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

Author/Creator Testa, 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
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2. 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
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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
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4. 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
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5. 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
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6. 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
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7. 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
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