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F Simonelli

Showing results (31-40 of 60) with videos related to

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The British Journal of Ophthalmology|July 19, 2005
A novel mutation in the RDS gene in an Italian family with pattern dystrophyF Testa, V Marini, S Rossi, et al.
Respiratory Medicine|June 29, 2013
Development and validation of a claims-based prediction model for COPD severityDendy Macaulay, Shawn X Sun, Rachael A Sorg, et al.
Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)|January 1, 1991
Cataract risk factors: blood level of antioxidative vitamins, reduced glutathione and malondialdehyde in cataractous patientsT Libondi, C Costagliola, M Della Corte, et al.
Investigative Ophthalmology & Visual Science|March 11, 2000
New ABCR mutations and clinical phenotype in Italian patients with Stargardt diseaseF Simonelli, F Testa, G de Crecchio, et al.
European Journal of Ophthalmology|October 25, 2006
Clinical phenotype of an Italian family with a new mutation in the PRPF8 geneF Testa, C Ziviello, M Rinaldi, et al.
Chronic Obstructive Pulmonary Diseases (Miami, Fla.)|August 7, 2025
Improving Research for COPD in Rural Areas: A Statement from the COPD Foundation Medical and Scientific Advisory CommitteeMaura E Thornton, David M Mannino, Jill A Ohar, et al.
Developments in Ophthalmology|January 1, 1989
Cataract formation in patients with lactose and galactose disordersF Simonelli, A Nesti, A Picardi, et al.
Ophthalmic Genetics|July 27, 1999
Retinal degeneration associated with ectopia lentisF Simonelli, G De Crecchio, F Testa, et al.
The British Journal of Ophthalmology|June 16, 2006
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian populationF Simonelli, G Frisso, F Testa, et al.
The British Journal of Ophthalmology|November 3, 1998
Ocular signs associated with a rhodopsin mutation (Cys-167-->Arg) in a family with autosomal dominant retinitis pigmentosaF Simonelli, M Rinaldi, A Nesti, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
The British Journal of Ophthalmology|July 19, 2005
A novel mutation in the RDS gene in an Italian family with pattern dystrophyF Testa, V Marini, S Rossi, et al.
Respiratory Medicine|June 29, 2013
Development and validation of a claims-based prediction model for COPD severityDendy Macaulay, Shawn X Sun, Rachael A Sorg, et al.
Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)|January 1, 1991
Cataract risk factors: blood level of antioxidative vitamins, reduced glutathione and malondialdehyde in cataractous patientsT Libondi, C Costagliola, M Della Corte, et al.
Investigative Ophthalmology & Visual Science|March 11, 2000
New ABCR mutations and clinical phenotype in Italian patients with Stargardt diseaseF Simonelli, F Testa, G de Crecchio, et al.
European Journal of Ophthalmology|October 25, 2006
Clinical phenotype of an Italian family with a new mutation in the PRPF8 geneF Testa, C Ziviello, M Rinaldi, et al.
Chronic Obstructive Pulmonary Diseases (Miami, Fla.)|August 7, 2025
Improving Research for COPD in Rural Areas: A Statement from the COPD Foundation Medical and Scientific Advisory CommitteeMaura E Thornton, David M Mannino, Jill A Ohar, et al.
Developments in Ophthalmology|January 1, 1989
Cataract formation in patients with lactose and galactose disordersF Simonelli, A Nesti, A Picardi, et al.
Ophthalmic Genetics|July 27, 1999
Retinal degeneration associated with ectopia lentisF Simonelli, G De Crecchio, F Testa, et al.
The British Journal of Ophthalmology|June 16, 2006
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian populationF Simonelli, G Frisso, F Testa, et al.
The British Journal of Ophthalmology|November 3, 1998
Ocular signs associated with a rhodopsin mutation (Cys-167-->Arg) in a family with autosomal dominant retinitis pigmentosaF Simonelli, M Rinaldi, A Nesti, et al.
Pageof 6