What’s in the Literature?
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Neurology,General Medicine
Reference19 articles.
1. 1. Eng CM, Guffon N, Wilcox WR, et al. Safety and efficacy of recombinant human -galactosidase A replacement therapy in Fabrys disease.;N Engl J Med,2001
2. 2. Schiffman R, Kopp JB, Austin HA, et al. Enzyme replacement therapy in Fabry disease. A randomized controlled trial.;JAMA,2001
3. 3. Hilz MJ, Brys M, Marthol H, et al. Enzyme replacement therapy improves function of C-, A-, and A-nerve fibers in Fabry neuropathy.;Neurology,2004
4. 4. Winkel LPF, Kamphoven JHJ, Van den Hout HJMP, et al. Morphological changes in muscle tissue of patients with infantile Pompes disease receiving enzyme replacement therapy.;Muscle Nerve,2003
5. 5. Winkel LPF, Van den Hout JMP, Kamphoven JHJ, et al. Enzyme replacement therapy in late-onset Pompes disease: a three-year follow-up.;Ann Neurol,2004
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