histidine has been researched along with Congenital Hypothyroidism in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 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 | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Hasegawa, T; Kashimada, K; Narumi, S; Ono, M; Sugisawa, C | 1 |
| Brown, DA; Connelly, J; Francis, I; Hill, G; Masters, P; McFarlane, J; Pitt, D; Raby, J; Tucker, RG; Wilcken, B | 1 |
| Mamunes, P | 1 |
1 review(s) available for histidine and Congenital Hypothyroidism
| Article | Year |
|---|---|
Newborn screening for metabolic disorders.
Topics: Chromatography, Paper; Congenital Hypothyroidism; Cost-Benefit Analysis; Costs and Cost Analysis; Female; Fluorometry; Galactosemias; Histidine; Humans; Hypothyroidism; Infant, Newborn; Infant, Newborn, Diseases; Metabolism, Inborn Errors; Phenylketonurias; Pregnancy; Time Factors; United States; UTP-Hexose-1-Phosphate Uridylyltransferase | 1976 |
2 other study(ies) available for histidine and Congenital Hypothyroidism
| Article | Year |
|---|---|
Inactivation of a Frameshift TSH Receptor Variant Val711Phefs*18 is Due to Acquisition of a Hydrophobic Degron.
Topics: Amino Acid Substitution; Arginine; Child, Preschool; Congenital Hypothyroidism; DNA Mutational Analysis; Frameshift Mutation; HEK293 Cells; Histidine; Humans; Hydrophobic and Hydrophilic Interactions; Male; Parents; Pedigree; Phenylalanine; Protein Domains; Protein Stability; Proteolysis; Receptors, Thyrotropin; Valine | 2021 |
Genetic screening of the newborn in Australia. Results for 1978.
Topics: Australia; Blood Stains; Congenital Hypothyroidism; Cystinuria; Female; Fetal Blood; Genetic Testing; Histidine; Homocystinuria; Humans; Hypothyroidism; Infant, Newborn; Infant, Newborn, Diseases; Male; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias | 1979 |