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The Journal of Bone and Joint Surgery. American Volume|January 20, 2012
Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of "protective" and "risk" factorsElena Pedrini, Ivy Jennes, Morena Tremosini, et al.
Cancers|June 2, 2021
Clinical, Histological, and Molecular Features of Solitary Fibrous Tumor of Bone: A Single Institution Retrospective ReviewGiuseppe Bianchi, Debora Lana, Marco Gambarotti, et al.
American Journal of Medical Genetics. Part A|September 3, 2021
The Rizzoli Multiple Osteochondromas Classification revised: describing the phenotype to improve clinical practiceMarina Mordenti, Maria Gnoli, Manila Boarini, et al.
Orphanet Journal of Rare Diseases|February 23, 2022
Secondary peripheral chondrosarcoma arising in solitary osteochondroma: variables influencing prognosis and survivalAlberto Righi, Marina Pacheco, Stefania Cocchi, et al.
Human Mutation|June 25, 2005
Evaluation of the molecular mechanisms involved in the gain of function of a Li-Fraumeni TP53 mutationSilvia Capponcelli, Elena Pedrini, Maria Antonietta Cerone, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|March 8, 2024
Health-related quality of life and associated risk factors in patients with Multiple Osteochondromas: a cross-sectional studyManila Boarini, Morena Tremosini, Alessia Di Cecco, et al.
Bone|December 16, 2014
The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesisFederica Sgariglia, Elena Pedrini, Jonathan P Bradfield, et al.
Calcified Tissue International|May 27, 2019
Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case SeriesMaria Gnoli, Eric Lodewijk Staals, Laura Campanacci, et al.
BMC Bioinformatics|November 9, 2021
Laniakea@ReCaS: exploring the potential of customisable Galaxy on-demand instances as a cloud-based serviceMarco Antonio Tangaro, Pietro Mandreoli, Matteo Chiara, et al.
Plos Genetics|May 3, 2011
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndromeMargot E Bowen, Eric D Boyden, Ingrid A Holm, et al.
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