Zobrazeno 1 - 10
of 281
pro vyhledávání: '"Benedetto Falsini"'
Publikováno v:
Optics, Vol 5, Iss 3, Pp 353-363 (2024)
Recovery after visual loss is a key goal of neuroscience and treatments able to improve visual function are still largely lacking. Glaucoma, one of the leading causes of visual disability in the world, is usually associated with elevated intraocular
Externí odkaz:
https://doaj.org/article/efb5742b4438444db9570d5d672bba02
Autor:
Stanislao Rizzo, MD, Maria Cristina Savastano, MD, PhD, Benedetto Falsini, MD, Patrizio Bernardinelli, MD, Francesco Boselli, MD, Umberto De Vico, MD, Matteo Mario Carlà, MD, Federico Giannuzzi, MD, Claudia Fossataro, MD, Gloria Gambini, MD, Emanuele Crincoli, MD, Silvia Ferrara, MD, Matteo Ripa, MD, Raphael Killian, MD, Clara Rizzo, MD, Caterina Giovanna Valentini, MD, PhD, Nicoletta Orlando, MSc, PhD, Giorgio Placidi, CO, Luciana Teofili, MD, PhD, Alfonso Savastano, MD, PhD
Publikováno v:
Ophthalmology Science, Vol 4, Iss 6, Pp 100476- (2024)
Purpose: To evaluate the safety of subretinal injection of cord blood platelet-rich plasma (CB-PRP) and its possible effect in eyes affected by geographic atrophy (GA) associated with dry age-related macular degeneration (d-AMD). Design: Intervention
Externí odkaz:
https://doaj.org/article/ea53d96b36dd4db78f9e9e164c4b4c1c
Autor:
Giorgio Placidi, Elena D’Agostino, Paolo Enrico Maltese, Maria Cristina Savastano, Gloria Gambini, Stanislao Rizzo, Gabriele Bonetti, Matteo Bertelli, Pietro Chiurazzi, Benedetto Falsini
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background This report presents a clinical case of syndromic rod-cone dystrophy due to a splice site variant in the ARL2BP gene causing situs inversus, asthenozoospermia, unilateral renal agenesis and microcysts. The presence of renal agenes
Externí odkaz:
https://doaj.org/article/1af6536faa4e4fd2b67af9635c62c787
Autor:
Marco Lombardo, Federico Ricci, Andrea Cusumano, Benedetto Falsini, Carlo Nucci, Massimo Cesareo
Publikováno v:
Diagnostics, Vol 14, Iss 20, p 2289 (2024)
Objectives: The main objective of this study was to report and investigate the characteristics and longitudinal changes in dark-without-pressure (DWP) fundus lesions in patients with autoimmune diseases using multimodal imaging techniques. Methods: I
Externí odkaz:
https://doaj.org/article/232c98cc588449b4b27eccd0efc7b558
Autor:
Andrea Cusumano, Benedetto Falsini, Michele D'Ambrosio, Fabian D'Apolito, Jacopo Sebastiani, Jung Hee Levialdi Ghiron, Emiliano Giardina, Raffaella Cascella
Publikováno v:
Case Reports in Ophthalmology, Vol 14, Iss 1, Pp 626-639 (2023)
Introduction: Doyne honeycomb retinal dystrophy (DHRD), or autosomal dominant radial drusen, is a genetic disease caused by pathogenic variants of the epidermal growth factor (EGF)-containing fibulin-like extracellular matrix protein 1 EFEMP1 gene an
Externí odkaz:
https://doaj.org/article/bcfe175132e64e98817868743e7b27e0
Autor:
Vittoria Murro, Sandro Banfi, Francesco Testa, Giancarlo Iarossi, Benedetto Falsini, Andrea Sodi, Sabrina Signorini, Achille Iolascon, Roberta Russo, Dario Pasquale Mucciolo, Roberto Caputo, Giacomo Maria Bacci, Sara Bargiacchi, Simona Turco, Stefania Fortini, Francesca Simonelli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-13 (2023)
Abstract Background Non-syndromic inherited retinal dystrophies (IRDs) such as retinitis pigmentosa or Leber congenital amaurosis generally manifest between early childhood and late adolescence, imposing profound long-term impacts as a result of visi
Externí odkaz:
https://doaj.org/article/e098df477d0641729cd2bab23f1352b6
Publikováno v:
Diagnostics, Vol 14, Iss 3, p 253 (2024)
This work aims to reveal the microscopic (2–3 micrometer resolution) appearance of human myelinated nerve fibers in vivo for the first time. We analyzed the myelinated retinal nerve fibers of a male patient without other neurological disorders in a
Externí odkaz:
https://doaj.org/article/3bf10fb42b85405d8510a67379f0f5d0
Autor:
Benedetto Falsini, Giorgio Placidi, Elisa De Siena, Pietro Chiurazzi, Angelo Maria Minnella, Maria Cristina Savastano, Lucia Ziccardi, Vincenzo Parisi, Giancarlo Iarossi, Marcella Percio, Barbora Piteková, Giuseppe Marceddu, Paolo Enrico Maltese, Matteo Bertelli
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Two-hundred and thirty-four Italian patients with a clinical diagnosis of macular, cone and cone-rod dystrophies (MD, CD, and CRD) were examined using next-generation sequencing (NGS) and gene sequencing panels targeting a specific set of ge
Externí odkaz:
https://doaj.org/article/10d57e6201e542a2bb031e010d0b5d5d
Autor:
Gabriele Bonetti, William Cozza, Andrea Bernini, Jurgen Kaftalli, Chiara Mareso, Francesca Cristofoli, Maria Chiara Medori, Leonardo Colombo, Salvatore Martella, Giovanni Staurenghi, Anna Paola Salvetti, Benedetto Falsini, Giorgio Placidi, Marcella Attanasio, Grazia Pertile, Mario Bengala, Francesca Bosello, Antonio Petracca, Fabiana D’Esposito, Benedetta Toschi, Paolo Lanzetta, Federico Ricci, Francesco Viola, Giuseppe Marceddu, Matteo Bertelli
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 23, p 16881 (2023)
Sequencing of the low-complexity ORF15 exon of RPGR, a gene correlated with retinitis pigmentosa and cone dystrophy, is difficult to achieve with NGS and Sanger sequencing. False results could lead to the inaccurate annotation of genetic variants in
Externí odkaz:
https://doaj.org/article/8eac08075aa14a4b977811dbf2dd789f
Autor:
Giuseppe Tringali, Michela Pizzoferrato, Lucia Lisi, Silvia Marinelli, Lucia Buccarello, Benedetto Falsini, Antonino Cattaneo, Pierluigi Navarra
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 22, p 16237 (2023)
In spite of its variety of biological activities, the clinical exploitation of human NGF (hNGF) is currently limited to ocular pathologies. It is therefore interesting to test the effects of hNGF in preclinical models that may predict their efficacy
Externí odkaz:
https://doaj.org/article/e6d46eaff75f47c6b88a8cf19a227fa3