valine has been researched along with Fabry Disease in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hasebe, N; Ishihara, T; Kawabe, J; Kikuchi, K; Kobayashi, M; Maruyama, H; Nakagawa, N; Ota, H; Sakamoto, N; Sasaki, Y; Seino, U; Takahashi, F; Takenaka, T; Takeuchi, T; Tanabe, Y; Yamauchi, A | 1 |
| Ishii, S; Itoh, K; Kamei, S; Kase, R; Kawamura, O; Okumiya, T; Sakuraba, H | 1 |
2 other study(ies) available for valine and Fabry Disease
| Article | Year |
|---|---|
Clinical and genetic investigation of a Japanese family with cardiac fabry disease. Identification of a novel α-galactosidase A missense mutation (G195V).
Topics: Adult; alpha-Galactosidase; Amino Acid Substitution; Bundle-Branch Block; Coronary Angiography; Coronary Vasospasm; DNA Mutational Analysis; Echocardiography; Electrocardiography; Exons; Fabry Disease; Female; Genotype; Glycine; Humans; Hypertrophy, Left Ventricular; Japan; Magnetic Resonance Imaging; Male; Microscopy, Electron; Middle Aged; Mutation, Missense; Myocardium; Natriuretic Peptide, Brain; Pedigree; Peptide Fragments; Signal Processing, Computer-Assisted; Valine; Young Adult | 2011 |
Novel missense mutation (M72V) of alpha-galactosidase gene and its expression product in an atypical Fabry hemizygote.
Topics: Adult; alpha-Galactosidase; Amino Acid Substitution; Animals; COS Cells; DNA; DNA Mutational Analysis; Fabry Disease; Gene Expression Regulation, Enzymologic; Heterozygote; Humans; Male; Methionine; Mutation, Missense; Point Mutation; Valine | 1998 |