Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Antonella De Benedictis"'
Autor:
Settimio Rossi, Francesco Testa, Marcella Attanasio, Ada Orrico, Antonella de Benedictis, Michele Della Corte, Francesca Simonelli
Publikováno v:
Case Reports in Ophthalmology, Vol 3, Iss 3, Pp 410-417 (2012)
Purpose: To report on 4 patients affected by Stargardt’s disease (STGD) with fundus flavimaculatus (FFM) and ABCA4 gene mutation associated with subretinal fibrosis. Methods: Four patients with a diagnosis of STGD were clinically examined. All 4 ca
Externí odkaz:
https://doaj.org/article/1a25b3aee5004095a48059a741088631
Autor:
Paolo Melillo, Raffaella Brunetti-Pierri, Sandro Banfi, Valentina Di Iorio, Gennarfrancesco Iaccarino, Antonella De Benedictis, Francesca Simonelli, Marianthi Karali, Francesco Testa
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 1681, p 1681 (2021)
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 1681, p 1681 (2021)
Volume 22
Issue 4
Achromatopsia (ACHM) is a rare genetic disorder of infantile onset affecting cone photoreceptors. To determine the extent of progressive retinal changes in achromatopsia, we performed a detailed longitudinal phenotyping and genetic characterization o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac28ef3c4512fb217b6f0b03f6f4e6ed
https://pubmed.ncbi.nlm.nih.gov/33562422
https://pubmed.ncbi.nlm.nih.gov/33562422
Autor:
Paolo, Melillo, Antonella De Benedictis, Edoardo, Villani, Maria Concetta Ferraro, Iadanza, Ernesto, Monica, Gherardelli, Francesco, Testa, Sandro, Banfi, Paolo, Nucci, Francesca, Simonelli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1820::742cf7091aa1203acf2f4b8d830cfe16
http://hdl.handle.net/11365/1201454
http://hdl.handle.net/11365/1201454
Autor:
Paolo Nucci, Edoardo Villani, Maria Concetta Ferraro, Ernesto Iadanza, Paolo Melillo, Antonella De Benedictis, Francesco Testa, Francesca Simonelli, Monica Gherardelli, Sandro Banfi
Publikováno v:
IFMBE Proceedings ISBN: 9789811090226
Chromatic pupillometry is a relatively novel research tool for retinal function evaluation and may be an appropriate and easier way to diagnose and monitor inherited retinal diseases in paediatric population. Nevertheless, although the method is clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a95f86b99c62a70d1933823e844f658
https://doi.org/10.1007/978-981-10-9023-3_70
https://doi.org/10.1007/978-981-10-9023-3_70
Autor:
Ciro Costagliola, Antonella De Benedictis, Cesare Danesino, Flavia Chiosi, Elisabetta Buscarini, Antonio Porcellini, Michele Rinaldi
Publikováno v:
Ophthalmic Genetics. 32:12-17
BACKGROUND: Hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease) is an autosomal dominant vascular disorder characterized by severe and recurrent nosebleeds, muco-cutaneous telangiectasias, and, in some cases, life-threatening visceral a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5ae30dbda584c4c19fe8b3e0bbe93a8
https://doi.org/10.3109/13816810.2010.535891
https://doi.org/10.3109/13816810.2010.535891
Publikováno v:
Neural Networks. 5:433-439
In this paper a binary associative network model with minimal number of connections is examined and its microscopic dynamics exactly studied. The knowledge of its time behavior allows us to determine a learning rule which realizes a one-step recallin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc71aaf2d8acf68a7d635506de6d6d33
https://doi.org/10.1016/0893-6080(92)90005-4
https://doi.org/10.1016/0893-6080(92)90005-4