Search Results - "Miotto, Stefania"

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  1. 1

    Combined effects of genetic and non‐genetic risk factors affect response to ranibizumab in exudative age‐related macular degeneration by Piermarocchi, Stefano, Miotto, Stefania, Colavito, Davide, Leon, Alberta, Segato, Tatiana

    Published in Acta ophthalmologica (Oxford, England) (01-09-2015)
    “…Purpose To investigate whether genetic and non‐genetic risk factors influence 12‐month response to ranibizumab treatment for exudative age‐related macular…”
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    Quality of life impact of eye diseases: a Save Sight Registries study by Kandel, Himal, Nguyen, Vuong, Piermarocchi, Stefano, Ceklic, Lala, Teo, Kelvin, Arnalich‐Montiel, Francisco, Miotto, Stefania, Daien, Vincent, Gillies, Mark C., Watson, Stephanie L.

    Published in Clinical & experimental ophthalmology (01-05-2022)
    “…Background The objectives of this study were to evaluate the quality‐of‐life (QoL) impact of eye diseases (keratoconus; neovascular age‐related macular…”
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    Occult macular dystrophy in an Italian family carrying a mutation in the RP1L1 gene by PIERMAROCCHI, STEFANO, SEGATO, TATIANA, LEON, ALBERTA, COLAVITO, DAVIDE, MIOTTO, STEFANIA

    Published in Molecular medicine reports (01-03-2016)
    “…Occult macular dystrophy (OMD) is an inherited macular disease characterized by progressive visual decline with the absence of visible retinal abnormalities…”
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    Mitomycin C–Assisted Photorefractive Keratectomy in High Myopia: A Long-term Safety Study by Gambato, Catia, Miotto, Stefania, Cortese, Marta, Ghirlando, Alessandra, Lazzarini, Daniela, Midena, Edoardo

    Published in Cornea (01-06-2011)
    “…PURPOSE:To evaluate the long-term corneal safety of topical mitomycin C (MMC) used during photorefractive keratectomy to prevent haze formation in highly…”
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    Non-syndromic isolated dominant optic atrophy caused by the p.R468C mutation in the AFG3 like matrix AAA peptidase subunit 2 gene by Colavito, Davide, Maritan, Veronica, Suppiej, Agnese, Del Giudice, Elda, Mazzarolo, Monica, Miotto, Stefania, Farina, Sofia, Dalle Carbonare, Maurizio, Piermarocchi, Stefano, Leon, Alberta

    Published in Biomedical reports (01-11-2017)
    “…Autosomal dominant optic atrophy (DOA) is the most frequent form of hereditary optic atrophy, a disease presenting with considerable inter- and intra-familial…”
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    The Decreasing Prevalence of Nonrefractive Visual Impairment in Older Europeans by Le Goff, Mélanie, von Hanno, Therese, Mirshahi, Alireza, Anastosopoulos, Eleftherios, Cachulo, Maria Luz, Höhn, René, Wolfram, Christian, Miotto, Stefania, Carrière, Isabelle, Colijn, Johanna M., Buitendijk, Gabriëlle H.S., Evans, Jennifer, Nitsch, Dorothea, Founti, Panayiota, Yip, Jennifer L.Y., Pfeiffer, Norbert, Creuzot-Garcher, Catherine, Topouzis, Fotis, Bertelsen, Geir, Foster, Paul J., Fletcher, Astrid, Klaver, Caroline C.W., Korobelnik, Jean-François, Acar, Niyazi, Bergen, Arthur, Bertelsen, Geir, Binquet, Christine, Bird, Alan, Bobak, Martin, Boon, Camiel, Brétillon, Lionel, Bron, Alain, Capuano, Vittorio, Carrière, Isabelle, Chakravarthy, Usha, Chang, Petrus, Colijn, Johanna, Cougnard-Grégoire, Audrey, Cree, Angela, Creuzot-Garcher, Catherine, Cumberland, Phillippa, Cunha-Vaz, José, De Jong, Eiko, Deak, Gabor, Delcourt, Cécile, Dietzel, Martha, Finger, Robert, Fletcher, Astrid, Founti, Panayiota, Gorgels, Theo, Grauslund, Jakob, Grus, Franz, Helmer, Catherine, Hense, Hans-Werner, Hogg, Ruth, Holz, Frank, Hoyng, Carel, Janssen, Sarah, Khawaja, Anthony, Klaver, Caroline, Korobelnik, Jean-François, Le Goff, Mélanie, Lechanteur, Yara, Leung, Irene, Mauschitz, Matthias, Meester, Magda, Meyer zu Westrup, Verena, Midena, Edoardo, Miotto, Stefania, Mirshahi, Alireza, Muldrew, Alyson, Nickels, Stefan, Peto, Tunde, Pfeiffer, Norbert, Prokofyeva, Elena, Rahi, Jugnoo, Rauscher, Franziska, Rougier, Marie-Bénédicte, Rudnicka, Alicja, Sahel, José, Salonikiou, Aggeliki, Sanchez, Clarisa, Schmitz-Valckenberg, Steffen, Schouten, Johannes, Schuster, Alexander, Segato, Tatiana, Shehata, Jasmin, Silva, Rufino, Simader, Christian, Souied, Eric, Topouzis, Fotis, van Leeuwen, Elisa, Verzijden, Timo, Von Hanno, Therese, Vujosevic, Stela, Wiedemann, Peter, Williams, Katie, Wolfram, Christian, Yip, Jennifer, Zerbib, Jennyfer

    Published in Ophthalmology (Rochester, Minn.) (01-08-2018)
    “…To estimate the prevalence of nonrefractive visual impairment and blindness in European persons 55 years of age and older. Few visual impairment and blindness…”
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    Confocal microscopy of corneal sub-basal nerve plexus: a quantitative and qualitative analysis in healthy and pathologic eyes by Midena, Edoardo, Cortese, Marta, Miotto, Stefania, Gambato, Catia, Cavarzeran, Fabiano, Ghirlando, Alessandra

    Published in Journal of refractive surgery (1995) (01-01-2009)
    “…To validate corneal sub-basal nerve plexus examination by in vivo corneal confocal microscopy. Five parameters of corneal sub-basal nerve plexus in 250 human…”
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    Long-term effects on corneal keratocytes of mitomycin C during photorefractive keratectomy: a randomized contralateral eye confocal microscopy study by Midena, Edoardo, Gambato, Catia, Miotto, Stefania, Cortese, Marta, Salvi, Rudy, Ghirlando, Alessandra

    Published in Journal of refractive surgery (1995) (01-11-2007)
    “…To evaluate the long-term side effects of mitomycin C (MMC) assisted photorefractive keratectomy (PRK) on corneal keratocytes of highly myopic eyes…”
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  12. 12

    Long-term rearrangement of retinal structures in a novel mutation of X-linked retinoschisis by Piermarocchi, Stefano, Miotto, Stefania, Colavito, Davide, Del Giudice, Elda, Leon, Alberta, Maritan, Veronica, Piermarocchi, Rita, Tormene, Alma Patrizia

    Published in Biomedical reports (01-09-2017)
    “…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…”
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