glutamic acid and Amino Acid Metabolism Disorders, Inborn
glutamic acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 24 studies
Research
Studies (24)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (16.67) | 18.7374 |
1990's | 6 (25.00) | 18.2507 |
2000's | 6 (25.00) | 29.6817 |
2010's | 7 (29.17) | 24.3611 |
2020's | 1 (4.17) | 2.80 |
Authors
Authors | Studies |
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Antunes Soares, FA; Aschner, M; Bicca Obetine Baptista, F; Duarte Hartmann, D; Farina Gonçalves, D; Franzen da Silva, A; Lenz Dalla Corte, C; Limana da Silveira, T; Lopes Machado, M; Marafiga Cordeiro, L | 1 |
Barbieri Caus, L; Calcagnotto, ME; Ganzella, M; Gomes de Souza, DO; Goodman, S; Junges, B; Koeller, DM; Loureiro, S; Meier, L; Umpierrez Amaral, A; Vendramin Pasquetti, M; Wajner, M; Woontner, M | 1 |
He, Z; Wang, L; Xia, H; Ye, J; Zhu, J | 1 |
Kölker, S | 1 |
Bogo, MR; Bonan, CD; de Oliveira, DL; Mussulini, BHM; Rico, EP; Rosemberg, DB; Savio, LEB; Vuaden, FC; Wyse, ATS | 1 |
Amaral, AU; Castilho, RF; Cecatto, C; Wajner, M | 1 |
Anderson, G; Benatti, M; Brown, R; Chong, K; Clayton, PT; Footitt, E; Gissen, P; Hemingway, C; Holden, S; James, C; Little, D; Mills, PB; Ocaka, L; Parker, A; Rahman, S; Reid, ES; Williams, H | 1 |
Braga, A; da Cunha, AA; da Cunha, MJ; Ferreira, AG; Machado, FR; Moreira, JD; Mussulini, BH; Scherer, EB; Souza, DO; Wofchuk, S; Wyse, AT | 1 |
AKABANE, J; MINAGAWA, A; MIZUNO, T; MORIKAWA, T; OGASAWARA, J; OKAMURA, T; TADA, K; WADA, Y; YOSHIDA, T | 1 |
Erb, M; Ethofer, T; Grodd, W; Kardatzki, B; Klose, U; Kraft, E; Landwehrmeyer, GB; Seeger, U; Storch, A | 1 |
de Mello, CF; Hoffmann, GF; Kölker, S; Souza, DO; Wajner, M | 1 |
Levy, HL | 1 |
Ashurst, CL; Ernst, SL; Filipowicz, HR; Longo, N; Pasquali, M | 1 |
Cheng, KC; Connor, JR; Goodman, SI; Housman, C; Jacobs, RE; LaNoue, K; Lazovic, J; O'Callaghan, JP; Simpson, I; Woontner, M; Zinnanti, WJ | 1 |
Gray, RG; Hill, SE; Pollitt, RJ | 1 |
Baltassat, P; Cotte, J; Divry, P; Duran, M; Hermier, M; Rolland, MO; Wadman, SK | 1 |
Nicklas, WJ | 1 |
Butterworth, RF; Qureshi, IA; Ratnakumari, L | 1 |
Franz, AR; Pohlandt, F | 1 |
Korinthenberg, R | 1 |
Akatsu, T; Kawamoto, S; Kerlin, P; Kobayashi, K; Lynch, SV; Matsunami, H; Nakagawa, S; Saheki, T; Steadman, C; Strong, RW | 1 |
Coitinho, AS; Dal-Pizzol, A; Emanuelli, T; Porciúncula, LO; Souza, DO; Wajner, M | 1 |
Kameyama, M; Sawada, H; Seriu, N; Sugiyama, H; Udaka, F | 1 |
Chang, LJ; Deck, J; el-Awar, M; Gilbert, J; Kish, SJ; Robitaille, Y; Schut, L | 1 |
Reviews
3 review(s) available for glutamic acid and Amino Acid Metabolism Disorders, Inborn
Article | Year |
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Metabolism of amino acid neurotransmitters: the synaptic disorder underlying inherited metabolic diseases.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Developmental Disabilities; gamma-Aminobutyric Acid; Glutamic Acid; Humans; Multifactorial Inheritance; Neurotransmitter Agents; Succinate-Semialdehyde Dehydrogenase | 2018 |
Modulation of glutamatergic and GABAergic neurotransmission in glutaryl-CoA dehydrogenase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; gamma-Aminobutyric Acid; Glutamic Acid; Glutaryl-CoA Dehydrogenase; Humans; Neurotoxins; Oxidoreductases Acting on CH-CH Group Donors; Synaptic Transmission | 2004 |
Amino acid metabolism in the central nervous system: role of glutamate dehydrogenase.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Central Nervous System; Cerebellar Ataxia; Enzyme Activation; gamma-Aminobutyric Acid; Glutamate Dehydrogenase; Glutamate Synthase; Glutamates; Glutamic Acid; Glutamine; Humans; Leucine; Mitochondria; NADP; Nerve Endings; Neuroglia; Rats; Syndrome | 1984 |
Other Studies
21 other study(ies) available for glutamic acid and Amino Acid Metabolism Disorders, Inborn
Article | Year |
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Caenorhabditis elegans as a model for studies on quinolinic acid-induced NMDAR-dependent glutamatergic disorders.
