Ciaccio, Claudia
Ciaccio, Claudia
Dipartimento di Medicina Molecolare e Traslazionale
Further delineation of FKBP14-related Ehlers-Danlos syndrome: a patient with early vascular complications and non-progressive kyphoscoliosis, and literature review
2016-01-01 Dordoni, Chiara; Ciaccio, Claudia; Venturini, Marina; CALZAVARA PINTON, Piergiacomo; Ritelli, Marco Giuseppe; Colombi, Marina
Koolen-de Vries Syndrome: Clinical Report of an Adult and Literature Review
2016-01-01 Ciaccio, Claudia; Dordoni, Chiara; Ritelli, Marco Giuseppe; Colombi, Marina
Marfan syndrome: Report of a complex phenotype due to a 15q21.1 contiguos gene deletion encompassing FBN1, and literature review
2017-01-01 Dordoni, Chiara; Ciaccio, Claudia; Santoro, Graziano; Venturini, Marina; Cavallari, Ugo; Ritelli, Marco Giuseppe; Colombi, Marina
Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients
2017-01-01 Colombi, M.; Dordoni, C.; Venturini, M.; Ciaccio, C.; Morlino, S.; Chiarelli, N.; Zanca, A.; Calzavara-Pinton, P.; Zoppi, N.; Castori, M.; Ritelli, M.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Further delineation of FKBP14-related Ehlers-Danlos syndrome: a patient with early vascular complications and non-progressive kyphoscoliosis, and literature review | 1-gen-2016 | Dordoni, Chiara; Ciaccio, Claudia; Venturini, Marina; CALZAVARA PINTON, Piergiacomo; Ritelli, Marco Giuseppe; Colombi, Marina | |
| Koolen-de Vries Syndrome: Clinical Report of an Adult and Literature Review | 1-gen-2016 | Ciaccio, Claudia; Dordoni, Chiara; Ritelli, Marco Giuseppe; Colombi, Marina | |
| Marfan syndrome: Report of a complex phenotype due to a 15q21.1 contiguos gene deletion encompassing FBN1, and literature review | 1-gen-2017 | Dordoni, Chiara; Ciaccio, Claudia; Santoro, Graziano; Venturini, Marina; Cavallari, Ugo; Ritelli, Marco Giuseppe; Colombi, Marina | |
| Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients | 1-gen-2017 | Colombi, M.; Dordoni, C.; Venturini, M.; Ciaccio, C.; Morlino, S.; Chiarelli, N.; Zanca, A.; Calzavara-Pinton, P.; Zoppi, N.; Castori, M.; Ritelli, M. |