threonine and Amino Acid Metabolism Disorders, Inborn

threonine has been researched along with Amino Acid Metabolism Disorders, Inborn in 27 studies

Research

Studies (27)

Timeframe	Studies, this research(%)	All Research%
pre-1990	24 (88.89)	18.7374
1990's	2 (7.41)	18.2507
2000's	1 (3.70)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
ARATA, D	1
SCHWARTZ, C; SCOTT, EB	1
FARBER, E; SIDRANSKY, H	1
CHILDS, B; NYHAN, WL	1
DAVIDSON, DT; STAMBAUGH, R	1
SHOCKMAN, GD	1
Christensen, E; Christensen, M; Duno, M; Lund, AM; Skovby, F	1
Efron, ML; Mechanic, GL; Shih, VE	1
Krieger, I; Nigro, M	1
Evered, DF	1
Minnie, LJ; Terblanche, SE; van der Westhuizen, BM	1
Reddi, OS	1
de Cespedes, C; Estrada, Y; Loria, AR; Nyhan, WL; Sweetman, L	1
Batshaw, M; Brusilow, S; Kulovich, S; Nyhan, W; Spector, E; Thoene, J; Walser, M	1
John, SW; Laframboise, R; Rozen, R; Scriver, CR	1
Bartlett, K; Halliday, D; Leonard, JV; Thompson, GN; Walter, JH	1
Bundgaard, L; Winther, A	1
Baños, G; Daniel, PM; Moorhouse, SR; Pratt, OE	1
Bergner, H; Münchmeyer, R; Simon, O	1
Burt, D; Emery, AE	1
Barkin, E; Levy, HL	1
Barois, A; Caldera, R; Escourolle, R; Goulon, M; Grosbuis, S; Nouailhat, F	1
Hurwitz, LJ; McCormick, D	1
Hsia, YE; Lilljeqvist, AC; Rosenberg, LE	1
Gusev, EI	1
Berge, T; Borgfors, N; Brun, A; von Studnitz, W	1
Gross, S; Maskaleris, ML; Milhorat, AT	1

Reviews

1 review(s) available for threonine and Amino Acid Metabolism Disorders, Inborn

Article	Year
Advances in amino acid metabolism in mammals. Biochemical Society transactions, 1981, Volume: 9, Issue:1 Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Amino Acids; Animals; Biological Transport; Dietary Proteins; Glutamates; Glycine; Humans; Liver; Mitochondria; Organ Specificity; Ornithine; Purine Nucleotides; Serine; Threonine; Transaminases	1981

Other Studies

26 other study(ies) available for threonine and Amino Acid Metabolism Disorders, Inborn

