tyrosine has been researched along with Adrenal Hyperplasia, Congenital in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (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 |
|---|---|
| Rass, IT | 1 |
| Kuznetsova, ES; Rass, IT; Zhukovskiĭ, MA | 1 |
| Rigilano, JC; Stevens, MB; Wilson, CC | 1 |
4 other study(ies) available for tyrosine and Adrenal Hyperplasia, Congenital
| Article | Year |
|---|---|
[Blood tyrosine level in glucocorticoid therapy].
Topics: Adrenal Hyperplasia, Congenital; Adult; Child; Glucocorticoids; Humans; Lupus Erythematosus, Systemic; Reference Values; Tyrosine | 1981 |
[Tyrosine content in the blood as an index of the adequacy of glucocorticoid replacement therapy in congenital adrenal cortical dysfunction in children].
Topics: 17-Ketosteroids; Adolescent; Adrenal Hyperplasia, Congenital; Child; Child, Preschool; Female; Glucocorticoids; Humans; Male; Tyrosine | 1979 |
State screening for metabolic disorders in newborns.
Topics: Adrenal Hyperplasia, Congenital; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Biotinidase; Congenital Hypothyroidism; Cystic Fibrosis; Galactosemias; Homocystinuria; Humans; Hypothyroidism; Infant, Newborn; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Tyrosine; United States | 1988 |
Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Metabolism, Inborn Errors; Carrier State; Ceruloplasmin; Cholinesterases; Cystic Fibrosis; Diagnostic Services; Female; Galactosemias; Genetic Diseases, Inborn; Hepatolenticular Degeneration; Humans; Infant; Infant, Newborn; Male; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Phenylketonurias; Porphyrias; Tyrosine; World Health Organization | 1968 |