Long-term efficacy and safety results of taliglucerase alfa through 5 years in adult treatment-naïve patients with Gaucher disease

Author:

Zimran Ari,Durán Gloria,Giraldo Pilar,Rosenbaum Hanna,Giona Fiorina,Petakov Milan,Terreros Muñoz Eduardo,Solorio-Meza Sergio Eduardo,Cooper Peter A.,Varughese Sheeba,Alon Sari,Chertkoff Raul

Funder

Protalix BioTherapeutics

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference15 articles.

1. Gaucher disease and related lysosomal storage diseases;Zimran,2016

2. Gaucher disease: phenotypic and genetic variation;Grabowski,2010

3. The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease;Charrow;Arch. Intern. Med.,2000

4. Understanding the natural history of Gaucher disease;Mistry;Am. J. Hematol.,2015

5. Replacement therapy for inherited enzyme deficiency–macrophage-targeted glucocerebrosidase for Gaucher's disease;Barton;N. Engl. J. Med.,1991

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