Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Vito Fenicia"'
Autor:
Giovanni Staurenghi, Francesco Bandello, Francesco Viola, Monica Varano, Giulia Barbati, Elena Peruzzi, Stefania Bassanini, Chiara Biancotto, Vito Fenicia, Claudio Furino, Maria Vadalà, Michele Reibaldi, Stela Vujosevic, Federico Ricci, EAGLE study investigators
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0256461 (2021)
ObjectiveTo assess the overall effectiveness of anti-vascular endothelial growth factor (VEGF) therapy in treatment-naïve patients with neovascular age-related macular degeneration (nAMD) in a clinical practice setting.Study designEAGLE was a retros
Externí odkaz:
https://doaj.org/article/7cd5ebd5d16f45ec8c3d063c3b733c62
Autor:
Andrea Maria Plateroti, Rocco Plateroti, Roberto Mollo, Aloisa Librando, Maria Teresa Contestabile, Vito Fenicia
Publikováno v:
Case Reports in Ophthalmology, Vol 8, Iss 2, Pp 375-384 (2017)
We present the case of a 12-year-old boy with Sturge-Weber syndrome and ocular melanocytosis who presented with bilateral naevus flammeus of the face and hyperpigmentation of the right iris associated with ipsilateral iris mammillations. The patient
Externí odkaz:
https://doaj.org/article/84d7b4834c71465da3df4df3f7a8301a
Autor:
Vito Fenicia, Marco Balestrieri, Andrea Perdicchi, Maurizio Maurizi Enrici, Martina Delle Fave, Santi Maria Recupero
Publikováno v:
Case Reports in Ophthalmology, Vol 5, Iss 2, Pp 243-248 (2014)
Purpose: To evaluate the efficacy of 2 dexamethasone intravitreal implants and 1 ranibizumab intravitreal injection after a bilateral postoperative complication of cataract surgery as pseudophakic cystoid macular edema. Patients and Methods: A 70-yea
Externí odkaz:
https://doaj.org/article/53d49796ebed46f1a21f656ff2f7f503
Publikováno v:
Case Reports in Ophthalmology, Vol 4, Iss 2, Pp 64-69 (2013)
Purpose: To evaluate the efficacy of one intravitreal injection of dexamethasone (Ozurdex®; Allergan, Inc., Irvine, Calif., USA) in serous macular detachment (SMD) of one eye, associated with bilateral central retinal vein occlusion (CRVO) in a pati
Externí odkaz:
https://doaj.org/article/559bc8b60fab41f1b86008b814f6021f
Autor:
Angela Ciarnella, Sara Verrilli, Vito Fenicia, Cristina Mannino, Alessandro Cutini, Andrea Perdicchi, Santi Maria Recupero
Publikováno v:
Case Reports in Ophthalmology, Vol 3, Iss 3, Pp 298-303 (2012)
Background: Idiopathic juxtafoveolar retinal telangiectasia (IJRT) type 1 represents an uncommon cause of congenital unilateral visual loss and it typically affects males. Decrease in visual acuity is caused by serous and lipid exudation into the fov
Externí odkaz:
https://doaj.org/article/e786bef35cd948cf96b600625a699147
Autor:
Federico Di Staso, Valeria Fameli, Gianluca Scuderi, Vito Fenicia, Federico Di Tizio, Solmaz Abdolrahimzadeh
Publikováno v:
Journal of Current Ophthalmology
Purpose: To report the effect of topical bromfenac, a non-steroidal anti-inflammatory drug (NSAID), in a case of neovascular age-related macular degeneration (AMD). Methods: An 85-year-old woman presented with a complaint of visual acuity reduction i
Publikováno v:
International Ophthalmology. 39:2851-2856
To assess safety and efficacy of deep topical anesthesia with ropivacaine-soaked sponge compared with topical anesthesia with oxybuprocaine in patients undergoing phacoemulsification. This was a retrospective study where records of patients operated
Autor:
Rocco Plateroti, Andrea Maria Plateroti, Vito Fenicia, Maria Teresa Contestabile, Roberto Mollo, Aloisa Librando
Publikováno v:
Case Reports in Ophthalmology, Vol 8, Iss 2, Pp 375-384 (2017)
Case Reports in Ophthalmology
Case Reports in Ophthalmology
We present the case of a 12-year-old boy with Sturge-Weber syndrome and ocular melanocytosis who presented with bilateral naevus flammeus of the face and hyperpigmentation of the right iris associated with ipsilateral iris mammillations. The patient
Autor:
Luca Scuderi, Maria Teresa Contestabile, Siavash Rahimi, Gianluca Scuderi, Vito Fenicia, Aloisa Librando
Publikováno v:
International ophthalmology. 39(7)
Pigment dispersion syndrome (PDS) is a condition where anomalous iridozonular contact leads to pigment dispersion throughout the anterior segment and the released pigment is abnormally deposited on various ocular structures. The clinical presentation
Autor:
Luca Scuderi, Vito Fenicia, Maria Teresa Contestabile, Siavash Rahimi, Gianluca Scuderi, Aloisa Librando
Publikováno v:
International Ophthalmology. 39:1663-1663
In the original publication, introduction section under Abstract was published incorrectly. The correct version is given below.