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Last Updated: 10/31/2025
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Found 59 publications
Ten-Year Follow-Up of Taliglucerase Alfa in Type 1 Gaucher Disease: Real-World Evidence from Albania.
Journal: Journal of clinical medicine
Published: September 02, 2025
Real-world experience of switching to taliglucerase among patients with Gaucher disease in Québec: A case series.
Journal: Molecular genetics and metabolism reports
Published: January 03, 2025
Plant molecular farming: a promising frontier for orphan drug production.
Journal: Biotechnology letters
Published: August 01, 2024
Taliglucerase alfa in the longterm treatment of children and adolescents with type 1 Gaucher disease: the Albanian experience.
Journal: Frontiers in pediatrics
Published: December 07, 2023
Real-World Experiences with Taliglucerase Alfa Home Infusions for Patients with Gaucher Disease: A Global Cohort Study.
Journal: Journal of clinical medicine
Published: August 02, 2023
The Bone Biomarker of Quantitative Chemical Shift Imaging in Patients with Type 1 Gaucher Disease Receiving Low-Dose Long-Term Enzyme Replacement Therapy.
Journal: Journal of clinical medicine
Published: January 05, 2023
A Systematic Review and Meta-analyses of Longitudinal Studies on Drug Treatments for Gaucher Disease.
Journal: The Annals of pharmacotherapy
Published: July 11, 2022
The budget impact of enzyme replacement therapy in type 1 Gaucher disease in the United States.
Journal: Journal of medical economics
Published: May 25, 2022
Safety and effectiveness of taliglucerase alfa in patients with Gaucher disease: an interim analysis of real-world data from a multinational drug registry (TALIAS).
Journal: Orphanet journal of rare diseases
Published: December 20, 2021
Impact of Long-Term Enzyme Replacement Therapy on Glucosylsphingosine (Lyso-Gb1) Values in Patients with Type 1 Gaucher Disease: Statistical Models for Comparing Three Enzymatic Formulations.
Journal: International journal of molecular sciences
Published: May 22, 2021
Last Updated: 10/31/2025