Topics: 1-Octanol; Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Animals; Animals, Genetically Modified; Caenorhabditis elegans; Citrate (si)-Synthase; Disease Models, Animal; Glutamic Acid; Humans; Kynurenine; Motor Activity; Neurodegenerative Diseases; Quinolinic Acid; Receptors, N-Methyl-D-Aspartate; Signal Transduction; Synaptic Transmission | 2021 |
Impairment of GABAergic system contributes to epileptogenesis in glutaric acidemia type I.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Blotting, Western; Brain; Brain Diseases, Metabolic; Chromatography, High Pressure Liquid; Epilepsy; GABA Antagonists; gamma-Aminobutyric Acid; Glutamate Decarboxylase; Glutamic Acid; Glutaryl-CoA Dehydrogenase; Mice; Mice, Knockout; Pentylenetetrazole; Synaptosomes | 2017 |
A case of severe glutathione synthetase deficiency with novel GSS mutations.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Glutamic Acid; Glutathione Synthase; Humans; Infant, Newborn; Male; Mutation; Pyroglutamate Hydrolase; Sequence Analysis, DNA | 2018 |
Methionine Exposure Alters Glutamate Uptake and Adenine Nucleotide Hydrolysis in the Zebrafish Brain.
Topics: Adenosine; Adenosine Triphosphatases; Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Animals; Brain; Glutamic Acid; Glycine N-Methyltransferase; Hydrolysis; Methionine; Zebrafish | 2016 |
2-Methylcitric acid impairs glutamate metabolism and induces permeability transition in brain mitochondria.
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Animals; Brain; Calcium; Citrates; Cyclosporine; Energy Metabolism; Glutamate Dehydrogenase; Glutamic Acid; Humans; Ketoglutaric Acids; Malates; Male; Membrane Potential, Mitochondrial; Mitochondria; Mitochondrial Membrane Transport Proteins; Mitochondrial Permeability Transition Pore; Oxidative Phosphorylation; Oxygen Consumption; Propionic Acidemia; Pyruvic Acid; Rats; Rats, Wistar | 2016 |
Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Developmental Disabilities; Female; Fibroblasts; Glutamic Acid; Humans; Infant; Infant, Newborn; Male; Mitochondria; Mitochondria, Liver; Mitochondrial Membrane Transport Proteins; Muscle Hypotonia; Mutation; Proline; Seizures | 2017 |
Evidence that hyperprolinemia alters glutamatergic homeostasis in rat brain: neuroprotector effect of guanosine.
Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Animals; Blotting, Western; Brain; Glutamic Acid; Guanosine; Homeostasis; Neuroprotective Agents; Proline Oxidase; Rats; Rats, Wistar; Sodium-Potassium-Exchanging ATPase; Thiobarbituric Acid Reactive Substances | 2012 |
A SEX-LINKED DISORDER WITH MENTAL AND PHYSICAL RETARDATION CHARACTERIZED BY CEREBROCORTICAL ATROPHY AND INCREASE OF GLUTAMIC ACID IN THE CEREBROSPINAL FLUID.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Atrophy; Blood; Brain Diseases; Cerebrospinal Fluid; Chromosomes; Galactose; Genetics, Medical; Glutamates; Glutamic Acid; Glutamine; Growth; Humans; Intellectual Disability; Kidney; Renal Aminoacidurias; Urine | 1964 |
Proton MR spectroscopy in succinic semialdehyde dehydrogenase deficiency.
