tyrosine has been researched along with Cystinuria in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 17 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| TOMPSETT, SL | 1 |
| Efron, ML | 1 |
| Reavey, PC; Yadav, GC | 1 |
| Ghobrial, HK; Meihak, L; O'Brien, TD; Osborne, CA; Stevens, JB | 1 |
| Jackson, SH | 1 |
| Bundgaard, L; Winther, A | 1 |
| Farrelly, RO; Watkins, WB | 1 |
| Holmgren, G; Nordström, S; Thorburn, W | 1 |
| Ampola, MG | 1 |
| Levy, HL | 1 |
| Tomaszewski, L | 1 |
| Lohrenz, FN; Tewksbury, DA | 1 |
| Bunting, R; Diamond, S; Hansen, S; Perry, TL; Tischler, B; Weppler, VC | 1 |
| Matthews, DM | 1 |
| Mawer, GE; Nixon, E | 1 |
| Abdel Kader, MM; Abdel Wahab, F; Ata, AA; Emara, SH; Soliman, L | 1 |
2 review(s) available for tyrosine and Cystinuria
| Article | Year |
|---|---|
Phenylketonuria and other disorders of amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Counseling; Cystathionine; Cystinosis; Cystinuria; Diet Therapy; Dietary Proteins; Family; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Hyperglycemia; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Ornithine; Phenylketonurias; Pregnancy; Proline; Tyrosine | 1973 |
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 |
15 other study(ies) available for tyrosine and Cystinuria
| Article | Year |
|---|---|
The use of a cation-exchange resin in the determination of some basic substances (tyrosine, tyramine, kynurenine, 3-hydroxykynurenine and cystine) in urine.
Topics: Body Fluids; Cations; Cystinuria; Humans; Ion Exchange Resins; Kynurenine; Tyramine; Tyrosine | 1962 |
Diet therapy for inborn errors of amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child, Preschool; Coenzymes; Cystinuria; Diet Therapy; Hartnup Disease; Humans; Infant; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Tyrosine | 1967 |
Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.
Topics: Amino Acid Metabolism, Inborn Errors; Argininosuccinic Acid; Australia; Cystinuria; Ethnicity; Europe; Galactosemias; Genetics, Population; Hartnup Disease; Histidine; Homocystinuria; Humans; Inbreeding; Infant, Newborn; Israel; Japan; Maple Syrup Urine Disease; Mass Screening; New Zealand; North America; Phenylketonurias; Tyrosine | 1975 |
Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Citrulline; Cystinuria; Female; Glycine; Homocystinuria; Humans; Infant; Infant, Newborn; Kuwait; Male; Maple Syrup Urine Disease; Phenylalanine; Phenylketonurias; Proline; Tyrosine | 1988 |
Crystalluria. Observations, interpretations, and misinterpretations.
Topics: Animals; Bilirubin; Calcium Carbonate; Calcium Oxalate; Calcium Phosphates; Cholesterol; Crystallography; Cystinuria; Dog Diseases; Dogs; Hippurates; Leucine; Magnesium; Magnesium Compounds; Minerals; Phosphates; Quaternary Ammonium Compounds; Struvite; Tyrosine; Uric Acid; Urinary Calculi | 1986 |
Problems in screening infants for defects of amino acid metabolism.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Chromatography, Thin Layer; Color; Cystinuria; Evaluation Studies as Topic; Humans; Indicators and Reagents; Infant; Infant, Newborn; Infant, Premature; Mass Screening; Phenylketonurias; Rickets; Staining and Labeling; Tyrosine | 1973 |
Argininosuccinic aciduria in hereditary hair diseases.
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 |
Screening for disorders of amino acid metabolism by thin-layer high voltage electrophoresis.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Analgesics; Anti-Inflammatory Agents; Chromatography, Thin Layer; Cystinuria; Electrophoresis; Humans; Hydrogen-Ion Concentration; Indicators and Reagents; Indoles; Mass Screening; Membranes; Methods; Phenylketonurias; Silicon Dioxide; Sulfates; Tyrosine | 1968 |
Urinary metabolic studies in hereditary macular degeneration.
Topics: Albuminuria; Amino Acids; Carbohydrates; Cystinuria; Electrophoresis, Paper; Female; Glycosuria; Histidine; Humans; Keto Acids; Male; Pedigree; Phenylketonurias; Retinal Degeneration; Syndrome; Tyrosine | 1974 |
[The inborn errors of metabolism of amino acids].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chemical Phenomena; Chemistry; Cystinuria; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Sarcosine; Tyrosine; Valine | 1973 |
Circadian ythm of human urinary amino acid excretion in fed and fasted states.
Topics: 17-Hydroxycorticosteroids; Adult; Alanine; Amino Acids; Asparagine; Circadian Rhythm; Cystinuria; Fasting; Feeding Behavior; Glutamates; Glutamine; Glycine; Humans; Male; Middle Aged; Phenylalanine; Serine; Threonine; Tyrosine; Valine | 1970 |
Unrecognized maternal biochemical disease: an uncommon cause of mental retardation in children.
Topics: Child; Cystinuria; Female; Glycine; Humans; Infant, Newborn; Intellectual Disability; Lysine; Metabolic Diseases; Phenylalanine; Phenylketonurias; Pregnancy; Proline; Tyrosine | 1970 |
Experimental approach in chemical pathology.
Topics: Adult; Amblyopia; Animals; Biological Transport; Cystinuria; Dipeptides; Female; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Metabolic Diseases; Metabolism, Inborn Errors; Methionine; Nitrogen; Peptides; Proteins; Smoking; Tyrosine; Vitamin B 12 | 1971 |
The net absorption of the amino acid constituents of a protein meal in normal and cystinuric subjects.
Topics: Adult; Amino Acids; Arginine; Cystine; Cystinuria; Dietary Proteins; Female; Glycols; Humans; Indicators and Reagents; Intestinal Absorption; Lysine; Male; Phenylalanine; Tyrosine | 1969 |
Urinary amino acid patterns in simple and complicated bilharziasis.
Topics: Adolescent; Adult; Aged; Alanine; Amino Acids; Ascites; Chromatography, Paper; Cystinuria; Hepatomegaly; Humans; Liver Diseases; Male; Middle Aged; Schistosomiasis; Splenomegaly; Threonine; Tryptophan; Tyrosine | 1969 |