threonine has been researched along with Angioedema, Hereditary in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Caballero, T; Drouet, C; Favier, B; Gómez-Traseira, C; López-Lera, A; López-Trascasa, M; Pérez-Fernández, E; Prior, N | 1 |
| Fernández-Cruz, E; Prieto, A; Rodriguez-Sainz, C; Rubio, M; Tornero, P | 1 |
2 other study(ies) available for threonine and Angioedema, Hereditary
| Article | Year |
|---|---|
Hereditary angioedema caused by the p.Thr309Lys mutation in the F12 gene: a multifactorial disease.
Topics: Adolescent; Adult; Angioedemas, Hereditary; Factor XII; Family; Female; Hereditary Angioedema Type III; Humans; Lysine; Male; Mutation; Pedigree; Severity of Illness Index; Spain; Threonine; Young Adult | 2013 |
Missense mutation Thr309Lys in the coagulation factor XII gene in a Spanish family with hereditary angioedema type III.
Topics: Adult; Amino Acid Substitution; Angioedemas, Hereditary; Factor XII; Female; Humans; Lysine; Male; Mutation, Missense; Pedigree; Threonine | 2009 |