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Expert Review of Endocrinology & Metabolism|February 16, 2019
Agalsidase alfa for enzyme-replacement therapy in Fabry diseaseAtul MehtaHospital Medicine (London, England : 1998)|July 5, 2002
Agalsidase alfa: specific treatment for Fabry diseaseAtul MehtaEuropean Journal of Internal Medicine|October 3, 2006
Epidemiology and natural history of Gaucher's diseaseAtul MehtaEuropean Journal of Internal Medicine|October 3, 2006
Clinical experience with substrate reduction therapyAtul MehtaMedicina Clinica|January 11, 2012
Gaucher's disease: the changing paradigm of a lysosomal disorderAtul MehtaJournal of Clinical Medicine|September 27, 2025
Interstitial Lung Disease in 2025-Progress, Challenges, and Hope AheadSameep Sehgal, Atul MehtaThe Clinical Biochemist. Reviews|June 11, 2020
Laboratory Diagnosis of Lysosomal Diseases: Newborn Screening to TreatmentMaria FullerLipids in Health and Disease|October 13, 2010
Sphingolipids: the nexus between Gaucher disease and insulin resistanceMaria FullerBritish Journal of Nursing (Mark Allen Publishing)|March 26, 2008
Home therapy for lysosomal storage disordersDerryalynn A Hughes, Alan Mlilligan, Atul MehtaPageof 24