Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Stanislao Rizzo"'
Autor:
Maria Cristina Savastano, Anna Rita Larici, Emanuele Crincoli, Alessandro De Filippis, Giuseppe Cicchetti, Gloria Gambini, Alfonso Savastano, Riccardo Marano, Luigi Natale, Stanislao Rizzo
Publikováno v:
European Journal of Ophthalmology. 32:3574-3583
Background Endothelium damage is a crucial element in the pathogenesis of SARS-Cov-2 infection. Most casualties in critical COVID-19 cases are due to ARDS, diffuse coagulopathy and cytokine storm. ARDS itself is a consequence of pulmonary endothelial
Autor:
Benedetto Falsini, Giorgio Placidi, Stanislao Rizzo, Grazia Maria Cozzupoli, E. De Siena, Andrea Giudiceandrea, A. Fadda, Tommaso Salgarello, Filippo Amore
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientific Reports
Scientific Reports
It has been previously demonstrated that the adaptive phase changes of steady-state pattern electroretinogram (SS-PERG), recorded during 4-min presentation of patterned stimuli, are reduced in glaucoma suspects and patients compared to normal subject
Autor:
Bianca Pacini, Stanislao Rizzo, Tomaso Caporossi, Lucia Finocchio, Ruggero Tartaro, Daniela Bacherini, Lorenzo De Angelis
Publikováno v:
Retina. 41:735-743
BACKGROUND/PURPOSE To determinate the efficacy of the human amniotic membrane plugs with sulfur hexafluoride versus human amniotic membrane plug with air as endotamponade to treat macular holes that failed to close after vitrectomy plus internal limi
Autor:
Stanislao Rizzo, Lucia Finocchio, Tomaso Caporossi, Bianca Pacini, Gianni Virgili, Ruggero Tartaro, Daniela Bacherini
Publikováno v:
Ophthalmology Retina. 4:996-1007
Purpose Age-related macular degeneration (AMD) is the leading cause of legal blindness in adults 65 years of age and older. Choroidal neovascularization (CNV) can complicate AMD and lead to severe visual acuity reduction. Despite the several treatmen
Autor:
Martina Maceroni, Stefano Maria Picardi, Stanislao Rizzo, Angelo Maria Minnella, Benedetto Falsini, Elisa De Siena, Giorgio Placidi
Publikováno v:
Advances in Therapy
Introduction Cataract surgery can be associated with vision-threatening complications in patients with diabetes. This study aimed to assess the functional and anatomic outcomes of the intravitreal dexamethasone (DEX) implant, administered at the time
Autor:
Stanislao Rizzo, Tomaso Caporossi, Lorenzo De Angelis, Francesco Barca, Bianca Pacini, Enrico Peiretti
Publikováno v:
Retina. 40:1946-1954
Purpose To assess the effectiveness of the human amniotic membrane plug for recurrent high myopic macular hole (MH) that already underwent pars plana vitrectomy with internal limiting membrane peeling and gas endotamponade. Methods Sixteen eyes of 16
Autor:
Andrea Sodi, Dario Giorgio, Ilaria Passerini, Gianni Virgili, Stanislao Rizzo, Elisabetta Pelo, Vittoria Murro, Dario Pasquale Mucciolo
Publikováno v:
Ophthalmic Genetics. 40:514-520
Purpose: To describe the outer retinal tubulation (ORT) morphology using En face OCT elaboration in a large group of patients affected by choroideremia (CHM).Material and Methods: We retrospectively reviewed CHM patients examined at the Regional Refe
Autor:
Giuseppe Roberto, Dario Pasquale Mucciolo, Michele Figus, Gianni Virgili, Gian Marco Tosi, Rosa Gini, Stanislao Rizzo, Vittoria Murro
Publikováno v:
European Journal of Ophthalmology. 30:1440-1447
Purpose: We aimed to develop indicators based on electronic administrative data to compare treatment intensity at a hospital level in Tuscany, Italy. Methods: Data from 3 university hospitals (UHs), 11 local hospitals (LHs) and 2 private hospitals we
Autor:
Lucia Finocchio, Ruggero Tartaro, Francesco Barca, Tomaso Caporossi, Stanislao Rizzo, Fabrizio Franco, Francesco Faraldi
Publikováno v:
Retina. 39:S151-S155
Autor:
Benedetto Falsini, Angelo Maria Minnella, Angela Romano, Mario Sabatelli, Martina Maceroni, Marco Luigetti, Romina Fasciani, Roberta Rissotto, Stanislao Rizzo
Publikováno v:
Genes
Genes, Vol 12, Iss 927, p 927 (2021)
Volume 12
Issue 6
Genes, Vol 12, Iss 927, p 927 (2021)
Volume 12
Issue 6
Hereditary transthyretin amyloidosis (hATTR) is a rare disease caused by a point mutation in the transthyretin (TTR) gene and inherited in an autosomal dominant fashion. TTR is a plasma protein that functions as a carrier for thyroxine (T4) and retin