Enzyme replacement therapy and beyond—in memoriam Roscoe O. Brady, M.D. (1923–2016)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-017-0032-8.pdf
Reference105 articles.
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2. Altarescu G, Hill S, Wiggs E et al (2001a) The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher’s disease. J Pediatr 138:539–547
3. Altarescu GM, Goldfarb LG, Park KY et al (2001b) Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease. Clin Genet 60:46–51
4. Anderson W (1898). A case of “angeiokeratoma”. Br J Dermatol 10:113–17
5. Barton NW, Furbish FS, Murray GJ, Garfield M, Brady RO (1990) Therapeutic response to intravenous infusions of glucocerebrosidase in a patient with Gaucher disease. Proc Natl Acad Sci U S A 87:1913–1916
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