glycine has been researched along with Fabry Disease in 1 studies
Fabry Disease: An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders.
| 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 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; Coro | 2011 |