Topics: Adult; Aldehyde Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Brain; gamma-Aminobutyric Acid; Genes, Recessive; Glutamic Acid; Glutamine; Humans; Hydroxybutyrates; Magnetic Resonance Spectroscopy; Male; Movement Disorders; Predictive Value of Tests; Protons; Reference Values; Seizures; Speech Disorders; Succinate-Semialdehyde Dehydrogenase | 2004 |
Metabolic disorders in the center of genetic medicine.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic, Inborn; Glutamate-Ammonia Ligase; Glutamic Acid; Glutamine; Homocystinuria; Humans; Hyperhomocysteinemia; Infant, Newborn; Mutation; Phenylketonurias | 2005 |
Metabolic changes associated with hyperammonemia in patients with propionic acidemia.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Glutamic Acid; Glutamine; Humans; Hyperammonemia; Infant; Infant, Newborn; Propionates | 2006 |
Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type I.
Topics: Aging; Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Child; Diet; Disease Models, Animal; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glucose; Glutamic Acid; Glutarates; Glutaryl-CoA Dehydrogenase; Homoarginine; Humans; Lysine; Mice; Mice, Knockout; Mitochondria; Neurons; Nuclear Magnetic Resonance, Biomolecular; Tryptophan | 2007 |
Reduced ornithine catabolism in cultured fibroblasts and phytohaemagglutinin-stimulated lymphocytes from a patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Aspartate Ammonia-Lyase; Cells, Cultured; Citrulline; Fibroblasts; Glutamates; Glutamic Acid; Humans; Lymphocyte Activation; Lymphocytes; Ornithine; Phytohemagglutinins; Proline | 1982 |
A new patient with 4-hydroxybutyric aciduria, a possible defect of 4-aminobutyrate metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; gamma-Aminobutyric Acid; Glutamates; Glutamic Acid; Humans; Hydroxybutyrate Dehydrogenase; Hydroxybutyrates; Male; Sodium Oxybate; Valproic Acid | 1983 |
Effect of L-carnitine on cerebral and hepatic energy metabolites in congenitally hyperammonemic sparse-fur mice and its role during benzoate therapy.
Topics: Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Benzoates; Benzoic Acid; Body Weight; Brain; Brain Chemistry; Carnitine; Coenzyme A; Dose-Response Relationship, Drug; Energy Metabolism; Genetic Linkage; Glutamates; Glutamic Acid; Glutamine; Hair Diseases; Ketoglutaric Acids; Lactates; Liver; Male; Mice; Mice, Mutant Strains; Ornithine Carbamoyltransferase; Pyruvates; Time Factors; Urea | 1993 |
Transient glutamic acidaemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Bottle Feeding; Breast Feeding; Diagnosis, Differential; Diarrhea, Infantile; Diseases in Twins; Follow-Up Studies; Glutamic Acid; Humans; Infant; Infant, Newborn; Male; Twins, Dizygotic | 1996 |
Is infantile alternating hemiplegia mediated by glutamate toxicity and can it be treated with memantine?
Topics: Amino Acid Metabolism, Inborn Errors; Child; Excitatory Amino Acid Antagonists; Glutamic Acid; Hemiplegia; Humans; Male; Memantine | 1996 |
Orthotopic liver transplantation for adult-onset type II citrullinaemia.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Ammonia; Arginine; Argininosuccinate Synthase; Brain Edema; Cause of Death; Citrulline; Diet, Protein-Restricted; Disease Progression; Fatal Outcome; Glutamic Acid; Hepatic Encephalopathy; Humans; Immunohistochemistry; Liver; Liver Transplantation; Male; Prognosis; Referral and Consultation | 1997 |
Inhibition of synaptosomal [3H]glutamate uptake and [3H]glutamate binding to plasma membranes from brain of young rats by glutaric acid in vitro.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Transport System X-AG; Animals; ATP-Binding Cassette Transporters; Cell Membrane; Convulsants; Depression, Chemical; gamma-Aminobutyric Acid; Glutamate Decarboxylase; Glutamic Acid; Glutarates; Glutaryl-CoA Dehydrogenase; Male; Nerve Tissue Proteins; Neurotoxins; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Rats; Rats, Wistar; Sodium; Synaptosomes | 2000 |
Cerebellar ataxia with glutamic aciduria.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Arginine; Atrophy; Cerebellum; Cystinuria; Female; Glutamates; Glutamic Acid; Humans; Kidney Tubules; Lysine; Magnetic Resonance Imaging; Ornithine; Spinocerebellar Degenerations | 1991 |
Brain amino acid reductions in one family with chromosome 6p-linked dominantly inherited olivopontocerebellar atrophy.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aspartic Acid; Brain Chemistry; Chromosomes, Human, Pair 6; Ethanolamines; gamma-Aminobutyric Acid; Genes, Dominant; Glutamates; Glutamic Acid; Glutamine; Humans; Middle Aged; Olivopontocerebellar Atrophies; Taurine | 1991 |