Article	Year
Mechanism of adaptation to a threoninedeficient diet I. Biochemical aspects of a threonine deficiency. Technical report.; TR. Arctic Aeromedical Laboratory (U.S.), 1960, Volume: 60, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Diet; Liver; Threonine	1960
Histopathology of amino acid deficiencies. II. Threonine. Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1953, Volume: 84, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Threonine	1953
Chemical pathology of acute amino acid deficiencies. I. Morphologic changes in immature rats fed threonine-, methionine-, or histidine-devoid diets. A.M.A. archives of pathology, 1958, Volume: 66, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Diet; Histidine; Methionine; Rats; Threonine	1958
FURTHER OBSERVATIONS OF A PATIENT WITH HYPERGLYCINEMIA. Pediatrics, 1964, Volume: 33 Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Blood; Child; Diet; Diet Therapy; Glycine; Humans; Infections; Isoleucine; Leucine; Leukocyte Count; Methionine; Renal Aminoacidurias; Threonine; Toxicology; Valine	1964
EVALUATION OF THE AMINO ACID EXCRETION PATTERN OF MENTAL RETARDATES AS A SCREENING TECHNIQUE FOR INBORN ERRORS OF METABOLISM. The Journal of pediatrics, 1964, Volume: 65 Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Child; Chromatography; Creatine; Creatinine; Cystine; Glutamates; Glutamine; Glycine; Humans; Infant; Intellectual Disability; Mass Screening; Renal Aminoacidurias; Threonine	1964
Bacterial cell wall synthesis: the effect of threonine depletion. The Journal of biological chemistry, 1959, Volume: 234 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Cell Wall; Threonine	1959
Xanthurenic aciduria due to a mutation in KYNU encoding kynureninase. Journal of inherited metabolic disease, 2007, Volume: 30, Issue:2 Topics: Adenine; Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acid Substitution; Child; DNA Mutational Analysis; Genotype; Guanine; Homozygote; Humans; Hydrolases; Male; Mutation; Pedigree; Threonine; Xanthurenates	2007
Rapid short-column chromatography of amino acids. A method for blood and urine specimens in the diagnosis and treatment of metabolic disease. Analytical biochemistry, 1967, Volume: 20, Issue:2 Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Aminobutyrates; Autoanalysis; Buffers; Chromatography, Ion Exchange; Citrates; Cysteine; Cystine; Glutamates; Glutamine; Glycine; Humans; Hydrogen-Ion Concentration; Hydroxyproline; Isoleucine; Phenylalanine; Proline; Sarcosine; Serine; Threonine; Tyrosine; Valine	1967
Evidence of defective threonine metabolism in non-ketotic hyperglycinaemia. Journal of inherited metabolic disease, 1983, Volume: 6, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Benzoates; Benzoic Acid; Glycine; Humans; Infant; Infant, Newborn; Threonine	1983
Benzoylserine and benzoylthreonine in propionic acidaemia treated with sodium benzoate. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1999, Volume: 89, Issue:12 Topics: Amino Acid Metabolism, Inborn Errors; Female; Humans; Mass Spectrometry; Propionates; Serine; Sodium Benzoate; Threonine	1999
Threoninemia--a new metabolic defect. The Journal of pediatrics, 1978, Volume: 93, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Humans; Infant; Male; Threonine	1978
The diagnosis and management of propionic acidemia. Monographs in human genetics, 1978, Volume: 9 Topics: Amino Acid Metabolism, Inborn Errors; Biotin; Child; Child, Preschool; Female; Follow-Up Studies; Humans; Infant; Isoleucine; Male; Methionine; Propionates; Threonine; Valine	1978
Neonatal citrllinemia: treatment with keto-analogues of essential amino acids. The Journal of pediatrics, 1977, Volume: 90, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Essential; Arginine; Argininosuccinate Synthase; Citrulline; Fibroblasts; Histidine; Humans; Infant; Infant, Newborn; Isoleucine; Leucine; Lysine; Male; Methionine; Phenylalanine; Threonine; Tryptophan; Valine	1977
In vitro and in vivo correlations for I65T and M1V mutations at the phenylalanine hydroxylase locus. Human mutation, 1992, Volume: 1, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Sequence; Animals; Base Sequence; Cell Line; Codon; Exons; Female; France; Genotype; Humans; Isoleucine; Male; Molecular Sequence Data; Mutation; Oligodeoxyribonucleotides; Pedigree; Phenotype; Phenylalanine; Phenylalanine Hydroxylase; Polymerase Chain Reaction; Quebec; Threonine; Transfection	1992
Contribution of aminoacid catabolism to propionate production in methylmalonic acidaemia. Lancet (London, England), 1989, Jun-10, Volume: 1, Issue:8650 Topics: Acyl Coenzyme A; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Humans; Isoleucine; Kinetics; Leucine; Malonates; Methionine; Methylmalonic Acid; Phenylalanine; Threonine; Time Factors; Valine	1989
