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M R Pannarale

Showing results (11-20 of 21) with videos related to

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Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1980
[Blood-vitreous barrier under various experimental conditions]R Malagola, J Pecori-Giraldi, N Pellegrino, et al.
The British Journal of Ophthalmology|August 26, 1998
Plasma endothelin-1 concentrations in patients with retinal vein occlusionsA Iannaccone, C Letizia, S Pazzaglia, et al.
Acta Ophthalmologica Scandinavica|February 1, 1996
Electroretinographic alterations in the Laurence-Moon-Bardet-Biedl phenotypeA Iannaccone, E M Vingolo, E Rispoli, et al.
Acta Ophthalmologica Scandinavica|July 16, 1999
Treatment of nonproliferative diabetic retinopathy with Defibrotide in noninsulin-dependent diabetes mellitus: a pilot studyE M Vingolo, G De Mattia, C Giusti, et al.
Ophthalmic Genetics|March 1, 1997
The ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic retinitis pigmentosaA Iannaccone, G De Propris, S Roncati, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 1, 1995
Correlation between Goldmann perimetry and maximal electroretinogram response in retinitis pigmentosaA Iannaccone, E Rispoli, E M Vingolo, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 1, 1994
Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosisG Del Porto, E M Vingolo, K Steindl, et al.
Ophthalmology|September 1, 1996
Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observationsM R Pannarale, B Grammatico, A Iannaccone, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 1, 1997
Circulating endothelin-1 in non-insulin-dependent diabetic patients with retinopathyC Letizia, A Iannaccone, S Cerci, et al.
Journal of Medical Genetics|September 1, 1994
Autosomal dominant simple microphthalmosE M Vingolo, K Steindl, R Forte, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

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Pageof 3
Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1980
[Blood-vitreous barrier under various experimental conditions]R Malagola, J Pecori-Giraldi, N Pellegrino, et al.
The British Journal of Ophthalmology|August 26, 1998
Plasma endothelin-1 concentrations in patients with retinal vein occlusionsA Iannaccone, C Letizia, S Pazzaglia, et al.
Acta Ophthalmologica Scandinavica|February 1, 1996
Electroretinographic alterations in the Laurence-Moon-Bardet-Biedl phenotypeA Iannaccone, E M Vingolo, E Rispoli, et al.
Acta Ophthalmologica Scandinavica|July 16, 1999
Treatment of nonproliferative diabetic retinopathy with Defibrotide in noninsulin-dependent diabetes mellitus: a pilot studyE M Vingolo, G De Mattia, C Giusti, et al.
Ophthalmic Genetics|March 1, 1997
The ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic retinitis pigmentosaA Iannaccone, G De Propris, S Roncati, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 1, 1995
Correlation between Goldmann perimetry and maximal electroretinogram response in retinitis pigmentosaA Iannaccone, E Rispoli, E M Vingolo, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 1, 1994
Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosisG Del Porto, E M Vingolo, K Steindl, et al.
Ophthalmology|September 1, 1996
Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observationsM R Pannarale, B Grammatico, A Iannaccone, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 1, 1997
Circulating endothelin-1 in non-insulin-dependent diabetic patients with retinopathyC Letizia, A Iannaccone, S Cerci, et al.
Journal of Medical Genetics|September 1, 1994
Autosomal dominant simple microphthalmosE M Vingolo, K Steindl, R Forte, et al.
Pageof 3