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Items: 1 to 20 of 44

1.

Enzyme replacement therapy improves function of C-, Adelta-, and Abeta-nerve fibers in Fabry neuropathy.

Hilz MJ, Brys M, Marthol H, Stemper B, Dütsch M.

Neurology. 2004 Apr 13;62(7):1066-72.

PMID:
15079003
2.

Neuropathy and Fabry disease: pathogenesis and enzyme replacement therapy.

Schiffmann R.

Acta Neurol Belg. 2006 Jun;106(2):61-5. Review.

PMID:
16898255
3.

Enzyme replacement therapy for Fabry disease: a systematic review of available evidence.

Schaefer RM, Tylki-Szymańska A, Hilz MJ.

Drugs. 2009 Nov 12;69(16):2179-205. doi: 10.2165/11318300-000000000-00000. Review.

PMID:
19852524
4.

A systematic review of the clinical effectiveness and cost-effectiveness of enzyme replacement therapies for Fabry's disease and mucopolysaccharidosis type 1.

Connock M, Juarez-Garcia A, Frew E, Mans A, Dretzke J, Fry-Smith A, Moore D.

Health Technol Assess. 2006 Jun;10(20):iii-iv, ix-113. Review.

5.

Fabry disease.

Toyooka K.

Handb Clin Neurol. 2013;115:629-42. doi: 10.1016/B978-0-444-52902-2.00037-0. Review.

PMID:
23931807
6.

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. doi: 10.1517/14712590902902296 . Review.

PMID:
19368525
7.

Enzyme replacement therapy in Fabry's disease: recent advances and clinical applications.

Mignani R, Cagnoli L.

J Nephrol. 2004 May-Jun;17(3):354-63. Review.

PMID:
15365954
8.

Clinical results of enzyme replacement therapy in Fabry disease: a comprehensive review of literature.

Lidove O, Joly D, Barbey F, Bekri S, Alexandra JF, Peigne V, Jaussaud R, Papo T.

Int J Clin Pract. 2007 Feb;61(2):293-302. Review.

PMID:
17263716
9.

[Clinical efficacy of enzyme replacement therapy in Fabry disease. A critical review].

Lidove O, Papo T.

Rev Med Interne. 2009 Oct;30(10):920-9. doi: 10.1016/j.revmed.2009.04.003. Epub 2009 Jun 12. Review. French.

PMID:
19524334
10.

Enzyme replacement therapy in Fabry disease.

Brady RO, Murray GJ, Moore DF, Schiffmann R.

J Inherit Metab Dis. 2001;24 Suppl 2:18-24; discussion 11-2. Review.

PMID:
11758675
11.

Enzyme replacement therapy of Fabry disease.

Clarke JT, Iwanochko RM.

Mol Neurobiol. 2005 Aug;32(1):43-50. Review.

PMID:
16077182
12.

Spotlight on agalsidase beta in Fabry disease.

Keating GM, Simpson D.

BioDrugs. 2007;21(4):269-71. Review.

PMID:
17628124
13.

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.

14.

[Development of an orphan drug to treat a genetic disease: the paradigm of agalsidase beta].

Germain DP, Benistan K.

Presse Med. 2007 Mar;36 Spec No 1:1S69-75. Review. French.

PMID:
17546772
15.

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

Keating GM, Simpson D.

Drugs. 2007;67(3):435-55. Review.

PMID:
17335299
16.

[Fabry disease : diagnosis and treatment].

Üçeyler N, Sommer C.

Schmerz. 2012 Sep;26(5):609-19. doi: 10.1007/s00482-012-1238-1. Review. German.

PMID:
23052995
17.

Fabry disease.

Toyooka K.

Curr Opin Neurol. 2011 Oct;24(5):463-8. doi: 10.1097/WCO.0b013e32834a9433. Review.

PMID:
21825987
18.

Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy.

Desnick RJ, Brady R, Barranger J, Collins AJ, Germain DP, Goldman M, Grabowski G, Packman S, Wilcox WR.

Ann Intern Med. 2003 Feb 18;138(4):338-46. Review.

PMID:
12585833
19.

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
20.

Neurological features of Fabry disease: clinical, pathophysiological aspects and therapy.

Bersano A, Lanfranconi S, Valcarenghi C, Bresolin N, Micieli G, Baron P.

Acta Neurol Scand. 2012 Aug;126(2):77-97. doi: 10.1111/j.1600-0404.2012.01661.x. Epub 2012 Mar 19. Review.

PMID:
22428782
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