Enrica Strettoi

Affiliations: 
CNR, Pisa, Pisa, Toscana, Italy 
Area:
Visual System, Retina, Retinitis Pigmentosa
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"Enrica Strettoi"
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Publications

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Puglia C, Santonocito D, Romeo G, et al. (2021) Lipid Nanoparticles Traverse Non-Corneal Path to Reach the Posterior Eye Segment: In Vivo Evidence. Molecules (Basel, Switzerland). 26
Kilicarslan I, Zanetti L, Novelli E, et al. (2021) Knockout of Ca1.3 L-type calcium channels in a mouse model of retinitis pigmentosa. Scientific Reports. 11: 15146
Napoli D, Biagioni M, Billeri F, et al. (2021) Retinal Pigment Epithelium Remodeling in Mouse Models of Retinitis Pigmentosa. International Journal of Molecular Sciences. 22
Thompson DA, Iannaccone A, Ali RR, et al. (2020) Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium. Translational Vision Science & Technology. 9: 2
Piano I, D'Antongiovanni V, Novelli E, et al. (2020) Myriocin Effect on Tvrm4 Retina, an Autosomal Dominant Pattern of Retinitis Pigmentosa. Frontiers in Neuroscience. 14: 372
Stefanov A, Novelli E, Strettoi E. (2019) Inner Retinal Preservation in the photo-inducible I307N Rhodopsin Mutant Mouse, a Model of Autosomal Dominant Retinitis Pigmentosa. The Journal of Comparative Neurology
Testa G, Mainardi M, Morelli C, et al. (2019) The NGF mutation specifically impairs nociception without affecting cognitive performance in a mouse model of Hereditary Sensory and Autonomic Neuropathy type V. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Falasconi A, Biagioni M, Novelli E, et al. (2019) Retinal Phenotype in the rd9 Mutant Mouse, a Model of X-Linked RP. Frontiers in Neuroscience. 13: 991
Guadagni V, Biagioni M, Novelli E, et al. (2019) Rescuing cones and daylight vision in retinitis pigmentosa mice. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. fj201900414R
Lupori L, Sagona G, Fuchs C, et al. (2019) Site-specific abnormalities in the visual system of a mouse model of CDKL5 deficiency disorder. Human Molecular Genetics
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