valine has been researched along with Budd-Chiari Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Handa, H; Karasawa, M; Koiso, H; Miyawaki, S; Murakami, H; Nojima, Y; Saitoh, T; Sato, K; Takagi, H; Toyama, K; Tsukamoto, N; Uchiumi, H; Yamane, A; Yokohama, A | 1 |
1 other study(ies) available for valine and Budd-Chiari Syndrome
Article | Year |
---|---|
Low burden of a JAK2-V617F mutated clone in monoclonal haematopoiesis in a Japanese woman with Budd-Chiari syndrome.
Topics: Adult; Asian People; Base Sequence; Budd-Chiari Syndrome; DNA; Female; Genome, Human; Hematopoiesis; Humans; Janus Kinase 2; Mutation; Phenylalanine; RNA; Tomography, X-Ray Computed; Valine; X Chromosome Inactivation | 2009 |