Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Rocco Pio Ortore"'
Autor:
Rocco Pio Ortore, Maria Pia Leone, Orazio Palumbo, Antonio Petracca, Eleonora M. C. Trecca, Aurelio D’Ecclesia, Ciro Lucio Vigliaroli, Lucia Micale, Francesco Longo, Salvatore Melchionda, Marco Castori
Publikováno v:
Audiology Research, Vol 11, Iss 3, Pp 443-451 (2021)
Hearing loss (HL) affects 1–3 newborns per 1000 and, in industrialized countries, recognizes a genetic etiology in more than 80% of the congenital cases. Excluding GJB2 and GJB6, OTOA is one of the leading genes associated with autosomal recessive
Externí odkaz:
https://doaj.org/article/022434af817a417089d394876ba07f18
Autor:
Paola Tesolin, Anna Morgan, Michela Notarangelo, Rocco Pio Ortore, Maria Pina Concas, Angelantonio Notarangelo, Giorgia Girotto
Publikováno v:
Genes, Vol 12, Iss 7, p 1043 (2021)
Hearing loss (HL) is the most frequent sensory disorder, affecting about 1–3 per 1000 live births, with more than half of the cases attributable to genetic causes. Despite the fact that many HL causative genes have already been identified, current
Externí odkaz:
https://doaj.org/article/a2048f36046941dfb990362dc31c046e
Autor:
Francesco Longo, Aurelio D'Ecclesia, Marco Castori, Rocco Pio Ortore, Eleonora M C Trecca, Antonio Petracca, Salvatore Melchionda, Orazio Palumbo, Ciro Lucio Vigliaroli, Maria Pia Leone, Lucia Micale
Publikováno v:
Audiology Research
Audiology Research, Vol 11, Iss 41, Pp 443-451 (2021)
Audiology Research, Vol 11, Iss 41, Pp 443-451 (2021)
Hearing loss (HL) affects 1–3 newborns per 1000 and, in industrialized countries, recognizes a genetic etiology in more than 80% of the congenital cases. Excluding GJB2 and GJB6, OTOA is one of the leading genes associated with autosomal recessive
Autor:
Rocco Pio Ortore, Maria Pina Concas, Anna Morgan, Angelantonio Notarangelo, Paola Tesolin, Michela Notarangelo, Giorgia Girotto
Publikováno v:
Genes, Vol 12, Iss 1043, p 1043 (2021)
Genes
Genes
Hearing loss (HL) is the most frequent sensory disorder, affecting about 1–3 per 1000 live births, with more than half of the cases attributable to genetic causes. Despite the fact that many HL causative genes have already been identified, current
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2d3469ed25c6074e4b51eb97392d8f9
http://hdl.handle.net/11368/2993658
http://hdl.handle.net/11368/2993658
Autor:
Maria Pia Leone, Raffaella Stallone, Rocco Pio Ortore, Salvatore Melchionda, Roberto Cocchi, Massimo Carella, Pietro Palumbo, Tommaso Mazza, Teresa Palladino, Stefano Castellana, Orazio Palumbo
Publikováno v:
Molecular and Cellular Probes. 33:24-27
The paper describes a putative digenic form of deafness in two siblings affected by non-syndromic hereditary hearing loss, detected by a Targeted resequencing approach. Given that a previous paper suggested TMPRSS3 and GJB2 genes as responsible for a
Publikováno v:
Acta Oto-Laryngologica. 131:633-639
We question the justification for the cost of a surgically implanted device for the restoration of limited circumstances of audible communication, although we understand that the decision is taken depending on the social relevance of communication or
Publikováno v:
Europe PubMed Central
Objectives: We present a case of sudden bilateral profound deafness and vertigo, without any accompanying neurologic signs, secondary to bilateral infarctions of the cochlear and vestibular nuclei. Methods: Vertigo, vomiting, tinnitus, and bilateral