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Orphanet Journal of Rare Diseases|March 21, 2014
A population-based registry as a source of health indicators for rare diseases: the ten-year experience of the Veneto Region's rare diseases registryMonica Mazzucato, Laura Visonà Dalla Pozza, Silvia Manea, et al.Orphanet Journal of Rare Diseases|November 18, 2023
Estimating mortality in rare diseases using a population-based registry, 2002 through 2019Monica Mazzucato, Laura Visonà Dalla Pozza, Cinzia Minichiello, et al.Frontiers in Pharmacology|October 17, 2022
Real-world use of orphan medicinal products (OMPs) in rare disease (RD) patients: A population-based registry studyMonica Mazzucato, Cinzia Minichiello, Andrea Vianello, et al.International Journal of Environmental Research and Public Health|October 13, 2018
The Epidemiology of Transition into Adulthood of Rare Diseases Patients: Results from a Population-Based RegistryMonica Mazzucato, Laura Visonà Dalla Pozza, Cinzia Minichiello, et al.Recenti Progressi in Medicina|July 19, 2022
[The impact of the use of treatments not included in the reimbursement classes in the care of rare patients: a real world study.]Monica Mazzucato, Cinzia Minichiello, Laura Visonà Dalla Pozza, et al.Health Services Management Research|January 10, 2023
High-cost drugs for rare diseases: their expenditure and value based on a regional area-based studySilvia Manea, Laura Visonà Dalla Pozza, Cinzia Minichiello, et al.European Geriatric Medicine|February 23, 2026
Aging and rare diseases: from epidemiology to a call to actionMonica Mazzucato, Giulia Fanton, Andrea Vianello, et al.Pageof 1