Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Veronica Maritan"'
Autor:
Agnese Suppiej, Silvia Marino, Maria Eleonora Reffo, Veronica Maritan, Giovanna Vitaliti, Janette Mailo, Raffaele Falsaperla
Publikováno v:
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-5 (2019)
Abstract Introduction Inherited retinal dystrophies are major cause of severe progressive vision loss in children. Early recognition and diagnosis are essential for timely visual rehabilitation during the appropriate stages of the visual development,
Externí odkaz:
https://doaj.org/article/9c26c190970b41b1ada76b1fc662c833
Autor:
Maria Eleonora Reffo, Giovanna Vitaliti, Janette Mailo, Agnese Suppiej, Veronica Maritan, Silvia Marino, Raffaele Falsaperla
Publikováno v:
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-5 (2019)
Italian Journal of Pediatrics
Italian Journal of Pediatrics
Introduction Inherited retinal dystrophies are major cause of severe progressive vision loss in children. Early recognition and diagnosis are essential for timely visual rehabilitation during the appropriate stages of the visual development, as well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90299f50bdb4c8045abb5cd4c372c552
https://doaj.org/article/9c26c190970b41b1ada76b1fc662c833
https://doaj.org/article/9c26c190970b41b1ada76b1fc662c833
Autor:
Davide Colavito, Alberta Leon, Rita Piermarocchi, Alma Patrizia Tormene, Stefano Piermarocchi, Elda Del Giudice, Veronica Maritan, Stefania Miotto
The aim of the present study was to report a novel mutation in the retinoschisin 1 (RS1) gene in a Caucasian family affected by X-linked juvenile retinoschisis (XLRS) and to describe the long-term modification of retinal structure. Two brothers with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27f755052b4c921cc34b61203faad140
http://hdl.handle.net/11577/3239842
http://hdl.handle.net/11577/3239842
Autor:
Davide Colavito, Elda Del Giudice, M. Mazzarolo, Veronica Maritan, Alberta Leon, Sofia Farina, Stefania Miotto, Stefano Piermarocchi, Maurizio Dalle Carbonare, Agnese Suppiej
Autosomal dominant optic atrophy (DOA) is the most frequent form of hereditary optic atrophy, a disease presenting with considerable inter- and intra-familial clinical variability. Although a number of mutations in different genes are now known to ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae95c6db44eb4083138548ce6266b82b
http://hdl.handle.net/11392/2387452
http://hdl.handle.net/11392/2387452
Autor:
Giuseppe Lo Giudice, Stefano Piermarocchi, Tatiana Segato, Veronica Maritan, Edoardo Midena, M. Sartore
Publikováno v:
Archives of ophthalmology (Chicago, Ill. : 1960). 126(10)
To evaluate the long-term effect of intravitreal triamcinolone acetonide (IVT) treatment combined with photodynamic therapy (PDT) vs PDT alone for neovascular age-related macular degeneration.Prospective randomized study. Eighty-four patients were en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a08b7b5af48b146ce08761948701e7e0
https://pubmed.ncbi.nlm.nih.gov/18852414
https://pubmed.ncbi.nlm.nih.gov/18852414
Autor:
Fabiano Cavarzeran, Iva Fregona, Enrica Convento, Maria Teresa Dorigo, Edoardo Midena, Veronica Maritan
To evaluate, with fundus perimetry, the peripapillary differential light threshold (DLT) in eyes with glaucoma and ocular hypertension (OHT), and compare it with peripapillary retinal nerve fibre layer (RNFL) thickness.35 glaucomatous, 29 OHT and 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::405e8a50e8f053a8b483be24caf30d85
http://hdl.handle.net/11577/2491863
http://hdl.handle.net/11577/2491863