glycine has been researched along with Anterior Fascicular Block in 1 studies
Excerpt | Relevance | Reference |
---|---|---|
"Fabry disease is an X-linked lysosomal storage disorder caused by mutations of the α-galactosidase A gene (GLA), and the disease is a relatively prevalent cause of left ventricular hypertrophy mimicking idiopathic hypertrophic cardiomyopathy." | 1.37 | Clinical and genetic investigation of a Japanese family with cardiac fabry disease. Identification of a novel α-galactosidase A missense mutation (G195V). ( 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, 2011) |
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 | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Nakagawa, N | 1 |
Maruyama, H | 1 |
Ishihara, T | 1 |
Seino, U | 1 |
Kawabe, J | 1 |
Takahashi, F | 1 |
Kobayashi, M | 1 |
Yamauchi, A | 1 |
Sasaki, Y | 1 |
Sakamoto, N | 1 |
Ota, H | 1 |
Tanabe, Y | 1 |
Takeuchi, T | 1 |
Takenaka, T | 1 |
Kikuchi, K | 1 |
Hasebe, N | 1 |
1 other study available for glycine and Anterior Fascicular Block
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; Coro | 2011 |