Gnoli M - Search Results

1

Familiar osteopoikilosis: Case report with differential diagnosis and review of the literature.

Gaudio A, Xourafa A, Rapisarda R, Gorgone C, Gnoli M, Pedrini E, Sangiorgi L, Catalano A, Zanoli L, Mattina T, Castellino P. Gaudio A, et al. Among authors: gnoli m. Clin Case Rep. 2020 Dec 24;9(2):922-926. doi: 10.1002/ccr3.3611. eCollection 2021 Feb. Clin Case Rep. 2020. PMID: 33598273 Free PMC article.

2

Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?

Bozzola M, Gertosio C, Gnoli M, Baronio F, Pedrini E, Meazza C, Sangiorgi L. Bozzola M, et al. Among authors: gnoli m. Ital J Pediatr. 2015 Aug 4;41:53. doi: 10.1186/s13052-015-0162-2. Ital J Pediatr. 2015. PMID: 26239617 Free PMC article.

3

Evaluation of TP53 Pro72Arg and MDM2 SNP285-SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations.

Ponti F, Corsini S, Gnoli M, Pedrini E, Mordenti M, Sangiorgi L. Ponti F, et al. Among authors: gnoli m. Fam Cancer. 2016 Oct;15(4):635-43. doi: 10.1007/s10689-016-9895-3. Fam Cancer. 2016. PMID: 26956143

4

Tumor Syndromes That Include Bone Tumors: An Update.

Gnoli M, Ponti F, Sangiorgi L. Gnoli M, et al. Surg Pathol Clin. 2017 Sep;10(3):749-764. doi: 10.1016/j.path.2017.04.009. Surg Pathol Clin. 2017. PMID: 28797512 Review.

5

Insight into the Pathology of a COL1A1 Signal Peptide Heterozygous Mutation Leading to Severe Osteogenesis Imperfecta.

Lindert U, Gnoli M, Maioli M, Bedeschi MF, Sangiorgi L, Rohrbach M, Giunta C. Lindert U, et al. Among authors: gnoli m. Calcif Tissue Int. 2018 Mar;102(3):373-379. doi: 10.1007/s00223-017-0359-z. Epub 2017 Nov 3. Calcif Tissue Int. 2018. PMID: 29101475 Free PMC article.

6

Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients.

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. Maioli M, et al. Among authors: gnoli m. Eur J Hum Genet. 2019 Jul;27(7):1090-1100. doi: 10.1038/s41431-019-0373-x. Epub 2019 Mar 18. Eur J Hum Genet. 2019. PMID: 30886339 Free PMC article. Clinical Trial.

7

Melorheostosis and Osteopoikilosis Clinical and Molecular Description of an Italian Case Series.

Gnoli M, Staals EL, Campanacci L, Bedeschi MF, Faletra F, Gallone S, Gaudio A, Mattina T, Gurrieri F, Percesepe A, Neri I, Virdi A, Tremosini M, Milanesi A, Brizola E, Pedrini E, Sangiorgi L. Gnoli M, et al. Calcif Tissue Int. 2019 Aug;105(2):215-221. doi: 10.1007/s00223-019-00565-6. Epub 2019 May 25. Calcif Tissue Int. 2019. PMID: 31129707

8

Variable clinical expression of Stickler Syndrome: A case report of a novel COL11A1 mutation.

Brizola E, Gnoli M, Tremosini M, Nucci P, Bargiacchi S, La Barbera A, Giglio S, Sangiorgi L. Brizola E, et al. Among authors: gnoli m. Mol Genet Genomic Med. 2020 Sep;8(9):e1353. doi: 10.1002/mgg3.1353. Epub 2020 Jun 17. Mol Genet Genomic Med. 2020. PMID: 32558342 Free PMC article.

9

The natural history of multiple osteochondromas in a large Italian cohort of pediatric patients.

Mordenti M, Shih F, Boarini M, Pedrini E, Gnoli M, Antonioli D, Tremosini M, Sangiorgi L. Mordenti M, et al. Among authors: gnoli m. Bone. 2020 Oct;139:115499. doi: 10.1016/j.bone.2020.115499. Epub 2020 Jun 24. Bone. 2020. PMID: 32592948 Free article.

10

Case of melorheostosis associated with ipsilateral verrucous epidermal nevus, linear connective tissue nevus, diffuse hyperpigmentation and hypertrichosis: A fortuitous coincidence?

Di Altobrando A, Neri I, Gurioli C, Misciali C, Baraldi C, Pedrini E, Gnoli M, Tremosini M, Sangiorgi L, Patrizi A. Di Altobrando A, et al. Among authors: gnoli m. J Dermatol. 2020 Sep;47(9):1063-1066. doi: 10.1111/1346-8138.15460. Epub 2020 Jul 12. J Dermatol. 2020. PMID: 32656852

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