Enrica Strettoi
Overview
Explore the profile of Enrica Strettoi including associated specialties, affiliations and a list of published articles.
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52
Citations
2293
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Recent Articles
1.
Napoli D, Orsini N, Salamone G, Calvello M, Capsoni S, Cattaneo A, et al.
eNeuro
. 2024 Sep;
11(9).
PMID: 39293937
Retinitis pigmentosa (RP) is a family of genetically heterogeneous diseases still without a cure. Despite the causative genetic mutation typically not expressed in cone photoreceptors, these cells inevitably degenerate following...
2.
Latini L, Souza Monteiro de Araujo D, Amato R, Canovai A, Buccarello L, De Logu F, et al.
Br J Pharmacol
. 2024 Sep;
181(23):4890-4919.
PMID: 39252503
Background And Purpose: Retinal ganglion cells (RGCs) are the output stage of retinal information processing, via their axons forming the optic nerve (ON). ON damage leads to axonal degeneration and...
3.
Carullo G, Orsini N, Piano I, Pozzetti L, Papa A, Fontana A, et al.
J Med Chem
. 2024 Jul;
67(17):14946-14973.
PMID: 38961727
Inherited retinal diseases, which include retinitis pigmentosa, are a family of genetic disorders characterized by gradual rod-cone degeneration and vision loss, without effective pharmacological treatments. Experimental approaches aim to delay...
4.
Napoli D, Strettoi E
J Anat
. 2022 Apr;
243(2):223-234.
PMID: 35428980
Retinal pigment epithelium (RPE) is a specialized pigmented monolayer dedicated to retinal support and protection. Given the fact that photoreceptor outer segments are the primary energy resource of RPE metabolism,...
5.
Strettoi E, Marco B, Orsini N, Napoli D
Int J Mol Sci
. 2022 Feb;
23(3).
PMID: 35163059
Brain plasticity is a well-established concept designating the ability of central nervous system (CNS) neurons to rearrange as a result of learning, when adapting to changeable environmental conditions or else...
6.
Puglia C, Santonocito D, Romeo G, Intagliata S, Romano G, Strettoi E, et al.
Molecules
. 2021 Aug;
26(15).
PMID: 34361825
Lipid-based nanocarriers (LNs) have made it possible to prolong corneal residence time and improve the ocular bioavailability of ophthalmic drugs. In order to investigate how the LNs interact with the...
7.
Kilicarslan I, Zanetti L, Novelli E, Schwarzer C, Strettoi E, Koschak A
Sci Rep
. 2021 Jul;
11(1):15146.
PMID: 34312410
Retinitis Pigmentosa is a genetically heterogeneous, degenerative retinal disorder characterized by gradual dysfunction and death of photoreceptors, first rods and later cones, and progressive blindness. Studies suggested that application of...
8.
Napoli D, Biagioni M, Billeri F, Marco B, Orsini N, Novelli E, et al.
Int J Mol Sci
. 2021 Jun;
22(10).
PMID: 34065385
In retinitis pigmentosa (RP), one of many possible genetic mutations causes rod degeneration, followed by cone secondary death leading to blindness. Accumulating evidence indicates that rod death triggers multiple, non-cell-autonomous...
9.
Thompson D, Iannaccone A, Ali R, Arshavsky V, Audo I, Bainbridge J, et al.
Transl Vis Sci Technol
. 2020 Aug;
9(7):2.
PMID: 32832209
Major advances in the study of inherited retinal diseases (IRDs) have placed efforts to develop treatments for these blinding conditions at the forefront of the emerging field of precision medicine....
10.
Piano I, DAntongiovanni V, Novelli E, Biagioni M, Cas M, Paroni R, et al.
Front Neurosci
. 2020 May;
14:372.
PMID: 32435178
Tvrm4 mice, a model of autosomal dominant retinitis pigmentosa (RP), carry a mutation of Rhodopsin gene that can be activated by brief exposure to very intense light. Here, we test...