histidine has been researched along with homocystine in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 6 (85.71) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Enzenauer, J; Matz, D; Menne, F | 1 |
Spray, GH; Williams, DL | 1 |
Levy, HL | 1 |
Kang, AH; Trelstad, RL | 1 |
Barkin, E; Levy, HL | 1 |
Abbott, EH; Martell, AE | 1 |
Aoki, K | 1 |
2 review(s) available for histidine and homocystine
Article | Year |
---|---|
Genetic screening.
Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine | 1973 |
[Disorders of amino acids].
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Female; Histidine; Homocystine; Humans; Infant; Japan; Male; Maple Syrup Urine Disease; Phenylalanine; Reference Standards | 1993 |
5 other study(ies) available for histidine and homocystine
Article | Year |
---|---|
[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 |
The effects of dietary histidine, methionine and homocystine on vitamin B12 and folate levels in rat liver.
Topics: Animals; Body Weight; Female; Folic Acid; Histidine; Homocystine; Liver; Male; Methionine; Proteins; Rats; Vitamin B 12; Vitamin B 12 Deficiency | 1976 |
A collagen defect in homocystinuria.
Topics: Adult; Aldehydes; Amino Acids; Biopsy; Borohydrides; Child; Collagen; Dialysis; Histidine; Homocysteine; Homocystine; Homocystinuria; Humans; Hydrolysis; Hydroxylysine; Methionine; Microscopy, Electron; Norleucine; Skin; Sodium; Solubility; Temperature; Time Factors; Tritium | 1973 |
Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
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 |
Pyridoxine and pyridoxal analogs. 13. A nuclear magnetic resonance study of the condensation of polyfunctional amino acids with pyridoxal.
Topics: Amino Acids; Chemical Phenomena; Chemistry; Cycloserine; Histidine; Homocysteine; Homocystine; Imidazoles; Magnetic Resonance Spectroscopy; Pyridoxal Phosphate; Serine; Threonine | 1970 |