aspartic acid has been researched along with alpha-Galactosidase A Deficiency in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bodamer, O; Bogner, W; Gruber, S; Krssak, M; Stadlbauer, A | 1 |
| Endreffy, E; László, A; Morvai, L; Raffai, S; Sallay, E; Török, E; Török, L; van Amstel, JK | 1 |
| Capizzano, AA; Politei, JM | 1 |
| Battaglini, M; Borsini, W; Bramanti, P; Buchner, S; De Stefano, N; Federico, A; Giorgio, A; Marino, S; Mortilla, M; Stromillo, ML | 1 |
| Becker, C; Gehler, J; Hartmann, J; Sewell, AC; Spranger, J | 1 |
5 other study(ies) available for aspartic acid and alpha-Galactosidase A Deficiency
| Article | Year |
|---|---|
Magnetic resonance spectroscopy in patients with Fabry and Gaucher disease.
Topics: Adult; Aspartic Acid; Case-Control Studies; Choline; Creatine; Fabry Disease; Female; Gaucher Disease; Humans; Inositol; Magnetic Resonance Spectroscopy; Male; Middle Aged | 2011 |
Mutation analysis of alpha-galactosidase a gene in Hungarian Fabry patients.
Topics: Adult; alpha-Galactosidase; Aspartic Acid; Codon; DNA Mutational Analysis; Exons; Fabry Disease; Humans; Male; Mutation, Missense; Polymerase Chain Reaction; Tyrosine | 2012 |
Magnetic resonance image findings in 5 young patients with Fabry disease.
Topics: Adolescent; Adult; Aspartic Acid; Brain; Brain Chemistry; Creatine; Diffusion Magnetic Resonance Imaging; Echo-Planar Imaging; Fabry Disease; Female; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Middle Aged | 2006 |
Diffuse structural and metabolic brain changes in Fabry disease.
Topics: Adult; alpha-Galactosidase; Aspartic Acid; Axons; Brain; Brain Chemistry; Disease Progression; DNA; Fabry Disease; Female; Heterozygote; Homozygote; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Middle Aged; Mutation | 2006 |
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family.
Topics: Abnormalities, Multiple; Acetylglucosamine; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Fabry Disease; Facial Bones; Female; Glucosamine; Humans; Intellectual Disability; Italy; Male; Pedigree; Skull | 1981 |