Author/Creator: Simonelli, F - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Simonelli, F

1. 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) ↗

2. 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) ↗

3. 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) ↗

4. 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) ↗

5. 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) ↗

6. 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) ↗

7. A Martini coarse-grained model of the calcein fluorescent dye. (9th August 2018)

Authors:: Salassi, S; Simonelli, F; Bartocci, A; Rossi, G
Journal:: Journal of physics
Issue:: Volume 51:Number 38(2018)
Page Start:
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