protein Tyrosine Phosphatases, Non-Receptor Blood Glucose Glucokinase alpha-Glucosidases Phosphorylase Phosphatase Dual-Specificity Phosphatases Carbon Isotopes Adenosine Monophosphate Epinephrine Homogentisate 1,2-Dioxygenase alpha-Galactosidase Cyclic AMP Argininosuccinic Acid Isovaleryl-CoA Dehydrogenase Methylmalonic Acid Carnitine Adenosine Triphosphate Hydroxocobalamin Pentanoic Acids Methylmalonyl-CoA Mutase Oxidoreductases Acting on CH-CH Group Donors Muscle Proteins Glutarates Amidinotransferases Carrier Proteins Protein Kinases Glutaryl-CoA Dehydrogenase Protein-Serine-Threonine Kinases Phosphorylase b Glycogen Phosphorylase, Liver Form Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Glycogen Phosphorylase, Muscle Form Fatty Acids Adenylosuccinate Lyase Acyl-CoA Dehydrogenase Ornithine-Oxo-Acid Transaminase Ammonia Lithium Chloride Argininosuccinate Lyase Oxidoreductases Urea Carbon Radioisotopes Uroporphyrinogen III Synthetase Ornithine Cholesterol Cytochrome P-450 Enzyme System Glucose-6-Phosphatase Amino Acids Fatty Acids, Nonesterified Phenylalanine Hydroxylase Glycogen Phosphorylase, Brain Form Hexokinase Acyl-CoA Dehydrogenases Bile Acids and Salts Deoxyglucose Carbon Vitamin B 12 Dietary Carbohydrates Enzyme Inhibitors Triglycerides Pyruvic Acid

Analytical, Diagnostic and Therapeutic Techniques and Equipment17

Neonatal Screening Magnetic Resonance Spectroscopy Models, Biological Perfusion Diagnostic Errors Mass Spectrometry Reference Values Pedigree Gas Chromatography-Mass Spectrometry Tandem Mass Spectrometry Phlebotomy Reproducibility of Results Blood Specimen Collection Diet, Protein-Restricted Chromatography, High Pressure Liquid DNA Mutational Analysis Disease Models, Animal

Psychiatry and Psychology2

Fasting Intellectual Disability

Phenomena and Processes30

Glycogenolysis Energy Metabolism Gluconeogenesis Glycolysis Lipid Metabolism Mutation Kinetics Enzyme Activation Phosphorylation Carbohydrate Metabolism Time Factors Fasting Amino Acid Sequence Metabolism Signal Transduction Metabolic Networks and Pathways Phenotype Base Sequence Oxidation-Reduction Homozygote Oxygen Consumption Biotransformation Diet, Protein-Restricted Consanguinity Mutation, Missense Genotype Heterozygote Citric Acid Cycle Algorithms Biological Transport

Technology, Industry, Agriculture1

Dietary Carbohydrates

Information Science4

Molecular Sequence Data Amino Acid Sequence Base Sequence Algorithms

Named Groups1

Infant, Newborn

Health Care5

Neonatal Screening Diagnostic Errors Critical Pathways Reproducibility of Results Technology Assessment, Biomedical

Geographicals1

Australian Capital Territory

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Technology, Industry, Agriculture Information Science Named Groups Health Care Geographicals

Glycogen Metabolism, Inborn Errors Glycogen Synthase Glycogen Phosphorylase Liver Glycogen Phosphorylases Amino Acid Metabolism, Inborn Errors Phosphorylase a Glycogen Synthase Kinase 3 Glucose Glycogen Debranching Enzyme System Glycogenolysis Glycogen Storage Disease 1,4-alpha-Glucan Branching Enzyme Liver Glucose-6-Phosphate Protein Phosphatase 1 Glucosephosphates Lafora Disease Phosphorylase Kinase Lipid Metabolism, Inborn Errors Phosphoprotein Phosphatases Insulin Neonatal Screening Purine-Pyrimidine Metabolism, Inborn Errors Energy Metabolism Steroid Metabolism, Inborn Errors Gluconeogenesis Uridine Diphosphate Glucose Glycolysis Muscle, Skeletal Carbohydrate Metabolism, Inborn Errors Glycogen Synthase Kinases Lactates Muscles Glycogen-Synthase-D Phosphatase Dextrins Urea Cycle Disorders, Inborn Glucagon Phosphoglucomutase Brain Diseases, Metabolic, Inborn Lactic Acid Glucosyltransferases Protein Tyrosine Phosphatases, Non-Receptor Argininosuccinic Aciduria Blood Glucose Lipid Metabolism Glucokinase Hyperammonemia alpha-Glucosidases Mutation Kinetics Phosphorylase Phosphatase Dual-Specificity Phosphatases Rats, Inbred Strains Magnetic Resonance Spectroscopy Phenylketonurias Carbon Isotopes Molecular Sequence Data Smith-Lemli-Opitz Syndrome Enzyme Activation Adenosine Monophosphate Epinephrine Phosphorylation Models, Biological Rats, Wistar Carbohydrate Metabolism Time Factors Infant, Newborn Cells, Cultured Refractive Errors Homogentisate 1,2-Dioxygenase Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors Fasting alpha-Galactosidase Amino Acid Sequence Glycogen Storage Disease Type I Fabry Disease Cyclic AMP Rabbits Australian Capital Territory Ornithine Carbamoyltransferase Deficiency Disease Argininosuccinic Acid Isovaleryl-CoA Dehydrogenase Hypophosphatasia Perfusion Metabolism Methylmalonic Acid Carnitine Diagnostic Errors Brain Diseases, Metabolic Adenosine Triphosphate Hydroxocobalamin Pentanoic Acids Methylmalonyl-CoA Mutase Oxidoreductases Acting on CH-CH Group Donors Signal Transduction Metal Metabolism, Inborn Errors

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