Argininosuccinic aciduria in hereditary hair diseases. Acta dermato-venereologica, 1968, Volume: 48, Issue:6 Topics: Adolescent; Adult; Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Chromatography, Paper; Cystinuria; Female; Glutamates; Glutamine; Glycine; Hair; Histidine; Humans; Infant; Lysine; Male; Middle Aged; Serine; Skin Diseases; Threonine; Tyrosine; Valine	1968
Inhibition of entry of some amino acids into the brain, with observations on mental retardation in the aminoacidurias. Psychological medicine, 1974, Volume: 4, Issue:3 Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Arginine; Biological Transport, Active; Brain; Caproates; Carbon Radioisotopes; Depression, Chemical; Drug Interactions; Humans; Intellectual Disability; Isoleucine; Keto Acids; Leucine; Rats; Rats, Inbred Strains; Stimulation, Chemical; Threonine	1974
[Methionine toxicity. 5. Amino acid content of blood serum and urine after high doses of methionine and gaseous elimination of 35S from 35S methionine]. Archiv fur Tierernahrung, 1972, Volume: 22, Issue:1 Topics: Administration, Oral; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Glutathione; Glycine; Histidine; Lysine; Methionine; Phenylalanine; Rats; Sulfur Isotopes; Taurine; Threonine; Time Factors; Tyrosine	1972
Amino acid, creatine and creatinine studies in myotonic dystrophy. Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 39, Issue:2 Topics: Adult; Age Factors; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Creatine; Creatinine; Erythrocytes; Female; Glutamine; Glycine; Hemolysis; Humans; Male; Membranes; Middle Aged; Myotonic Dystrophy; Ornithine; Permeability; Serine; Threonine	1972
Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders. The Journal of laboratory and clinical medicine, 1971, Volume: 78, Issue:4 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Aspartic Acid; Biological Transport; Child; Chromatography, Ion Exchange; Cystine; Erythrocytes; Glutamates; Glutathione; Glycine; Histidine; Homocystine; Homocystinuria; Humans; Infant; Maple Syrup Urine Disease; Methionine; Ornithine; Phenylketonurias; Plasma; Renal Tubular Transport, Inborn Errors; Serine; Spectrophotometry; Threonine; Tyrosine	1971
[Endogenous pellagra without hyperaminoaciduria]. Revue neurologique, 1969, Volume: 120, Issue:3 Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Arginine; Chromatography, Paper; Diagnosis, Differential; Electroencephalography; Glutamates; Glutamine; Hartnup Disease; Histidine; Humans; Lysine; Male; Pellagra; Serine; Skin Manifestations; Threonine	1969
Paper chromatographic survey of urinary amino-acids in muscular dystrophy. British medical journal, 1970, Jul-04, Volume: 3, Issue:5713 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Chromatography, Paper; Female; Histidine; Humans; Lysine; Male; Middle Aged; Muscular Dystrophies; Threonine	1970
Vitamin B12-dependent methylmalonicaciduria: amino acid toxicity, long chain ketonuria, and protective effect of vitamin B12. Pediatrics, 1970, Volume: 46, Issue:4 Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Coenzyme A; Diet Therapy; Dietary Proteins; Humans; Isoleucine; Ketones; Leucine; Leukocytes; Male; Malonates; Methionine; Nutritional Requirements; Propionates; Threonine; Valine; Vitamin B 12	1970
[Hyperaminoaciduria in children suffering from progressive muscular dystrophy]. Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1967, Volume: 67, Issue:7 Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Child; Child, Preschool; Creatine; Creatinine; Female; Glutamates; Histidine; Humans; Leucine; Lysine; Male; Methionine; Muscular Dystrophies; Nitrogen; Phenylalanine; Serine; Threonine; Tryptophan; Tyrosine; Valine	1967
Encephalopathy in combination with a new pattern of aminoaciduria. Acta paediatrica Scandinavica, 1969, Volume: 58, Issue:1 Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Central Nervous System; Chromatography; Cyanosis; Dyspnea, Paroxysmal; Electroencephalography; Exchange Transfusion, Whole Blood; Humans; Hyperbilirubinemia; Infant; Infant, Newborn; Infant, Premature, Diseases; Male; Serine; Spectrophotometry; Threonine	1969
Urinary amino acid and peptide excretion patterns in patients with muscular dystrophy (Duchenne). A preliminary study with the autoanalyzer. Clinical chemistry, 1969, Volume: 15, Issue:7 Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Autoanalysis; Child; Child, Preschool; Glutamates; Glycine; Histidine; Humans; Isoleucine; Leucine; Lysine; Male; Muscular Dystrophies; Peptides; Phenylalanine; Serine; Threonine; Tyrosine; Valine	1969