Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Marta Sacchetti"'
Autor:
Elizabeth Gavioli, Flavio Mantelli, Maria Candida Cesta, Marta Sacchetti, Marcello Allegretti
Publikováno v:
Biomolecules, Vol 14, Iss 6, p 635 (2024)
Nerve growth factor (NGF), the first neurotrophin to be discovered, has a long and eventful research journey with a series of turning points, setbacks, and achievements. Since the groundbreaking investigations led by Nobel Prize winner Rita Levi-Mont
Externí odkaz:
https://doaj.org/article/d884b4c79c3947508662f10af3af0b48
Autor:
Marco Marenco, Marco Segatto, Marta Sacchetti, Pietro Mangiantini, Francesca Giovannetti, Rocco Plateroti
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background Fabry disease (FD) is a rare X-linked, lysosomal storage disorder caused by mutations in the alpha-galactosidase gene and characterized by neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and ocular manifestation
Externí odkaz:
https://doaj.org/article/850892161d2c4fef9a2ab99e1a58f58c
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:
Antonietta Moramarco, Fabiana Mallone, Marta Sacchetti, Luca Lucchino, Emanuele Miraglia, Vincenzo Roberti, Alessandro Lambiase, Sandra Giustini
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Neurofibromatosis Type I (NF1), also termed von Recklinghausen disease, is a rare genetic disorder that is transmitted by autosomal dominant inheritance, with complete penetrance and variable expressivity. It is caused by mutation
Externí odkaz:
https://doaj.org/article/db034d03714547bebb25dfb43ea72a89
Autor:
Alessandro Lambiase, Marta Sacchetti, Fabiana Mallone, Paola Tirassa, Antonio Greco, Antonio Angeloni, Antonella Polimeni
Publikováno v:
Biomedicines, Vol 10, Iss 10, p 2430 (2022)
The waning effectiveness of the primary vaccination for SARS-CoV-2 led to administration of an additional booster dose (BD). The efficacy of the BD in stimulating humoral systemic immune response is well established, but its effectiveness on inducing
Externí odkaz:
https://doaj.org/article/61dd30b5d6e14770a4141ad68440cb81
Publikováno v:
Journal of Ophthalmology, Vol 2020 (2020)
Anterior capsule contraction syndrome (ACCS) is a rare, late complication of cataract surgery, associated with impairment of visual function. In this paper, we describe a new surgical technique to treat ACCS by femtosecond laser procedure. The femtos
Externí odkaz:
https://doaj.org/article/5e71cf883b18451e8e963d45bc7a2f1f
Publikováno v:
Life, Vol 11, Iss 10, p 1012 (2021)
Vernal keratoconjunctivitis (VKC) is a chronic, recurrent, inflammatory disease of the cornea and conjunctiva mostly affecting boys in prepubertal age. VKC recurrence is characterized by intense symptoms of itching, redness, and photophobia associate
Externí odkaz:
https://doaj.org/article/d9fdc2b8727e4f5aa4f010d73b89ea1f
Autor:
Marta Sacchetti, Alessandro Lambiase
Publikováno v:
Neural Regeneration Research, Vol 12, Iss 8, Pp 1220-1224 (2017)
The cornea has unique features that make it a useful model for regenerative medicine studies. It is an avascular, transparent, densely innervated tissue and any pathological changes can be easily detected by slit lamp examination. Corneal sensitivity
Externí odkaz:
https://doaj.org/article/84c7d70371f74f08bfdcfbd5b7b0ce6d
Autor:
Fabiana Mallone, Marta Sacchetti, Alice Bruscolini, Luca Scuderi, Marco Marenco, Alessandro Lambiase
Publikováno v:
Applied Sciences, Vol 10, Iss 24, p 9015 (2020)
Glaucoma is a neurodegenerative disease and a worldwide leading cause of irreversible vision loss. In the last decades, high efforts have been made to develop novel treatments effective in inducing protection and/or recovery of neural function in gla
Externí odkaz:
https://doaj.org/article/ec5a54ceee3041889eb84f77e75c07fe
Autor:
Rocco Plateroti, Marta Sacchetti, Giuseppe Magliulo, Andrea Maria Plateroti, Annalisa Pace, Antonietta Moramarco, Alessandro Lambiase, Alice Bruscolini
Publikováno v:
Life, Vol 10, Iss 9, p 202 (2020)
Background: patients with laryngopharyngeal reflux (LPR) showed detectable levels of tear pepsin that explain the nasolacrimal obstruction. The purpose of this study was to determine whether patients with LPR show ocular surface changes and to invest
Externí odkaz:
https://doaj.org/article/81f68ecc4c224e5686d43468000b3b19