valine and Fabry Disease

valine has been researched along with Fabry Disease in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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, A1
Ishii, S; Itoh, K; Kamei, S; Kase, R; Kawamura, O; Okumiya, T; Sakuraba, H1

Other Studies

2 other study(ies) available for valine and Fabry Disease

ArticleYear
Clinical and genetic investigation of a Japanese family with cardiac fabry disease. Identification of a novel α-galactosidase A missense mutation (G195V).
    International heart journal, 2011, Volume: 52, Issue:5

    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.
    Human mutation, 1998, Volume: Suppl 1

    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