Zobrazeno 1 - 10
of 299
pro vyhledávání: '"Alessandro Lambiase"'
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:
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
Autor:
Fabiana Mallone, Ludovico Alisi, Luca Lucchino, Valerio Di Martino, Marcella Nebbioso, Marta Armentano, Alessandro Lambiase, Antonietta Moramarco
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 17, p 13481 (2023)
Neurofibromatosis type 1 (NF1) is a rare inherited neurocutaneous disorder with a major impact on the skin, nervous system and eyes. The ocular diagnostic hallmarks of this disease include iris Lisch nodules, ocular and eyelid neurofibromas, eyelid c
Externí odkaz:
https://doaj.org/article/a5948e8f0d9e4faf915845d4ce26d0f4
Autor:
Eustachio Attico, Giulia Galaverni, Andrea Torello, Elisa Bianchi, Susanna Bonacorsi, Lorena Losi, Rossella Manfredini, Alessandro Lambiase, Paolo Rama, Graziella Pellegrini
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 14, p 11522 (2023)
Total bilateral Limbal Stem Cell Deficiency is a pathologic condition of the ocular surface due to the loss of corneal stem cells. Cultivated oral mucosa epithelial transplantation (COMET) is the only autologous successful treatment for this patholog
Externí odkaz:
https://doaj.org/article/240917235a9d4de699fe96b2d2d92082
Autor:
Gianpaolo Zerbini, Silvia Maestroni, Letizia Leocani, Andrea Mosca, Michela Godi, Renata Paleari, Arianna Belvedere, Daniela Gabellini, Paola Tirassa, Valerio Castoldi, Ilaria Viganò, Silvia Galbiati, Valentina Turco, Alessandro Lambiase, Paolo Rama
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Specific and effective preventive treatment for diabetic retinopathy (DR) is presently unavailable, mostly because the early stages of the complication have been, until recently, poorly understood. The recent demonstration that the vascular phase of
Externí odkaz:
https://doaj.org/article/aa3e62fe4b6c49e9acc02bcd7081a9f7
Autor:
Marta Armentano, Luca Lucchino, Ludovico Alisi, Antonio Valerio Chicca, Valerio Di Martino, Emanuele Miraglia, Ludovico Iannetti, Anna Maria Comberiati, Sandra Giustini, Alessandro Lambiase, Antonietta Moramarco
Publikováno v:
Applied Sciences, Vol 13, Iss 10, p 6304 (2023)
Neurofibromatosis type 2 (NF2) is a genetically determined tumor-predisposing syndrome. Ocular manifestations include cataracts, epiretinal membranes, retinal hamartomas, optic disk gliomas, and optic nerve sheath meningiomas. Moreover, optic disk ed
Externí odkaz:
https://doaj.org/article/cd6703b80b1e4ad28f5fd05701290829