BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 19259782)

  • 1. Leukocyte perturbation associated with Fabry disease.
    Rozenfeld P; Agriello E; De Francesco N; Martinez P; Fossati C
    J Inherit Metab Dis; 2009 Dec; 32 Suppl 1():S67-77. PubMed ID: 19259782
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Reduced glucosylceramide in the mouse model of Fabry disease: correction by successful enzyme replacement therapy.
    Quinta R; Rodrigues D; Assunção M; Macedo MF; Azevedo O; Cunha D; Oliveira P; Sá Miranda MC
    Gene; 2014 Feb; 536(1):97-104. PubMed ID: 24334116
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Efficacy and safety of enzyme-replacement-therapy with agalsidase alfa in 36 treatment-naïve Fabry disease patients.
    Tsuboi K; Yamamoto H
    BMC Pharmacol Toxicol; 2017 Jun; 18(1):43. PubMed ID: 28592315
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of globotriaosylceramide (Gb
    Toupin A; Lavoie P; Arthus MF; Abaoui M; Boutin M; Fortier C; Ménard C; Bichet DG; Auray-Blais C
    Anal Chim Acta; 2018 Jul; 1015():35-49. PubMed ID: 29530250
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fabry disease peripheral blood immune cells release inflammatory cytokines: role of globotriaosylceramide.
    De Francesco PN; Mucci JM; Ceci R; Fossati CA; Rozenfeld PA
    Mol Genet Metab; 2013 May; 109(1):93-9. PubMed ID: 23452955
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Plasma globotriaosylsphingosine as a biomarker of Fabry disease.
    Togawa T; Kodama T; Suzuki T; Sugawara K; Tsukimura T; Ohashi T; Ishige N; Suzuki K; Kitagawa T; Sakuraba H
    Mol Genet Metab; 2010 Jul; 100(3):257-61. PubMed ID: 20409739
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M).
    Pereira EM; Silva ASD; Silva RND; Monte Neto JT; Nascimento FFD; Sousa JLM; Costa Filho HCSAL; Sales Filho HLA; Labilloy A; Monte SJHD
    J Bras Nefrol; 2018; 40(4):333-338. PubMed ID: 29927462
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Low-dose agalsidase beta treatment in male pediatric patients with Fabry disease: A 5-year randomized controlled trial.
    Ramaswami U; Bichet DG; Clarke LA; Dostalova G; Fainboim A; Fellgiebel A; Forcelini CM; An Haack K; Hopkin RJ; Mauer M; Najafian B; Scott CR; Shankar SP; Thurberg BL; Tøndel C; Tylki-Szymanska A; Bénichou B; Wijburg FA
    Mol Genet Metab; 2019 May; 127(1):86-94. PubMed ID: 30987917
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease.
    Schiffmann R; Murray GJ; Treco D; Daniel P; Sellos-Moura M; Myers M; Quirk JM; Zirzow GC; Borowski M; Loveday K; Anderson T; Gillespie F; Oliver KL; Jeffries NO; Doo E; Liang TJ; Kreps C; Gunter K; Frei K; Crutchfield K; Selden RF; Brady RO
    Proc Natl Acad Sci U S A; 2000 Jan; 97(1):365-70. PubMed ID: 10618424
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Effects of enzyme replacement therapy on the cardiomyopathy of Anderson-Fabry disease: a randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa.
    Hughes DA; Elliott PM; Shah J; Zuckerman J; Coghlan G; Brookes J; Mehta AB
    Heart; 2008 Feb; 94(2):153-8. PubMed ID: 17483124
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Globotriaosylceramide is correlated with oxidative stress and inflammation in Fabry patients treated with enzyme replacement therapy.
    Biancini GB; Vanzin CS; Rodrigues DB; Deon M; Ribas GS; Barschak AG; Manfredini V; Netto CB; Jardim LB; Giugliani R; Vargas CR
    Biochim Biophys Acta; 2012 Feb; 1822(2):226-32. PubMed ID: 22085605
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Enzyme replacement therapy stabilizes obstructive pulmonary Fabry disease associated with respiratory globotriaosylceramide storage.
    Wang RY; Abe JT; Cohen AH; Wilcox WR
    J Inherit Metab Dis; 2008 Dec; 31 Suppl 2():S369-74. PubMed ID: 18937048
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Higher apoptotic state in Fabry disease peripheral blood mononuclear cells.: effect of globotriaosylceramide.
    De Francesco PN; Mucci JM; Ceci R; Fossati CA; Rozenfeld PA
    Mol Genet Metab; 2011 Nov; 104(3):319-24. PubMed ID: 21724436
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Surges in proteinuria are associated with plasma GL-3 elevations in a young patient with classic Fabry disease.
    Kanai T; Ito T; Odaka J; Saito T; Aoyagi J; Betsui H; Yamagata T
    Eur J Pediatr; 2016 Mar; 175(3):427-31. PubMed ID: 26454753
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Is globotriaosylceramide a useful biomarker in Fabry disease?
    Young E; Mills K; Morris P; Vellodi A; Lee P; Waldek S; Winchester B
    Acta Paediatr Suppl; 2005 Mar; 94(447):51-4; discussion 37-8. PubMed ID: 15895713
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Treatment of neutral glycosphingolipid lysosomal storage diseases via inhibition of the ABC drug transporter, MDR1. Cyclosporin A can lower serum and liver globotriaosyl ceramide levels in the Fabry mouse model.
    Mattocks M; Bagovich M; De Rosa M; Bond S; Binnington B; Rasaiah VI; Medin J; Lingwood C
    FEBS J; 2006 May; 273(9):2064-75. PubMed ID: 16724420
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levels.
    Vedder AC; Linthorst GE; van Breemen MJ; Groener JE; Bemelman FJ; Strijland A; Mannens MM; Aerts JM; Hollak CE
    J Inherit Metab Dis; 2007 Feb; 30(1):68-78. PubMed ID: 17206462
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease.
    Eng CM; Guffon N; Wilcox WR; Germain DP; Lee P; Waldek S; Caplan L; Linthorst GE; Desnick RJ;
    N Engl J Med; 2001 Jul; 345(1):9-16. PubMed ID: 11439963
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reduction of elevated plasma globotriaosylsphingosine in patients with classic Fabry disease following enzyme replacement therapy.
    van Breemen MJ; Rombach SM; Dekker N; Poorthuis BJ; Linthorst GE; Zwinderman AH; Breunig F; Wanner C; Aerts JM; Hollak CE
    Biochim Biophys Acta; 2011 Jan; 1812(1):70-6. PubMed ID: 20851180
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Impaired autophagic and mitochondrial functions are partially restored by ERT in Gaucher and Fabry diseases.
    Ivanova MM; Changsila E; Iaonou C; Goker-Alpan O
    PLoS One; 2019; 14(1):e0210617. PubMed ID: 30633777
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.