BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

369 related articles for article (PubMed ID: 34748189)

  • 21. Agalsidase alfa: a review of its use in the management of Fabry disease.
    Keating GM
    BioDrugs; 2012 Oct; 26(5):335-54. PubMed ID: 22946754
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Assessment and impact of dose escalation on anti-drug antibodies in Fabry disease.
    Lenders M; Brand E
    Front Immunol; 2022; 13():1024963. PubMed ID: 36569886
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Agalsidase-β should be proposed as first line therapy in classic male Fabry patients with undetectable α-galactosidase A activity.
    Nowak A; Dormond O; Monzambani V; Huynh-Do U; Barbey F
    Mol Genet Metab; 2022; 137(1-2):173-178. PubMed ID: 36087505
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Risk factors for severe clinical events in male and female patients with Fabry disease treated with agalsidase beta enzyme replacement therapy: Data from the Fabry Registry.
    Hopkin RJ; Cabrera G; Charrow J; Lemay R; Martins AM; Mauer M; Ortiz A; Patel MR; Sims K; Waldek S; Warnock DG; Wilcox WR
    Mol Genet Metab; 2016 Sep; 119(1-2):151-9. PubMed ID: 27510433
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Anti-BlyS antibody reduces the immune reaction against enzyme and enhances the efficacy of enzyme replacement therapy in Fabry disease model mice.
    Sato Y; Ida H; Ohashi T
    Clin Immunol; 2017 May; 178():56-63. PubMed ID: 28161408
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Agalsidase Beta: a review of its use in the management of Fabry disease.
    Keating GM; Simpson D
    Drugs; 2007; 67(3):435-55. PubMed ID: 17335299
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The use of agalsidase alfa enzyme replacement therapy in the treatment of Fabry disease.
    Morel CF; Clarke JT
    Expert Opin Biol Ther; 2009 May; 9(5):631-9. PubMed ID: 19368525
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Enzyme replacement therapy in heterozygous females with Fabry disease: results of a phase IIIB study.
    Baehner F; Kampmann C; Whybra C; Miebach E; Wiethoff CM; Beck M
    J Inherit Metab Dis; 2003; 26(7):617-27. PubMed ID: 14707510
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Long-term safety and efficacy of pegunigalsidase alfa: A multicenter 6-year study in adult patients with Fabry disease.
    Hughes D; Gonzalez D; Maegawa G; Bernat JA; Holida M; Giraldo P; Atta MG; Chertkoff R; Alon S; Almon EB; Rocco R; Goker-Alpan O
    Genet Med; 2023 Dec; 25(12):100968. PubMed ID: 37634127
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A Fabry Disease Patient Who Developed Hypersensitivity Reaction against Agalsidase Beta following COVID-19 Infection.
    Sonmez O; Ozcan SG; Trabulus S; Seyahi N
    Nephron; 2023; 147(3-4):199-202. PubMed ID: 36174537
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Head-to-head trial of pegunigalsidase alfa versus agalsidase beta in patients with Fabry disease and deteriorating renal function: results from the 2-year randomised phase III BALANCE study.
    Wallace EL; Goker-Alpan O; Wilcox WR; Holida M; Bernat J; Longo N; Linhart A; Hughes DA; Hopkin RJ; Tøndel C; Langeveld M; Giraldo P; Pisani A; Germain DP; Mehta A; Deegan PB; Molnar MJ; Ortiz D; Jovanovic A; Muriello M; Barshop BA; Kimonis V; Vujkovac B; Nowak A; Geberhiwot T; Kantola I; Knoll J; Waldek S; Nedd K; Karaa A; Brill-Almon E; Alon S; Chertkoff R; Rocco R; Sakov A; Warnock DG
    J Med Genet; 2024 May; 61(6):520-530. PubMed ID: 37940383
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Fabry Disease Therapy: State-of-the-Art and Current Challenges.
    Azevedo O; Gago MF; Miltenberger-Miltenyi G; Sousa N; Cunha D
    Int J Mol Sci; 2020 Dec; 22(1):. PubMed ID: 33379210
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Switch from enzyme replacement therapy to oral chaperone migalastat for treating fabry disease: real-life data.
    Riccio E; Zanfardino M; Ferreri L; Santoro C; Cocozza S; Capuano I; Imbriaco M; Feriozzi S; Pisani A;
    Eur J Hum Genet; 2020 Dec; 28(12):1662-1668. PubMed ID: 32647377
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Spotlight on agalsidase beta in Fabry disease.
    Keating GM; Simpson D
    BioDrugs; 2007; 21(4):269-71. PubMed ID: 17628124
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [The treatment for Fabry disease: focus on agalsidase alpha and beta].
    Nisticò R; Pisani A
    Recenti Prog Med; 2021 Oct; 112(10):75e-84e. PubMed ID: 34647542
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Pathogenesis and Molecular Mechanisms of Anderson-Fabry Disease and Possible New Molecular Addressed Therapeutic Strategies.
    Tuttolomondo A; Simonetta I; Riolo R; Todaro F; Di Chiara T; Miceli S; Pinto A
    Int J Mol Sci; 2021 Sep; 22(18):. PubMed ID: 34576250
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Significant improvement in Fabry disease podocytopathy after 3 years of treatment with agalsidase beta.
    Ito S; Ogura M; Kamei K; Matsuoka K; Warnock DG
    Pediatr Nephrol; 2016 Aug; 31(8):1369-73. PubMed ID: 27129690
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The effect of enzyme replacement therapy on clinical outcomes in paediatric patients with Fabry disease - A systematic literature review by a European panel of experts.
    Spada M; Baron R; Elliott PM; Falissard B; Hilz MJ; Monserrat L; Tøndel C; Tylki-Szymańska A; Wanner C; Germain DP
    Mol Genet Metab; 2019 Mar; 126(3):212-223. PubMed ID: 29785937
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.