methionine has been researched along with Classic Galactosemia in 14 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (50.00) | 18.7374 |
| 1990's | 2 (14.29) | 18.2507 |
| 2000's | 2 (14.29) | 29.6817 |
| 2010's | 2 (14.29) | 24.3611 |
| 2020's | 1 (7.14) | 2.80 |
| Authors | Studies |
|---|---|
| Li, D; Li, X; Liu, J; Xiao, M; Xie, Z; Zhang, Q; Zhang, Y; Zhang, Z | 1 |
| Huang, M; McAuley, M; Timson, DJ | 1 |
| Hong, SP; Kwon, HJ; Lee, JY; Lee, YM; Sim, HJ; Yoon, HR | 1 |
| Paunier, L | 1 |
| Christacos, NC; Fridovich-Keil, JL; Harreman, MT; Wohlers, TM | 1 |
| Fridovich-Keil, JL; Wohlers, TM | 1 |
| Angelicheva, D; Hunter, M; Kalaydjieva, L; Levy, HL; Pueschel, SM | 1 |
| Enzenauer, J; Matz, D; Menne, F | 1 |
| Di Giamberardino, L; Figliomeni, B; Filliatreau, G; Hassig, R; Tomlinson, DR; Willars, GB | 1 |
| Chaplain, TL; Meakem, T; Williams, EH | 1 |
| Donnell, GN; Koch, R; Lieberman, E; Shaw, KN | 1 |
| Royer, P | 1 |
| Alpers, DH; Thier, SO | 1 |
| Collombel, C; Cotte, J; David, M; Dutruge, J; Jeune, M; Michel, M | 1 |
1 review(s) available for methionine and Classic Galactosemia
| Article | Year |
|---|---|
Disorders of intestinal transport of amino acids.
Topics: Amino Acids; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Fructose; Galactosemias; Genes, Recessive; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Lysine; Methionine; Phenylketonurias; Proline; Renal Tubular Transport, Inborn Errors; Tryptophan | 1969 |
13 other study(ies) available for methionine and Classic Galactosemia
| Article | Year |
|---|---|
[Clinical characteristics and genetic analysis of a child with Galactosemia due to compound heterozygous variants of GALT gene].
Topics: Child; Female; Galactosemias; Genetic Testing; Health Status; Humans; Methionine; Muscle Hypotonia; Mutation | 2023 |
Insight into the mechanism of galactokinase: Role of a critical glutamate residue and helix/coil transitions.
Topics: Adenosine Triphosphate; Aspartic Acid; Catalysis; Catalytic Domain; Galactokinase; Galactose; Galactosemias; Glutamic Acid; Humans; Methionine; Molecular Dynamics Simulation; Protein Conformation; Substrate Specificity | 2017 |
Methionine/galactose ratio on newborn blood spots useful for reduction of false positives for homocystinuria and galactosemia by high-performance anion-exchange chromatography with pulsed amperometric detection.
Topics: Anion Exchange Resins; Chromatography, High Pressure Liquid; Chromatography, Ion Exchange; Electrochemistry; False Positive Reactions; Galactose; Galactosemias; Homocystinuria; Humans; Infant, Newborn; Methionine; Neonatal Screening; Reproducibility of Results | 2012 |
[Detections tests for newborn infants].
Topics: Amino Acid Metabolism, Inborn Errors; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Methionine; Phenylalanine | 1981 |
Identification and characterization of a mutation, in the human UDP-galactose-4-epimerase gene, associated with generalized epimerase-deficiency galactosemia.
Topics: Alleles; Amino Acid Substitution; Enzyme Stability; Female; Galactosemias; Gene Expression Regulation; Homozygote; Humans; Male; Methionine; Mutation; NAD; Pedigree; UDPglucose 4-Epimerase; Uridine Diphosphate N-Acetylgalactosamine; Valine; Yeasts | 1999 |
Studies of the V94M-substituted human UDPgalactose-4-epimerase enzyme associated with generalized epimerase-deficiency galactosaemia.
Topics: Amino Acid Substitution; Galactose; Galactosemias; Galactosephosphates; Gene Expression; Humans; Kinetics; Methionine; Saccharomyces cerevisiae; UDPglucose 4-Epimerase; Uridine Diphosphate N-Acetylgalactosamine; Valine | 2000 |
Novel mutations in the GALK1 gene in patients with galactokinase deficiency.
Topics: Adolescent; Adult; Alanine; Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; Child, Preschool; Cysteine; Female; Galactokinase; Galactosemias; Humans; Male; Methionine; Mice; Molecular Sequence Data; Mutation; Proline; Sequence Deletion; Threonine | 2001 |
[Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2].
Topics: Acute Disease; Diagnosis, Differential; Galactose; Galactosemias; Germany, West; Histidine; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Methionine; Phosphotransferases | 1976 |
Proteins of slow axonal transport in sciatic motoneurones of rats with streptozotocin-induced diabetes or galactosaemia.
Topics: Animals; Autoradiography; Axonal Transport; Carbohydrates; Diabetes Mellitus, Experimental; Electrophoresis, Polyacrylamide Gel; Galactosemias; Inositol; Male; Methionine; Molecular Weight; Motor Neurons; Nerve Tissue Proteins; Rats; Rats, Inbred Strains; Reference Values; Sciatic Nerve; Sulfur Radioisotopes; Tubulin | 1990 |
A temporal and spatial study of the synthesis and degradation of water-soluble and insoluble proteins in galactosemic rat lenses.
Topics: Animals; Autoradiography; Cataract; Crystallins; Electrophoresis, Polyacrylamide Gel; Female; Galactose; Galactosemias; Methionine; Rats; Rats, Inbred Strains; Solubility; Time Factors | 1985 |
Cystathioninuria.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carcinoma, Hepatocellular; Child, Preschool; Cysteine; Diet Therapy; Female; Galactosemias; Glycogen; Humans; Infant; Intellectual Disability; Liver Neoplasms; Male; Maple Syrup Urine Disease; Methionine; Middle Aged; Neuroblastoma; Phenylketonurias; Portal Vein; Pyridoxine; Serine; Sulfisoxazole; Tyrosine | 1967 |
[Dietetics in hereditary enzyme deficiencies].
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Diarrhea, Infantile; Diet Therapy; Galactosemias; Homocystinuria; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Phenylalanine; Phenylketonurias; Tyrosine; Valine | 1970 |
[Transient hypertyrosinemia secondary to hepatic involvement. 2 cases of different etiologies (galactosemia, hepatitis)].
Topics: Female; Galactosemias; Hepatitis; Humans; Infant; Infant, Newborn; Liver Diseases; Male; Methionine; Tyrosine | 1970 |