Maria Gnoli

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Topics

Peritoneal Dialysis

Chronic Kidney Disease

Clinical Practice

Prognostic Factors

Top Venues

Orphanet journal of rare diseases

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

European journal of human genetics : EJHG

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

Publications

Maria Gnoli, Marco Gambarotti, Alberto Righi, Eric Lodewijk Staals, Andrea Evangelista, Morena Tremosini, Evelise Brizola, Marina Mordenti, Manila Boarini, Manuela Locatelli, Elena Pedrini, Luca Sangiorgi
Secondary peripheral chondrosarcoma in multiple osteochondromas: a retrospective single-institution case series. Orphanet journal of rare diseases 19 (1) (2024)
Maria Gnoli, Marco Gambarotti, Alberto Righi, Eric Lodewijk Staals, Andrea Evangelista, Morena Tremosini, Evelise Brizola, Marina Mordenti, Manila Boarini, Manuela Locatelli, Elena Pedrini, Luca Sangiorgi
Secondary peripheral chondrosarcoma in multiple osteochondromas: a retrospective single-institution case series. Orphanet journal of rare diseases 19 (1) (2024)
Maria Gnoli, Marco Gambarotti, Alberto Righi, Eric Lodewijk Staals, Andrea Evangelista, Morena Tremosini, Evelise Brizola, Marina Mordenti, Manila Boarini, Manuela Locatelli, Elena Pedrini, Luca Sangiorgi
Secondary peripheral chondrosarcoma in multiple osteochondromas: a retrospective single-institution case series. Orphanet journal of rare diseases 19 (1) (2024)
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)
Marina Mordenti, Maria Gnoli, Manila Boarini, Giovanni Trisolino, Andrea Evangelista, Elena Pedrini, Serena Corsini, Morena Tremosini, Eric L Staals, Diego Antonioli, Stefano Stilli, Davide M Donati, Luca Sangiorgi
The Rizzoli Multiple Osteochondromas Classification revised: describing the phenotype to improve clinical practice. American journal of medical genetics. Part A 185 (11) (2021)
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)
Maria Gnoli, Eric Lodewijk Staals, Laura Campanacci, Maria Francesca Bedeschi, Flavio Faletra, Salvatore Gallone, Agostino Gaudio, Teresa Mattina, Fiorella Gurrieri, Antonio Percesepe, Iria Neri, Annalucia Virdi, Morena Tremosini, Annamaria Milanesi, Evelise Brizola, Elena Pedrini, Luca Sangiorgi
Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case Series. Calcified tissue international 105 (2) (2019)
Margherita Maioli, Maria Gnoli, Manila Boarini, Morena Tremosini, Anna Zambrano, Elena Pedrini, Marina Mordenti, Serena Corsini, Patrizia D'Eufemia, Paolo Versacci, Mauro Celli, Luca Sangiorgi
Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients. European journal of human genetics : EJHG 27 (7) (2019)