isoleucine has been researched along with Adult-Onset Dystonias in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Funayama, M; Hasegawa, K; Ichinose, H; Obata, F; Ohta, E; Toyoshima, I | 1 |
Funayama, M; Hasegawa, K; Ichinose, H; Maeda, K; Matsuo, M; Obata, F; Ohta, E; Shimazu, H; Tomoko, N; Toyoshima, I; Urano, F; Yokoyama, H; Yoshino, S; Yukihiko, K | 1 |
Chung, SJ; Ko, TS; Yoo, HW; Yum, MS | 1 |
3 other study(ies) available for isoleucine and Adult-Onset Dystonias
Article | Year |
---|---|
A new mutation (Thr106Ile) of the GTP cyclohydrolase 1 gene associated with DYT5 dystonia (Segawa disease).
Topics: Adult; Child; DNA Mutational Analysis; Dystonic Disorders; Exons; Female; GTP Cyclohydrolase; Humans; Isoleucine; Mutation; Threonine | 2005 |
Novel mutations in the guanosine triphosphate cyclohydrolase 1 gene associated with DYT5 dystonia.
Topics: Adolescent; Adult; Animals; Biopterins; Child; Child, Preschool; DNA Mutational Analysis; Dystonic Disorders; Exons; Female; GTP Cyclohydrolase; Humans; Isoleucine; Japan; Male; Microsatellite Repeats; Mutation; Neopterin; Threonine | 2006 |
Autosomal-dominant guanosine triphosphate cyclohydrolase I deficiency with novel mutations.
Topics: Child; DNA Mutational Analysis; Dystonic Disorders; Female; GTP Cyclohydrolase; Humans; Isoleucine; Korea; Male; Mutation; Threonine | 2008 |