Page last updated: 2024-10-17

creatine and alpha-Galactosidase A Deficiency

creatine has been researched along with alpha-Galactosidase A Deficiency in 4 studies

Research Excerpts

ExcerptRelevanceReference
"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."1.38Urinary 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."1.37Magnetic 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."1.36How 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)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gruber, S1
Bogner, W1
Stadlbauer, A1
Krssak, M1
Bodamer, O1
Auray-Blais, C2
Ntwari, A1
Clarke, JT2
Warnock, DG1
Oliveira, JP1
Young, SP1
Millington, DS1
Bichet, DG1
Sirrs, S1
West, ML1
Casey, R1
Hwu, WL1
Keutzer, JM1
Zhang, XK1
Gagnon, R2
Boutin, M1
Dupont, FO1
Lavoie, P1
Politei, JM1
Capizzano, AA1

Other Studies

4 other studies available for creatine and alpha-Galactosidase A Deficiency

ArticleYear
Magnetic resonance spectroscopy in patients with Fabry and Gaucher disease.
    European journal of radiology, 2011, Volume: 79, Issue:2

    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?
    Clinica chimica acta; international journal of clinical chemistry, 2010, Dec-14, Volume: 411, Issue:23-24

    Topics: Adolescent; Adult; Aged; alpha-Galactosidase; Biomarkers; Case-Control Studies; Child; Child, Presch

2010
Urinary globotriaosylsphingosine-related biomarkers for Fabry disease targeted by metabolomics.
    Analytical chemistry, 2012, Mar-20, Volume: 84, Issue:6

    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.
    The neurologist, 2006, Volume: 12, Issue:2

    Topics: Adolescent; Adult; Aspartic Acid; Brain; Brain Chemistry; Creatine; Diffusion Magnetic Resonance Ima

2006