1. A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene. Issue 11 (14th August 2008) Authors: Testa, F; Rossi, S; Passerini, I; Sodi, A; Di Iorio, V; Interlandi, E; Corte, M Della; Menchini, U; Rinaldi, E; Torricelli, F; Simonelli, F Journal: British journal of ophthalmology Issue: Volume 92:Issue 11(2008) Page Start: 1467 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel mutation in the RDS gene in an Italian family with pattern dystrophy. Issue 8 (15th July 2005) Authors: Testa, F; Marini, V; Rossi, S; Interlandi, E; Nesti, A; Rinaldi, M; Varano, M; Garré, C; Simonelli, F Journal: British journal of ophthalmology Issue: Volume 89:Issue 8(2005) Page Start: 1066 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients. Issue 3 (December 2015) Authors: Melillo, P; Orrico, A; Attanasio, M; Rossi, S; Pecchia, L; Chirico, F; Testa, F; Simonelli, F Journal: BMC medical informatics and decision making Issue: Volume 15:Issue 3(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families. Issue 9 (20th August 2003) Authors: Simonelli, F; Cennamo, G; Ziviello, C; Testa, F; de Crecchio, G; Nesti, A; Manitto, M P; Ciccodicola, A; Banfi, S; Brancato, R; Rinaldi, E Journal: British journal of ophthalmology Issue: Volume 87:Issue 9(2003) Page Start: 1130 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Evaluation of prognostic risk models for postoperative pulmonary complications in adult patients undergoing major abdominal surgery: a systematic review and international external validation cohort study. Issue 7 (July 2022) Authors: Kouli, O; Murray, V; Bhatia, S; Cambridge, WA; Kawka, M; Shafi, S; Knight, SR; Kamarajah, SK; McLean, KA; Glasbey, JC; Khaw, RA; Ahmed, W; Akhbari, M; Baker, D; Borakati, A; Mills, E; Thavayogan, R; Yasin, I; Raubenheimer, K; Ridley, W Journal: Lancet Issue: Volume 4:Issue 7(2022) Page Start: e520 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families. Issue 7 (1st July 2005) Authors: Ziviello, C; Simonelli, F; Testa, F; Anastasi, M; Marzoli, S B; Falsini, B; Ghiglione, D; Macaluso, C; Manitto, M P; Garrè, C; Ciccodicola, A; Rinaldi, E; Banfi, S Journal: Journal of medical genetics Issue: Volume 42:Issue 7(2005) Page Start: e47 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population. Issue 9 (14th June 2006) Authors: Simonelli, F; Frisso, G; Testa, F; di Fiore, R; Vitale, D F; Manitto, M P; Brancato, R; Rinaldi, E; Sacchetti, L Journal: British journal of ophthalmology Issue: Volume 90:Issue 9(2006) Page Start: 1142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