Pubblicazioni principali

1.    Maioli M, Gnoli M, Boarini M, Tremosini M, Zambrano A, Pedrini E, Mordenti M, Corsini S, D'Eufemia P, Versacci P, Celli M, Sangiorgi L. Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients. Eur J Hum Genet. 2019 Mar 18. doi: 10.1038/s41431-019-0373-x
2.    Sangiorgi L, Mordenti M. Disease Registry: A Tool for European Cross-Border Medicine. In Book: New Perspectives in Medical Records. TELe-Health Series. Springer International pp 141-152. 2017
3.    Gnoli M, Ponti F, Sangiorgi L. Tumor Syndromes That Include Bone Tumors: An Update. Surg Pathol Clin. 2017 Sep;10(3):749-764. doi: 10.1016/j.path.2017.04.009. Review.
4.    Ponti F, Corsini S, Gnoli M, Pedrini E, Mordenti M, Sangiorgi L. Evaluation of TP53 Pro72Arg and MDM2 SNP285–SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations. Fam. Canc. 2016.15: 4, 635-643

Contenuto aggiornato il 14/08/2019 - 17:58
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