Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Elisabetta Beatrice Nacci"'
Autor:
Raffaele Parrozzani, Elisabetta Beatrice Nacci, Silvia Bini, Giulia Marchione, Sabrina Salvadori, Daniel Nardo, Edoardo Midena
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
Abstract Pathophysiology of retinopathy of prematurity (ROP) still presents a gap. Lately blood tests parameters of premature infants have been measured at different times of ROP, attempting to detect correlations with ROP development and progression
Externí odkaz:
https://doaj.org/article/c78f830710c7427a9831738a6f8bc7c7
Autor:
Elisabetta Pilotto, Elisabetta Beatrice Nacci, Gilda De Mojà, Alfonso Massimiliano Ferrara, Raffaele Parrozzani, Davide Londei, Stefania Zovato, Edoardo Midena
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
Abstract Von Hippel–Lindau (VHL) disease is an autosomal dominant genetic disease caused by VHL gene mutation. Retinal hemangioblastomas (RH) are vascularized tumors and represent the main ocular manifestation of the disease. Histopathologically, R
Externí odkaz:
https://doaj.org/article/d8ff259dfa9a49869002046f785b0e17
Autor:
Eva Trevisson, Elisabetta Pilotto, Francesca Guidolin, Evelyn Longhin, Elisabetta Beatrice Nacci, Edoardo Midena
Publikováno v:
European Journal of Ophthalmology. 32:NP1-NP5
Background: Oguchi disease is a rare autosomal recessive retinal dystrophy, characterized by congenital stationary blindness and caused by pathogenic variants in SAG and GRK1 genes. The present study aimed to report an Italian patient affected by Ogu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c43b845c79f6d6f33ebda7a791ff9b29
https://doi.org/10.1177/11206721211027422
https://doi.org/10.1177/11206721211027422
Autor:
Elisabetta, Pilotto, Eva, Trevisson, Elisabetta Beatrice, Nacci, Evelyn, Longhin, Francesca, Guidolin, Edoardo, Midena
Publikováno v:
European journal of ophthalmology. 32(6)
Oguchi disease is a rare autosomal recessive retinal dystrophy, characterized by congenital stationary blindness and caused by pathogenic variants inA 60-year-old female complaining congenital stationary night blindness was investigated through fundu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec592c92ff7a142f58bd15b4b0d4054c
https://pubmed.ncbi.nlm.nih.gov/34162253
https://pubmed.ncbi.nlm.nih.gov/34162253
Autor:
Gilda De Mojà, Elisabetta Pilotto, Davide Londei, Raffaele Parrozzani, Elisabetta Beatrice Nacci, Stefania Zovato, Alfonso Massimiliano Ferrara, Edoardo Midena
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
Von Hippel–Lindau (VHL) disease is an autosomal dominant genetic disease caused by VHL gene mutation. Retinal hemangioblastomas (RH) are vascularized tumors and represent the main ocular manifestation of the disease. Histopathologically, RH are com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81beca9866106093a483045813e41e05
https://hdl.handle.net/11577/3379233
https://hdl.handle.net/11577/3379233
Autor:
Elisabetta Beatrice Nacci, Gilda De Mojà, Elisabetta Pilotto, Edoardo Midena, Stefania Zovato, Alfonso Massimiliano Ferrara
Publikováno v:
Journal of Clinical Medicine
Volume 9
Issue 8
Journal of Clinical Medicine, Vol 9, Iss 2677, p 2677 (2020)
Volume 9
Issue 8
Journal of Clinical Medicine, Vol 9, Iss 2677, p 2677 (2020)
Background: To evaluate macular perfusion in patients with Von Hippel&ndash
Lindau (VHL) disease. Methods: VHL patients with or without peripheral retinal hemangioblastomas (RHs) were consecutively enrolled. A group of healthy subjects served as
Lindau (VHL) disease. Methods: VHL patients with or without peripheral retinal hemangioblastomas (RHs) were consecutively enrolled. A group of healthy subjects served as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c0bace7ee66ef061ad22435ef16f7b3
Publikováno v:
Ophthalmic surgery, lasersimaging retina. 48(9)
Terson syndrome is defined as the incidence of intraocular hemorrhage in patients following a subarachnoid or intracranial bleed. A 38-year-old female with both intraretinal and subretinal hemorrhages secondary to Terson syndrome underwent repair of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c9a2fde3864576f6e287c3da8b784e2
https://pubmed.ncbi.nlm.nih.gov/28902339
https://pubmed.ncbi.nlm.nih.gov/28902339