Long-term clinical outcomes in type 1 Gaucher disease following 10 years of imiglucerase treatment-Reference-Cited by-同舟云学术

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Long-term clinical outcomes in type 1 Gaucher disease following 10 years of imiglucerase treatment

Published:2012-09-14 Issue:3 Volume:36 Page:543-553
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Weinreb Neal J.,Goldblatt Jack,Villalobos Jacobo,Charrow Joel,Cole J. Alexander,Kerstenetzky Marcelo,vom Dahl Stephan,Hollak Carla

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10545-012-9528-4

Reference33 articles.

1. Andersson HC, Charrow J, Kaplan P, Mistry P, Pastores GM, Prakash-Cheng A et al (2005) Individualization of long-term enzyme replacement therapy for Gaucher disease. Genet Med 7:105–110

2. Barton NW, Brady RO, Dambrosia JM, Di Bisceglie AM, Doppelt SH, Hill SC et al (1991) Replacement therapy for inherited enzyme deficiency—macrophage-targeted glucocerebrosidase for Gaucher’s disease. N Engl J Med 324:1464–1470

3. Biegstraaten M, van Schaik IN, Aerts JM, Hollak CE (2008) ‘Non-neuronopathic’ Gaucher disease reconsidered. Prevalence of neurological manifestations in a Dutch cohort of type I Gaucher disease patients and a systematic review of the literature. J Inherit Metab Dis 31:337–349

4. Charrow J, Andersson HC, Kaplan P, Kolodny EH, Mistry P, Pastores G et al (2000) The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease. Arch Intern Med 160:2835–2843

5. Charrow J, Dulisse B, Grabowski GA, Weinreb NJ (2007) The effect of enzyme replacement therapy on bone crisis and bone pain in patients with type 1 Gaucher disease. Clin Genet 71:205–211

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