ritelli m - Search Results

Year	Number of Results
2003	1
2005	1
2006	1
2007	1
2008	1
2009	3
2010	1
2011	3
2012	5
2013	7
2014	9
2015	6
2016	11
2017	12
2018	12
2019	14
2020	10
2021	5
2022	6
2023	4
2024	7
2025	1

1

Molecular Genetics and Pathogenesis of Ehlers-Danlos Syndrome and Related Connective Tissue Disorders.

Ritelli M, Colombi M. Ritelli M, et al. Genes (Basel). 2020 May 13;11(5):547. doi: 10.3390/genes11050547. Genes (Basel). 2020. PMID: 32414079 Free PMC article.

2

Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type compared to other heritable connective tissue disorders.

Colombi M, Dordoni C, Chiarelli N, Ritelli M. Colombi M, et al. Among authors: ritelli m. Am J Med Genet C Semin Med Genet. 2015 Mar;169C(1):6-22. doi: 10.1002/ajmg.c.31429. Am J Med Genet C Semin Med Genet. 2015. PMID: 25821090 Review.

3

Bridging the Diagnostic Gap for Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders: Evidence of a Common Extracellular Matrix Fragmentation Pattern in Patient Plasma as a Potential Biomarker.

Ritelli M, Chiarelli N, Cinquina V, Bertini V, Piantoni S, Caproli A, Della Pina SEL, Franceschini F, Zarattini G, Gandy W, Venturini M, Zoppi N, Colombi M. Ritelli M, et al. Am J Med Genet A. 2025 Jan;197(1):e63857. doi: 10.1002/ajmg.a.63857. Epub 2024 Sep 3. Am J Med Genet A. 2025. PMID: 39225014

4

Genotypic Categorization of Loeys-Dietz Syndrome Based on 24 Novel Families and Literature Data.

Camerota L, Ritelli M, Wischmeijer A, Majore S, Cinquina V, Fortugno P, Monetta R, Gigante L, Marfan Syndrome Study Group Tor Vergata University Hospital, Sangiuolo FC, Novelli G, Colombi M, Brancati F. Camerota L, et al. Among authors: ritelli m. Genes (Basel). 2019 Sep 28;10(10):764. doi: 10.3390/genes10100764. Genes (Basel). 2019. PMID: 31569402 Free PMC article. Review.

5

Further Defining the Phenotypic Spectrum of B3GAT3 Mutations and Literature Review on Linkeropathy Syndromes.

Ritelli M, Cinquina V, Giacopuzzi E, Venturini M, Chiarelli N, Colombi M. Ritelli M, et al. Genes (Basel). 2019 Aug 21;10(9):631. doi: 10.3390/genes10090631. Genes (Basel). 2019. PMID: 31438591 Free PMC article. Review.

6

Current Evidence and Future Perspectives in the Medical Management of Vascular Ehlers-Danlos Syndrome: Focus on Vascular Prevention.

Buso G, Corvini F, Fusco EM, Messina M, Cherubini F, Laera N, Paini A, Salvetti M, De Ciuceis C, Ritelli M, Venturini M, Chiarelli N, Colombi M, Muiesan ML. Buso G, et al. Among authors: ritelli m. J Clin Med. 2024 Jul 21;13(14):4255. doi: 10.3390/jcm13144255. J Clin Med. 2024. PMID: 39064294 Free PMC article. Review.

7

Looking back and beyond the 2017 diagnostic criteria for hypermobile Ehlers-Danlos syndrome: A retrospective cross-sectional study from an Italian reference center.

Ritelli M, Chiarelli N, Cinquina V, Vezzoli M, Venturini M, Colombi M. Ritelli M, et al. Am J Med Genet A. 2024 Feb;194(2):174-194. doi: 10.1002/ajmg.a.63426. Epub 2023 Sep 29. Am J Med Genet A. 2024. PMID: 37774134

8

Despite celiprolol therapy, patients with vascular Ehlers-Danlos syndrome remain at risk of vascular events: A 12-year experience in an Italian referral center.

Buso G, Paini A, Agabiti-Rosei C, De Ciuceis C, Bertacchini F, Stassaldi D, Salvetti M, Ritelli M, Venturini M, Colombi M, Muiesan ML. Buso G, et al. Among authors: ritelli m. Vasc Med. 2024 Jun;29(3):265-273. doi: 10.1177/1358863X231215330. Epub 2023 Dec 16. Vasc Med. 2024. PMID: 38102934

9

Multifaced Roles of the αvβ3 Integrin in Ehlers-Danlos and Arterial Tortuosity Syndromes' Dermal Fibroblasts.

Zoppi N, Chiarelli N, Ritelli M, Colombi M. Zoppi N, et al. Among authors: ritelli m. Int J Mol Sci. 2018 Mar 26;19(4):982. doi: 10.3390/ijms19040982. Int J Mol Sci. 2018. PMID: 29587413 Free PMC article. Review.

10

Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes.

Chiarelli N, Ritelli M, Zoppi N, Colombi M. Chiarelli N, et al. Among authors: ritelli m. Genes (Basel). 2019 Aug 12;10(8):609. doi: 10.3390/genes10080609. Genes (Basel). 2019. PMID: 31409039 Free PMC article. Review.

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