Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Francesca Guidolin"'
Autor:
Francesca Guidolin, Valeria Tatano
Publikováno v:
Techne, Iss 11 (2016)
Gli skybridges, diffusisi negli ultimi vent’anni nelle città a sviluppo verticale, rappresentano una modalità di collegamento in quota tra edifici di grande altezza e costituiscono oggi una vera e propria infrastruttura urbana, essendo in grado d
Externí odkaz:
https://doaj.org/article/cfe63d8f012442d0baee4509ad766f77
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:
Fabio Sirchia, Ilaria Fantasia, Irene Della Pietà, Flavio Faletra, Francesca Guidolin, Mariachiara Quadrifoglio, Tamara Stampalija, Chiara Ottaviani Giammarco, Laura Travan, Valentina Barresi
Publikováno v:
Prenatal diagnosisREFERENCES. 40(12)
Objective: To evaluate the association of first-trimester absent nasal bone (NB) and genetic abnormalities at G-banding karyotype and chromosomal microarray analysis (CMA) according to the nuchal translucency (NT) thickness. Methods: This is a retros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60093f397d56557dd9a977a2b90d9bc0
https://pubmed.ncbi.nlm.nih.gov/32799336
https://pubmed.ncbi.nlm.nih.gov/32799336
Gene prioritization is the process of determining which variants and genes identified in genetic analyses are likely to cause a disease or a variation in a phenotype. For many genes, neither in vitro nor in vivo testing is available, thus assessing t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd035d3130599240cf929a390171d4c9
https://hdl.handle.net/11368/2964103
https://hdl.handle.net/11368/2964103
Autor:
Gianni Sorarù, Silvio C. E. Tosatto, Bruno F. Gavassini, Boris Pantic, Chiara Calore, Giovanna Cenacchi, Claudio Semplicini, Cinzia Bertolin, Maurizio Moggio, Francesca Guidolin, Giovanni Minervini, Elena Pegoraro, Roberto Stramare, Francesco Catapano, Luca Bello, Marco Previtero, Valentina Papa, Sara Vianello, Irene Colombo
Publikováno v:
Neurology. 91:e1629-e1641
ObjectiveTo identify and characterize patients with calsequestrin 1 (CASQ1)–related myopathy.MethodsPatients selected according to histopathologic features underwent CASQ1 genetic screening. CASQ1-mutated patients were clinically evaluated and unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c93abbcdb8ddee2c079b008d3e01d0d
https://doi.org/10.1212/wnl.0000000000006387
https://doi.org/10.1212/wnl.0000000000006387
Autor:
Edoardo Midena, Anna Rita Daniele, Raffaele Parrozzani, Luisa Frizziero, Elisabetta Pilotto, Evelyn Longhin, Fabiano Cavarzeran, Enrica Convento, Francesca Guidolin
AimsTo investigate, with optical coherence tomography angiography (OCTA), short-term changes of type 1 choroidal neovascularisation (CNV), secondary to exudative age-related macular degeneration, after anti-vascular endothelial growth factor (VEGF) t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88af6045bcf1256aaebd205cc9c50aa9
http://hdl.handle.net/11577/3269084
http://hdl.handle.net/11577/3269084
Autor:
Raffaele Parrozzani, Francesca Guidolin, Clelia Karine Abalsamo, Evelyn Longhin, Elisabetta Pilotto, Edoardo Midena, Enrica Convento
Importance Progressive geographic atrophy (GA) of the retinal pigment epithelium leads to loss of central vision. To identify GA in age-related macular degeneration and assess treatment, correlation of function observed on microperimetry with structu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a9b324a4f229aba1a249b20255c723b
http://hdl.handle.net/11577/3188212
http://hdl.handle.net/11577/3188212
Autor:
Raffaele Parrozzani, Elisabetta Pilotto, Edoardo Midena, Francesca Guidolin, Enrica Convento, Francesco Giuseppe Stefanon
Publikováno v:
The British journal of ophthalmology. 99(8)
Purpose To analyse changes in choroidal thickness and retinal sensitivity (Se) in patients with geographic atrophy (GA) with or without choroidal neovascularisation (CNV) in the fellow eye. Participants Patients with bilateral GA (B-GA group) and pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61845a2d68e7863c4617ed2631342aae
https://pubmed.ncbi.nlm.nih.gov/25677674
https://pubmed.ncbi.nlm.nih.gov/25677674
Microperimetry, fundus autofluorescence, and retinal layer changes in progressing geographic atrophy
Autor:
Evelyn Longhin, Edoardo Midena, Elisa Benetti, Raffaele Parrozzani, Enrica Convento, Francesca Guidolin, Elisabetta Pilotto
Publikováno v:
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie. 48(5)
To analyze correlation among microperimetry, inner and outer retinal layers, and fundus autofluorescence (FAF) changes in eyes with progressing geographic atrophy (GA) secondary to age-related macular degeneration.Microperimetry, spectral-domain opti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c0ac91d704020e051df1de12118ded7
https://pubmed.ncbi.nlm.nih.gov/24093185
https://pubmed.ncbi.nlm.nih.gov/24093185