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Francesco Testa

Showing results (91-100 of 126) with videos related to

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Retina (Philadelphia, Pa.)|November 10, 2016
CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2AFrancesco Testa, Paolo Melillo, Crystel Bonnet, et al.
Molecular Vision|July 9, 2011
Molecular epidemiology of Usher syndrome in ItalyDiego Vozzi, Anu Aaspõllu, Emmanouil Athanasakis, et al.
Investigative Ophthalmology & Visual Science|September 3, 2025
Cystoid Macular Edema in Non-Syndromic Retinitis Pigmentosa: Associations With Causative Genes in a Large CohortFrancesco Testa, Marianthi Karali, Rosa Boccia, et al.
Journal of Clinical Medicine|June 13, 2025
Evaluation of Vitamin D and of Some Biomarkers of Bone Remodelling (CTX-1, Osteocalcin, BALP) in Subjects with Periapical Inflammatory Cysts: An Observational StudyAngela Pia Cazzolla, Vincenzo Brescia, Roberto Lovero, et al.
Investigative Ophthalmology & Visual Science|April 9, 2011
Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapyFrancesco Testa, Enrico Maria Surace, Settimio Rossi, et al.
JMIR Medical Informatics|January 26, 2024
Ten Years of Experience With a Telemedicine Platform Dedicated to Health Care Personnel: Implementation ReportClaudio Azzolini, Elias Premi, Simone Donati, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patientsFrancesca Simonelli, Carmela Ziviello, Francesco Testa, et al.
BMC Medical Genetics|February 2, 2017
Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variantsGabriella Esposito, Francesco Testa, Miriam Zacchia, et al.
Orphanet Journal of Rare Diseases|July 31, 2023
A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practiceVittoria Murro, Sandro Banfi, Francesco Testa, et al.
Orphanet Journal of Rare Diseases|January 30, 2013
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophyIvana Peluso, Ivan Conte, Francesco Testa, et al.
Pageof 13

Showing results (91-100 of 126) with videos related to

Sort By:
Pageof 13
Retina (Philadelphia, Pa.)|November 10, 2016
CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2AFrancesco Testa, Paolo Melillo, Crystel Bonnet, et al.
Molecular Vision|July 9, 2011
Molecular epidemiology of Usher syndrome in ItalyDiego Vozzi, Anu Aaspõllu, Emmanouil Athanasakis, et al.
Investigative Ophthalmology & Visual Science|September 3, 2025
Cystoid Macular Edema in Non-Syndromic Retinitis Pigmentosa: Associations With Causative Genes in a Large CohortFrancesco Testa, Marianthi Karali, Rosa Boccia, et al.
Journal of Clinical Medicine|June 13, 2025
Evaluation of Vitamin D and of Some Biomarkers of Bone Remodelling (CTX-1, Osteocalcin, BALP) in Subjects with Periapical Inflammatory Cysts: An Observational StudyAngela Pia Cazzolla, Vincenzo Brescia, Roberto Lovero, et al.
Investigative Ophthalmology & Visual Science|April 9, 2011
Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapyFrancesco Testa, Enrico Maria Surace, Settimio Rossi, et al.
JMIR Medical Informatics|January 26, 2024
Ten Years of Experience With a Telemedicine Platform Dedicated to Health Care Personnel: Implementation ReportClaudio Azzolini, Elias Premi, Simone Donati, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patientsFrancesca Simonelli, Carmela Ziviello, Francesco Testa, et al.
BMC Medical Genetics|February 2, 2017
Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variantsGabriella Esposito, Francesco Testa, Miriam Zacchia, et al.
Orphanet Journal of Rare Diseases|July 31, 2023
A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practiceVittoria Murro, Sandro Banfi, Francesco Testa, et al.
Orphanet Journal of Rare Diseases|January 30, 2013
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophyIvana Peluso, Ivan Conte, Francesco Testa, et al.
Pageof 13