1. A recognizable systemic connective tissue disorder with polyvalvular heart dystrophy and dysmorphism associated with TAB2 mutations. Issue 1 (21st August 2017) Authors: Ritelli, M.; Morlino, S.; Giacopuzzi, E.; Bernardini, L.; Torres, B.; Santoro, G.; Ravasio, V.; Chiarelli, N.; D'Angelantonio, D.; Novelli, A.; Grammatico, P.; Colombi, M.; Castori, M. Journal: Clinical genetics Issue: Volume 93:Issue 1(2018) Page Start: 126 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Comparison of Two Mechanics-Based Methods for Simplified Structural Analysis in Vulnerability Assessment. (30th June 2008) Authors: Crowley, H.; Borzi, B.; Pinho, R.; Colombi, M.; Onida, M. Other Names: Elnashai Amr Academic Editor. Journal: Advances in civil engineering Issue: Volume 2008(2008) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Compound heterozygosity of the novel −186C>T mutation in the COL7A1 promoter and the recurrent c.497insA mutation leads to generalized dystrophic epidermolysis bullosa. (31st January 2013) Authors: Ritelli, M.; Chiarelli, N.; Quinzani, S.; Dordoni, C.; Venturini, M.; Calzavara‐Pinton, P.; Colombi, M. Journal: British journal of dermatology Issue: Volume 168:Number 4(2013:Apr.) Page Start: 904 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers‐Danlos syndrome patients. Issue 6 (4th September 2017) Authors: Colombi, M.; Dordoni, C.; Venturini, M.; Ciaccio, C.; Morlino, S.; Chiarelli, N.; Zanca, A.; Calzavara‐Pinton, P.; Zoppi, N.; Castori, M.; Ritelli, M. Journal: Clinical genetics Issue: Volume 92:Issue 6(2017) Page Start: 624 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