methionine has been researched along with Fabry Disease in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akai, Y; Doi, K; Kodama, T; Mitobe, S; Noiri, E; Ohno, K; Saito, S; Saito, Y; Sakuraba, H; Takenaka, T; Tanaka, T; Togawa, T; Tsukimura, T; Yoshino, M | 1 |
| Fervenza, FC; Lager, D; Lai, LW; Leung, N; Lien, YH; Rosenthal, D; Shang, S | 1 |
| Ishii, S; Itoh, K; Kamei, S; Kase, R; Kawamura, O; Okumiya, T; Sakuraba, H | 1 |
3 other study(ies) available for methionine and Fabry Disease
| Article | Year |
|---|---|
Mutant α-galactosidase A with M296I does not cause elevation of the plasma globotriaosylsphingosine level.
Topics: Adult; alpha-Galactosidase; Amino Acid Substitution; Asian People; Biomarkers; Child; Child, Preschool; Fabry Disease; Female; Glycolipids; Humans; Isoleucine; Male; Methionine; Middle Aged; Mutation; Phenotype; Sphingolipids | 2012 |
A novel alpha-galactosidase a mutant (M42L) identified in a renal variant of Fabry disease.
Topics: Aged; alpha-Galactosidase; Amino Acid Substitution; Fabry Disease; Genetic Variation; Humans; Leucine; Male; Methionine; Mutation, Missense | 2004 |
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 |