threonine has been researched along with Angioedema, Hereditary, Type III 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 | 0 (0.00) | 29.6817 |
2010's | 2 (100.00) | 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 |
Baeza, ML; Prieto, A; Rodríguez-Marco, A; Rodríguez-Sainz, C; Rubio, M; Zubeldia, JM | 1 |
2 other study(ies) available for threonine and Angioedema, Hereditary, Type III
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 |
Factor XII gene missense mutation Thr328Lys in an Arab family with hereditary angioedema type III.
Topics: Adolescent; Adult; Arabs; Factor XII; Family; Female; Hereditary Angioedema Type III; Humans; Lysine; Male; Morocco; Mutation, Missense; Pedigree; Threonine | 2011 |