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Items: 1 to 20 of 124

1.

Renal transplantation between siblings with unrecognized Fabry disease.

Taneda S, Honda K, Nakajima I, Huchinoue S, Oda H.

Transplant Proc. 2013 Jan-Feb;45(1):115-8. doi: 10.1016/j.transproceed.2012.10.024.

PMID:
23375284
2.

Unexpected Fabry disease in a renal allograft kidney: an underrecognized cause of poor allograft function.

Kochar O, Wick MR, Kerr SE, Oglesbee D, Cathro HP.

Ultrastruct Pathol. 2011 Apr;35(2):92-6. doi: 10.3109/01913123.2010.538136.

PMID:
21299350
3.

Kidney transplantation from a mother with unrecognized Fabry disease to her son with low α-galactosidase A activity: A 14-year follow-up without enzyme replacement therapy.

Odani K, Okumi M, Honda K, Ishida H, Tanabe K.

Nephrology (Carlton). 2016 Jul;21 Suppl 1:57-9. doi: 10.1111/nep.12771.

PMID:
26971403
4.

Anderson-Fabry disease in kidneys from deceased donor.

Basic-Jukic N, Coric M, Kes P, Bubic-Filipi LJ, Pasini J, Mokos I.

Am J Transplant. 2007 Dec;7(12):2829-33. Epub 2007 Oct 17.

5.

Kidney transplantation and enzyme alpha-galactosidase A therapy in patient with Fabry disease: a case report.

Dziemianko I, Jezior D, Boratyńska M, Patrzałek D, Kuźniar J, Szyber P, Klinger M.

Transplant Proc. 2007 Nov;39(9):2925-7.

PMID:
18022018
6.

Long-term enzyme replacement therapy is associated with reduced proteinuria and preserved proximal tubular function in women with Fabry disease.

Prabakaran T, Birn H, Bibby BM, Regeniter A, Sørensen SS, Feldt-Rasmussen U, Nielsen R, Christensen EI.

Nephrol Dial Transplant. 2014 Mar;29(3):619-25. doi: 10.1093/ndt/gft452. Epub 2013 Nov 8.

PMID:
24215016
7.

[Anderson-Fabry disease and renal transplantation].

Basić-Jukić N, Kes P, Hudolin T, Mesar I, Corić M, Kastelan Z.

Acta Med Croatica. 2011;65(4):377-80. Croatian.

PMID:
22359912
8.

Combined heart and kidney transplantation in a patient with Fabry disease in the enzyme replacement therapy era.

Karras A, De Lentdecker P, Delahousse M, Debauchez M, Tricot L, Pastural M, Bruneval P, Zemoura L, Duong Van Huyen JP, Lidove O.

Am J Transplant. 2008 Jun;8(6):1345-8. doi: 10.1111/j.1600-6143.2008.02245.x.

9.
10.

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. doi: 10.1007/s10545-008-0930-x. Epub 2008 Oct 21.

PMID:
18937048
11.

Dialysis and transplantation in Fabry disease: indications for enzyme replacement therapy.

Mignani R, Feriozzi S, Schaefer RM, Breunig F, Oliveira JP, Ruggenenti P, Sunder-Plassmann G.

Clin J Am Soc Nephrol. 2010 Feb;5(2):379-85. doi: 10.2215/CJN.05570809. Epub 2010 Jan 7. Review.

12.

Novel frameshift mutation in a heterozygous woman with Fabry disease and end-stage renal failure.

Van Loo A, Vanholder R, Madsen K, Praet M, Kint J, De Paepe A, Messiaen L, Lameire N, Hasholt L, Sørensen SA, Ringoir S.

Am J Nephrol. 1996;16(4):352-7.

PMID:
8739292
13.

Chronic renal failure and proteinuria in adulthood: Fabry disease predominantly affecting the kidneys.

Cybulla M, Schaefer E, Wendt S, Ling H, Kröber SM, Hövelborn U, Schandelmaier S, Rohrbach R, Neumann HP.

Am J Kidney Dis. 2005 May;45(5):e82-9.

PMID:
15861341
14.

Fabry disease: detection of undiagnosed hemodialysis patients and identification of a "renal variant" phenotype.

Nakao S, Kodama C, Takenaka T, Tanaka A, Yasumoto Y, Yoshida A, Kanzaki T, Enriquez AL, Eng CM, Tanaka H, Tei C, Desnick RJ.

Kidney Int. 2003 Sep;64(3):801-7.

15.

Fabry disease. A case report.

Kotnik J, Kotnik F, Desnick RJ.

Acta Dermatovenerol Alp Pannonica Adriat. 2005 Mar;14(1):15-9.

16.

Update on Fabry disease: kidney involvement, renal progression and enzyme replacement therapy.

Breunig F, Wanner C.

J Nephrol. 2008 Jan-Feb;21(1):32-7. Review.

PMID:
18264934
17.

Enzyme replacement therapy for Fabry disease, an inherited nephropathy.

Desnick RJ, Banikazemi M, Wasserstein M.

Clin Nephrol. 2002 Jan;57(1):1-8. Review.

PMID:
11837797
18.

End-stage renal disease in patients with Fabry disease: natural history data from the Fabry Registry.

Ortiz A, Cianciaruso B, Cizmarik M, Germain DP, Mignani R, Oliveira JP, Villalobos J, Vujkovac B, Waldek S, Wanner C, Warnock DG.

Nephrol Dial Transplant. 2010 Mar;25(3):769-75. doi: 10.1093/ndt/gfp554. Epub 2009 Oct 21.

PMID:
19846394
19.

Kidney transplantation and enzyme replacement therapy in patients with Fabry disease.

Cybulla M, Kurschat C, West M, Nicholls K, Torras J, Sunder-Plassmann G, Feriozzi S.

J Nephrol. 2013 Jul-Aug;26(4):645-51. doi: 10.5301/jn.5000214. Epub 2012 Sep 19. Review.

PMID:
23023720
20.

The kidney in Fabry's disease.

Pisani A, Visciano B, Imbriaco M, Di Nuzzi A, Mancini A, Marchetiello C, Riccio E.

Clin Genet. 2014 Oct;86(4):301-9. doi: 10.1111/cge.12386. Epub 2014 May 30.

PMID:
24645664

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