Zobrazeno 1 - 10
of 291
pro vyhledávání: '"ALESSANDRO LAMBIASE"'
Autor:
Danilo Iannetta, Vito Romano, Nicola Valsecchi, Arianna Grendele, Simone Febbraro, Marco Marenco, Antonio Moramarco, Alessandro Lambiase, Luigi Fontana
Publikováno v:
International Journal of Retina and Vitreous, Vol 10, Iss 1, Pp 1-6 (2024)
Abstract Background To assess anatomical and functional outcomes of retrolental cohesive ophthalmic viscoelastic injection (“Viscolift technique”) in patients with severely subluxated cataracts. Methods In the present prospective study, we includ
Externí odkaz:
https://doaj.org/article/e50ad6b54c75440686390cc5875a9ffc
Publikováno v:
PeerJ, Vol 12, p e17906 (2024)
Background Health literacy plays an important role in public health. Although this has been demonstrated in the field of ophthalmology, there are very few specific instruments available to assess eye health literacy. This work aims to develop an Ital
Externí odkaz:
https://doaj.org/article/ffbfee6965fa4c17ac7934c75b5b014c
Autor:
Valerio Di Martino, Fabiana Mallone, Alessandro Lambiase, Mauro Celli, Alice Mannocci, Luca Celli, Pietro Mangiantini, Pasquale Fino, Antonietta Moramarco
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Purpose Blue sclera is a characteristic and common clinical sign of Osteogenesis Imperfecta (OI). However, there is currently no widely accepted, objective method for assessing and grading blue sclera in individuals with OI. To address this
Externí odkaz:
https://doaj.org/article/6d2ef98797d14cce894ed3b6d9ce848d
Autor:
Marcella Nebbioso, Elvia Mastrogiuseppe, Eleonora Gnolfo, Marco Artico, Antonietta Moramarco, Fabiana Mallone, Samanta Taurone, Annarita Vestri, Alessandro Lambiase
Publikováno v:
Diagnostics, Vol 14, Iss 21, p 2409 (2024)
Objectives: Our objective was to investigate the prevalence of macular complications detected by spectral-domain optical coherence tomography (SD-OCT) in a large Caucasian cohort of RP patients, highlight the major alterations in chorioretinal struct
Externí odkaz:
https://doaj.org/article/95bd498e1fe94dff887d687a36e1a6d9
Autor:
Marta Armentano, Ludovico Alisi, Francesca Giovannetti, Valeria Iannucci, Luca Lucchino, Alice Bruscolini, Alessandro Lambiase
Publikováno v:
Life, Vol 14, Iss 8, p 1006 (2024)
Background: 22q11.2 deletion syndrome (22q11.2DS) is a genetic disorder caused by the deletion of the q11.2 band of chromosome 22. It may affect various systems, including the cardiovascular, immunological, gastrointestinal, endocrine, and neurocogni
Externí odkaz:
https://doaj.org/article/465a4bf2778245979a808df8b47ae4e2
Autor:
Valeria Iannucci, Alice Bruscolini, Giannicola Iannella, Giacomo Visioli, Ludovico Alisi, Mauro Salducci, Antonio Greco, Alessandro Lambiase
Publikováno v:
Biomedicines, Vol 12, Iss 5, p 1002 (2024)
Background: Olfactory dysfunction is a well-known phenomenon in neurological diseases with anosmia and hyposmia serving as clinical or preclinical indicators of Alzheimer’s disease, Parkinson’s disease, and other neurodegenerative disorders. Sinc
Externí odkaz:
https://doaj.org/article/4023f14360bc4111a44189be300291db
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-4 (2022)
Abstract Neurofibromatosis Type 1 (NF1) is a rare neurocutaneous disorder transmitted in an autosomal dominant fashion, mainly affecting the nervous system, the eye and skin. Ocular diagnostic hallmarks of NF1 include iris Lisch nodules, optic glioma
Externí odkaz:
https://doaj.org/article/48a4a25040074696b2923105f8b7fd4c
Autor:
Antonietta Moramarco, Luca Lucchino, Fabiana Mallone, Michela Marcelli, Ludovico Alisi, Vincenzo Roberti, Sandra Giustini, Alessandro Lambiase, Marcella Nebbioso
Publikováno v:
International Journal of Ophthalmology, Vol 15, Iss 5, Pp 773-779 (2022)
AIM: To examine neuroretinal function by using the multifocal electroretinography (mfERG) test in patients with neurofibromatosis type 1 (NF1) without optic pathway gliomas (OPGs). METHODS: This study was conducted on 35 patients (35 eyes) with NF1 a
Externí odkaz:
https://doaj.org/article/18b81dfe1e4e440ebb4b73a75702903e
Autor:
Alice Bruscolini, Marco Marenco, Giuseppe Maria Albanese, Alessandro Lambiase, Marta Sacchetti
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background Neurotrophic keratopathy (NK) is a rare, degenerative ocular disease characterized by reduction or loss of corneal sensitivity and development of non-healing corneal epithelial defects and ulcers. Cenegermin, a recombinant human n
Externí odkaz:
https://doaj.org/article/9794a878514a4a40b0bac2d2efc8a0e1
Autor:
Valeria Iannucci, Priscilla Manni, Ludovico Alisi, Giulia Mecarelli, Alessandro Lambiase, Alice Bruscolini
Publikováno v:
Life, Vol 13, Iss 9, p 1814 (2023)
Ocular trauma affects millions of people worldwide and is a leading cause of secondary glaucoma. Angle recession is the main cause of post-traumatic glaucoma after blunt eye trauma, and it is usually unilateral. The aim of this paper is to investigat
Externí odkaz:
https://doaj.org/article/232df6deb8ab4ff88cff76dd893ca0d4