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Items: 1 to 20 of 83

1.

Fabry disease: a review of ophthalmic and systemic manifestations.

Sivley MD.

Optom Vis Sci. 2013 Feb;90(2):e63-78. doi: 10.1097/OPX.0b013e31827ec7eb. Review.

PMID:
23334311
2.

The heart in Fabry's disease.

Sheppard MN.

Cardiovasc Pathol. 2011 Jan-Feb;20(1):8-14. doi: 10.1016/j.carpath.2009.10.003. Epub 2009 Nov 17. Review.

PMID:
19919901
3.

Fabry disease.

Tarabuso AL.

Skinmed. 2011 May-Jun;9(3):173-7. Review.

PMID:
21675497
4.

Fabry disease in children: correlation between ocular manifestations, genotype and systemic clinical severity.

Allen LE, Cosgrave EM, Kersey JP, Ramaswami U.

Br J Ophthalmol. 2010 Dec;94(12):1602-5. doi: 10.1136/bjo.2009.176651. Epub 2010 Jun 24.

PMID:
20576773
5.

Ocular features of Fabry disease: diagnosis of a treatable life-threatening disorder.

Samiy N.

Surv Ophthalmol. 2008 Jul-Aug;53(4):416-23. doi: 10.1016/j.survophthal.2008.04.005. Review.

PMID:
18572058
6.

Fabry disease: treatment and diagnosis.

Rozenfeld PA.

IUBMB Life. 2009 Nov;61(11):1043-50. doi: 10.1002/iub.257.

7.

Long-term correction of globotriaosylceramide storage in Fabry mice by recombinant adeno-associated virus-mediated gene transfer.

Park J, Murray GJ, Limaye A, Quirk JM, Gelderman MP, Brady RO, Qasba P.

Proc Natl Acad Sci U S A. 2003 Mar 18;100(6):3450-4. Epub 2003 Mar 6.

8.

[Ophthalmic manifestations in Mexican patients with Fabry disease].

Beltrán-Becerra KJ, Ríos-González BE, Gutiérrez-Amavizca BE, Silva-Noriega DA, Figuera LE.

Arch Soc Esp Oftalmol. 2012 Nov;87(11):373-5. doi: 10.1016/j.oftal.2011.09.008. Epub 2012 May 24. Spanish.

PMID:
23058197
9.

[Fabry disease. An interdisciplinary challenge].

Cybulla M, Neumann HP.

Dtsch Med Wochenschr. 2007 Oct;132(43):2271-7. Review. German.

PMID:
17940933
10.

Ocular manifestations of Fabry disease within in a single kindred.

Morier AM, Minteer J, Tyszko R, McCann R, Clarke MV, Browning MF.

Optometry. 2010 Sep;81(9):437-49. doi: 10.1016/j.optm.2010.02.011. Epub 2010 Jul 8.

PMID:
20615758
11.

[Pathophysiological aspects of brain structural disturbances in patients with Fabry disease: literature review].

Nill M, Müller MJ, Beck M, Stoeter P, Fellgiebel A.

Fortschr Neurol Psychiatr. 2006 Dec;74(12):687-95. Review. German.

PMID:
17167727
12.

Anderson-Fabry disease: developments in diagnosis and treatment.

Kes VB, Cesarik M, Zavoreo I, Madzar Z, Demarin V.

Acta Clin Croat. 2012 Sep;51(3):411-7. Review.

PMID:
23330407
13.

Renal manifestations in Fabry disease and therapeutic options.

Torra R.

Kidney Int Suppl. 2008 Dec;(111):S29-32. doi: 10.1038/ki.2008.522. Review.

PMID:
19039306
14.
15.

Fabry disease: clinical spectrum and evidence-based enzyme replacement therapy.

Desnick RJ, Banikazemi M.

Nephrol Ther. 2006 Jan;2 Suppl 2:S172-85.

PMID:
17373219
16.

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. Epub 2007 May 4.

PMID:
17483124
17.

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
18.

Interdisciplinary approach towards female patients with Fabry disease.

Weidemann F, Niemann M, Sommer C, Beer M, Breunig F, Wanner C.

Eur J Clin Invest. 2012 Apr;42(4):455-62. doi: 10.1111/j.1365-2362.2011.02614.x. Epub 2011 Nov 3. Review.

PMID:
22049975
19.

Identification of a novel mutation and prevalence study for fabry disease in Japanese dialysis patients.

Nishino T, Obata Y, Furusu A, Hirose M, Shinzato K, Hattori K, Nakamura K, Matsumoto T, Endo F, Kohno S.

Ren Fail. 2012;34(5):566-70. doi: 10.3109/0886022X.2012.669300.

PMID:
22563919
20.

Narrative review: Fabry disease.

Clarke JT.

Ann Intern Med. 2007 Mar 20;146(6):425-33. Review.

PMID:
17371887

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