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Items: 1 to 20 of 29

1.

Characterization of Fabry disease in 352 pediatric patients in the Fabry Registry.

Hopkin RJ, Bissler J, Banikazemi M, Clarke L, Eng CM, Germain DP, Lemay R, Tylki-Szymanska A, Wilcox WR.

Pediatr Res. 2008 Nov;64(5):550-5. doi: 10.1203/PDR.0b013e318183f132.

PMID:
18596579
2.

The heart in Anderson Fabry disease.

Kampmann C, Wiethoff CM, Perrot A, Beck M, Dietz R, Osterziel KJ.

Z Kardiol. 2002 Oct;91(10):786-95. Review.

PMID:
12395219
3.

[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
4.

[Neurological manifestations of Fabry disease].

Mendióroz M, Fernández-Cadenas I, Montaner J.

Rev Neurol. 2006 Dec 16-31;43(12):739-45. Review. Spanish.

5.

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
6.

Early therapeutic intervention in females with Fabry disease?

Hughes DA.

Acta Paediatr. 2008 Apr;97(457):41-7. doi: 10.1111/j.1651-2227.2008.00649.x. Review.

PMID:
18339187
7.

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
8.

Fabry disease: molecular genetics of the inherited nephropathy.

Desnick RJ, Astrin KH, Bishop DF.

Adv Nephrol Necker Hosp. 1989;18:113-27. Review.

PMID:
2564247
9.

Fabry disease: guidelines for the evaluation and management of multi-organ system involvement.

Eng CM, Germain DP, Banikazemi M, Warnock DG, Wanner C, Hopkin RJ, Bultas J, Lee P, Sims K, Brodie SE, Pastores GM, Strotmann JM, Wilcox WR.

Genet Med. 2006 Sep;8(9):539-48. Review.

PMID:
16980809
10.

Fabry disease: a review of current management strategies.

Mehta A, Beck M, Eyskens F, Feliciani C, Kantola I, Ramaswami U, Rolfs A, Rivera A, Waldek S, Germain DP.

QJM. 2010 Sep;103(9):641-59. doi: 10.1093/qjmed/hcq117. Epub 2010 Jul 21. Review.

11.

[Fabry disease. An interdisciplinary challenge].

Cybulla M, Neumann HP.

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

PMID:
17940933
12.

Renal complications of Fabry disease in children.

Najafian B, Mauer M, Hopkin RJ, Svarstad E.

Pediatr Nephrol. 2013 May;28(5):679-87. doi: 10.1007/s00467-012-2222-9. Epub 2012 Aug 17. Review.

13.

Cardiovascular manifestations of Fabry disease and the novel therapeutic strategies.

Seino Y, Takahashi H, Fukumoto H, Utsumi K, Hirai Y.

J Nippon Med Sch. 2005 Oct;72(5):254-61. Review.

14.

Fabry disease and the heart: an overview of the natural history and the effect of enzyme replacement therapy.

Shah JS, Elliott PM.

Acta Paediatr Suppl. 2005 Mar;94(447):11-4; discussion 9-10. Review.

PMID:
15895705
15.

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.

16.

Anderson-Fabry disease in children.

Sestito S, Ceravolo F, Concolino D.

Curr Pharm Des. 2013;19(33):6037-45. Review.

PMID:
23448455
17.

Fabry disease: cardiac manifestations and therapeutic options.

Pierre-Louis B, Kumar A, Frishman WH.

Cardiol Rev. 2009 Jan-Feb;17(1):31-5. doi: 10.1097/CRD.0b013e31818adc50. Review.

PMID:
19092368
18.

[Fabry disease in childhood].

Chabrol B, Mansour H, Cano A.

Presse Med. 2007 Mar;36 Spec No 1:1S32-5. Review. French.

PMID:
17546765
19.

[Cardiological follow-up in patients with Fabry disease].

Pieruzzi F, Pieroni M, Chimenti C, Frustaci A, Sarais C, Cecchi F; Area Cardiologica-Advisory Board Plan Multidisciplinare "Diagnosi e Follow-up Malattia di Fabry".

G Ital Cardiol (Rome). 2010 Jul-Aug;11(7-8):566-72. Review. Italian.

PMID:
21033333
20.

Effects of enzyme replacement therapy in Fabry disease--a comprehensive review of the medical literature.

Lidove O, West ML, Pintos-Morell G, Reisin R, Nicholls K, Figuera LE, Parini R, Carvalho LR, Kampmann C, Pastores GM, Mehta A.

Genet Med. 2010 Nov;12(11):668-79. doi: 10.1097/GIM.0b013e3181f13b75. Review.

PMID:
20962662
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