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Elio Marciano

Showing results (31-40 of 42) with videos related to

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Ophthalmic Genetics|July 14, 2017
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndromeFrancesco Testa, Paolo Melillo, Settimio Rossi, et al.
Audiology Research|April 21, 2022
NeonaTal Assisted TelerehAbilitation (T.A.T.A. Web App) for Hearing-Impaired Children: A Family-Centered Care Model for Early Intervention in Congenital Hearing LossEmma Landolfi, Grazia Isabella Continisio, Valeria Del Vecchio, et al.
International Journal of Pediatric Otorhinolaryngology|January 30, 2013
Feasibility and effectiveness of a population-based newborn hearing screening in an economically deprived region of ItalyAlfredo Pisacane, Gennaro Auletta, Fabiana Toscano, et al.
Clinical Chemistry and Laboratory Medicine|February 20, 2016
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing lossAnnamaria Franzè, Gabriella Esposito, Carmela Di Domenico, et al.
International Journal of Audiology|December 9, 2003
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian familiesFrancesca Di Leva, Adamo Pio D'Adamo, Luiaino Strollo, et al.
Audiology & Neuro-Otology|February 2, 2006
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11)Francesca Di Leva, Pio D'Adamo, Maria Vittoria Cubellis, et al.
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.
European Journal of Ophthalmology|October 1, 2019
Novel <i>USH1G</i> homozygous variant underlying USH2-like phenotype of Usher syndromeFabiana D'Esposito, Viviana Randazzo, Gilda Cennamo, et al.
International Journal of Audiology|November 21, 2009
Age-related hearing loss in four Italian genetic isolates: an epidemiological studyElisa Bedin, Annamaria Franzè, Cristina Zadro, 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.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Ophthalmic Genetics|July 14, 2017
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndromeFrancesco Testa, Paolo Melillo, Settimio Rossi, et al.
Audiology Research|April 21, 2022
NeonaTal Assisted TelerehAbilitation (T.A.T.A. Web App) for Hearing-Impaired Children: A Family-Centered Care Model for Early Intervention in Congenital Hearing LossEmma Landolfi, Grazia Isabella Continisio, Valeria Del Vecchio, et al.
International Journal of Pediatric Otorhinolaryngology|January 30, 2013
Feasibility and effectiveness of a population-based newborn hearing screening in an economically deprived region of ItalyAlfredo Pisacane, Gennaro Auletta, Fabiana Toscano, et al.
Clinical Chemistry and Laboratory Medicine|February 20, 2016
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing lossAnnamaria Franzè, Gabriella Esposito, Carmela Di Domenico, et al.
International Journal of Audiology|December 9, 2003
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian familiesFrancesca Di Leva, Adamo Pio D'Adamo, Luiaino Strollo, et al.
Audiology & Neuro-Otology|February 2, 2006
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11)Francesca Di Leva, Pio D'Adamo, Maria Vittoria Cubellis, et al.
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.
European Journal of Ophthalmology|October 1, 2019
Novel <i>USH1G</i> homozygous variant underlying USH2-like phenotype of Usher syndromeFabiana D'Esposito, Viviana Randazzo, Gilda Cennamo, et al.
International Journal of Audiology|November 21, 2009
Age-related hearing loss in four Italian genetic isolates: an epidemiological studyElisa Bedin, Annamaria Franzè, Cristina Zadro, 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.
Pageof 5