Similar articles for PMID: 15086478

Year	Number of Results
1979	1
2000	3
2001	5
2002	3
2003	14
2004	22
2005	22
2006	29
2007	38
2008	22
2009	31
2010	25
2011	19
2012	21
2013	19
2014	14
2015	21
2016	16
2017	21
2018	19
2019	18
2020	16
2021	20
2022	19
2023	5
2024	0

1

Enzyme replacement therapy with agalsidase beta in kidney transplant patients with Fabry disease: a pilot study.

Mignani R, Panichi V, Giudicissi A, Taccola D, Boscaro F, Feletti C, Moneti G, Cagnoli L. Mignani R, et al. Kidney Int. 2004 Apr;65(4):1381-5. doi: 10.1111/j.1523-1755.2004.00514.x. Kidney Int. 2004. PMID: 15086478 Free article.

2

Agalsidase therapy in patients with Fabry disease on renal replacement therapy: a nationwide study in Italy.

Mignani R, Feriozzi S, Pisani A, Cioni A, Comotti C, Cossu M, Foschi A, Giudicissi A, Gotti E, Lozupone VA, Marchini F, Martinelli F, Bianco F, Panichi V, Procaccini DA, Ragazzoni E, Serra A, Soliani F, Spinelli L, Torti G, Veroux M, Cianciaruso B, Cagnoli L. Mignani R, et al. Nephrol Dial Transplant. 2008 May;23(5):1628-35. doi: 10.1093/ndt/gfm813. Epub 2007 Dec 5. Nephrol Dial Transplant. 2008. PMID: 18057066

3

Agalsidase alfa: a review of its use in the management of Fabry disease.

Keating GM. Keating GM. BioDrugs. 2012 Oct 1;26(5):335-54. doi: 10.2165/11209690-000000000-00000. BioDrugs. 2012. PMID: 22946754 Review.

4

Efficacy and safety of enzyme-replacement-therapy with agalsidase alfa in 36 treatment-naïve Fabry disease patients.

Tsuboi K, Yamamoto H. Tsuboi K, et al. BMC Pharmacol Toxicol. 2017 Jun 7;18(1):43. doi: 10.1186/s40360-017-0152-7. BMC Pharmacol Toxicol. 2017. PMID: 28592315 Free PMC article.

5

Safety and effectiveness of enzyme replacement therapy with agalsidase alfa in patients with Fabry disease: Post-marketing surveillance in Japan.

Sasa H, Nagao M, Kino K. Sasa H, et al. Mol Genet Metab. 2019 Apr;126(4):448-459. doi: 10.1016/j.ymgme.2019.02.005. Epub 2019 Feb 20. Mol Genet Metab. 2019. PMID: 30803893 Free article.

6

Kidney function and 24-hour proteinuria in patients with Fabry disease during 36 months of agalsidase alfa enzyme replacement therapy: a Brazilian experience.

Thofehrn S, Netto C, Cecchin C, Burin M, Matte U, Brustolin S, Nunes AC, Coelho J, Tsao M, Jardim L, Giugliani R, Barros EJ. Thofehrn S, et al. Ren Fail. 2009;31(9):773-8. doi: 10.3109/08860220903150296. Ren Fail. 2009. PMID: 19925283 Clinical Trial.

7

Kidney transplantation in patients with Fabry disease.

Cybulla M, Walter KN, Schwarting A, Divito R, Feriozzi S, Sunder-Plassmann G; European FOS Investigators Group. Cybulla M, et al. Transpl Int. 2009 Apr;22(4):475-81. doi: 10.1111/j.1432-2277.2008.00824.x. Epub 2009 Jan 22. Transpl Int. 2009. PMID: 19207191 Free article.

8

A retrospective analysis of the potential impact of IgG antibodies to agalsidase beta on efficacy during enzyme replacement therapy for Fabry disease.

Bénichou B, Goyal S, Sung C, Norfleet AM, O'Brien F. Bénichou B, et al. Mol Genet Metab. 2009 Jan;96(1):4-12. doi: 10.1016/j.ymgme.2008.10.004. Epub 2008 Nov 20. Mol Genet Metab. 2009. PMID: 19022694 Clinical Trial.

9

[Fabry disease in Spain: first analysis of the response to enzyme replacement therapy].

Rivera Gallego A, López Rodríguez M, Barbado Hernández FJ, Barba Romero MA, García de Lorenzo Y Mateos A, Pintos Morelle G; Grupo Español de Estudio de Fabry Outcome Survey. Rivera Gallego A, et al. Med Clin (Barc). 2006 Oct 7;127(13):481-4. doi: 10.1157/13093265. Med Clin (Barc). 2006. PMID: 17043001 Spanish.

10

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. Baehner F, et al. J Inherit Metab Dis. 2003;26(7):617-27. doi: 10.1023/b:boli.0000005658.14563.77. J Inherit Metab Dis. 2003. PMID: 14707510 Clinical Trial.

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