creatine has been researched along with Fabry Disease in 4 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 a lysosomal storage disorder caused by deficiency of α-galactosidase A, resulting in glycosphingolipid accumulation in organs and tissues, including plasma and urine." | 1.38 | Urinary globotriaosylsphingosine-related biomarkers for Fabry disease targeted by metabolomics. ( Auray-Blais, C; Boutin, M; Clarke, JT; Dupont, FO; Gagnon, R; Lavoie, P, 2012) |
| "Fabry and Gaucher diseases are rare progressive inherited disorders of glycosphingolipid metabolism that affect multiple organ systems." | 1.37 | Magnetic resonance spectroscopy in patients with Fabry and Gaucher disease. ( Bodamer, O; Bogner, W; Gruber, S; Krssak, M; Stadlbauer, A, 2011) |
| "Fabry disease is characterized by accumulation of glycosphingolipids, such as globotriaosylceramide (Gb(3)), in many tissues and body fluids." | 1.36 | How well does urinary lyso-Gb3 function as a biomarker in Fabry disease? ( Auray-Blais, C; Bichet, DG; Casey, R; Clarke, JT; Gagnon, R; Hwu, WL; Keutzer, JM; Millington, DS; Ntwari, A; Oliveira, JP; Sirrs, S; Warnock, DG; West, ML; Young, SP; Zhang, XK, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gruber, S | 1 |
| Bogner, W | 1 |
| Stadlbauer, A | 1 |
| Krssak, M | 1 |
| Bodamer, O | 1 |
| Auray-Blais, C | 2 |
| Ntwari, A | 1 |
| Clarke, JT | 2 |
| Warnock, DG | 1 |
| Oliveira, JP | 1 |
| Young, SP | 1 |
| Millington, DS | 1 |
| Bichet, DG | 1 |
| Sirrs, S | 1 |
| West, ML | 1 |
| Casey, R | 1 |
| Hwu, WL | 1 |
| Keutzer, JM | 1 |
| Zhang, XK | 1 |
| Gagnon, R | 2 |
| Boutin, M | 1 |
| Dupont, FO | 1 |
| Lavoie, P | 1 |
| Politei, JM | 1 |
| Capizzano, AA | 1 |
4 other studies available for creatine and Fabry Disease
| 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 Diseas | 2011 |
How well does urinary lyso-Gb3 function as a biomarker in Fabry disease?
Topics: Adolescent; Adult; Aged; alpha-Galactosidase; Biomarkers; Case-Control Studies; Child; Child, Presch | 2010 |
Urinary globotriaosylsphingosine-related biomarkers for Fabry disease targeted by metabolomics.
Topics: Adolescent; Adult; Aged; Biomarkers; Child; Child, Preschool; Creatine; Data Mining; Fabry Disease; | 2012 |
Magnetic resonance image findings in 5 young patients with Fabry disease.
Topics: Adolescent; Adult; Aspartic Acid; Brain; Brain Chemistry; Creatine; Diffusion Magnetic Resonance Ima | 2006 |