Evelise Brizola

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 4

Top Topics

Chemotherapy Induced

Top Venues

Molecular genetics & genomic medicine

Orphanet journal of rare diseases

Irish journal of medical science

International journal of molecular sciences

Istituto Ortopedico Rizzoli

Universidade Federal do Rio Grande do Sul (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Istituto Ortopedico Rizzoli

Italy

Researcher :: Department of Medical Genetics and Skeletal Rare Diseases

Education History

Universidade Federal do Rio Grande do Sul

Brazil

PHD

Publications

Maria Gnoli, Evelise Brizola, Morena Tremosini, Alessia Di Cecco, Luca Sangiorgi
Vitamin D and Bone fragility in Individuals with Osteogenesis Imperfecta: A Scoping Review. International journal of molecular sciences 24 (11) (2023)
Alberto Righi, Marina Pacheco, Stefania Cocchi, Sofia Asioli, Marco Gambarotti, Davide Maria Donati, Andrea Evangelista, Maria Gnoli, Manuela Locatelli, Marina Mordenti, Manila Boarini, Evelise Brizola, Elena Pedrini, Luca Sangiorgi
Secondary peripheral chondrosarcoma arising in solitary osteochondroma: variables influencing prognosis and survival. Orphanet journal of rare diseases 17 (1) (2022)
Luca Sangiorgi, Evelise Brizola, null null
The line between COVID-19 pandemic and rare bone diseases. Irish journal of medical science 190 (3) (2020)
Evelise Brizola, Maria Gnoli, Morena Tremosini, Paolo Nucci, Sara Bargiacchi, Andrea La Barbera, Sabrina Rita Giglio, Luca Sangiorgi
Variable clinical expression of Stickler Syndrome: A case report of a novel COL11A1 mutation. Molecular genetics & genomic medicine 8 (9) (2020)