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Frontiers in Medicine|October 22, 2021
Opportunities and Challenges for Machine Learning in Rare DiseasesSergio Decherchi, Elena Pedrini, Marina Mordenti, et al.
Frontiers in Pharmacology|October 10, 2022
Remodeling an existing rare disease registry to be used in regulatory context: Lessons learned and recommendationsMarina Mordenti, Manila Boarini, Fabio D'Alessandro, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Validation of a new multiple osteochondromas classification through Switching Neural NetworksMarina Mordenti, Enrico Ferrari, Elena Pedrini, et al.
Frontiers in Endocrinology|June 3, 2026
Osteogenesis imperfecta: a registry-based study of the clinical symptoms of disease in a large cohort of Italian patientsMarina Mordenti, James Clancy, Matthew Dyer, et al.
Journal of Clinical Laboratory Analysis|June 6, 2022
Preanalytical DNA assessment for downstream applications: How to optimize the management of human biospecimens to support molecular diagnosis-An experimental studyMarina Mordenti, Valentina Capicchioni, Serena Corsini, et al.
BMC Health Services Research|November 21, 2023
Cost-effectiveness of bringing a nurse into an Italian genetic day clinic: a before and after studyMarina Mordenti, Morena Tremosini, Manuela Locatelli, et al.
Bone|June 28, 2020
The natural history of multiple osteochondromas in a large Italian cohort of pediatric patientsMarina Mordenti, Fei Shih, Manila Boarini, et al.
Journal of Bone Oncology|April 10, 2025
Pain in patients with multiple inherited osteochondromas: Incidence and potential prognostic factors. A retrospective cohort studyMorena Tremosini, Mattia Morri, Cristiana Forni, et al.
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