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Author/Creator Ritelli, M.

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. 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) ↗

3. 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) ↗