tyrosine has been researched along with Autosomal Chromosome Disorders in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (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 |
|---|---|
| Gallasch, G; Jaeger, W; Lutz, P; Schmidt, H; Schnyder, UW | 1 |
| Finegold, MJ | 1 |
| Jones, B; Jones, JE; Lizarralde, G; Seal, US | 1 |
| van der Horst, JL; Wadman, SK | 1 |
| Hansen, S; Hardwick, DF; Perry, TL; Pohlmann, L; Warrington, PD | 1 |
1 review(s) available for tyrosine and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Cholestatic syndromes in infancy.
Topics: Anemia, Hemolytic; Bile; Bile Ducts; Cholestasis; Chromosome Aberrations; Chromosome Disorders; Fasting; Fructose Intolerance; Galactosemias; Histiocytosis, Langerhans-Cell; Humans; Infant; Infant, Newborn; Infections; Jaundice, Neonatal; Liver; Liver Cirrhosis; Niemann-Pick Diseases; Nutritional Physiological Phenomena; Syndrome; Tyrosine | 1976 |
4 other study(ies) available for tyrosine and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
[Tyrosinemia and Richner-Hanhart syndrome (an autosomal recessive hereditary metabolic disease of childhood with bilateral dendritic pseudokeratitis, keratosis palmaris et plantaris and mental deficiency)].
Topics: Amino Acid Metabolism, Inborn Errors; Child; Chromosome Aberrations; Chromosome Disorders; Genes, Recessive; Humans; Intellectual Disability; Keratitis, Dendritic; Keratoderma, Palmoplantar; Syndrome; Tyrosine | 1978 |
Goitrous cretinism with chromosomal aberration and defect in thyroglobulin synthesis.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Chromatography, Gel; Chromosome Aberrations; Chromosome Disorders; Congenital Hypothyroidism; Diiodotyrosine; Goiter; Humans; Immunodiffusion; Iodine Radioisotopes; Male; Mosaicism; Thyroglobulin; Thyroid Function Tests; Thyroxine; Triiodothyronine; Tyrosine; Ultracentrifugation | 1966 |
A variant form of branched-chain keto aciduria.
Topics: Amino Acids; Child Behavior Disorders; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Diet Therapy; Dietary Proteins; Female; Heterozygote; Humans; Infant; Intellectual Disability; Isoleucine; Keto Acids; Leucine; Male; Maple Syrup Urine Disease; Methionine; Motor Skills; Pedigree; Phenylketonurias; Tyrosine; Valine | 1971 |
Methionine induction of experimental tyrosinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Chromosome Aberrations; Chromosome Disorders; Guinea Pigs; Methionine; Pancreas; Tyrosine | 1967 |