Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Enrico Fagnani"'
Autor:
Laura Pellegrinelli, Cristina Galli, Valeria Primache, Mirko Alde’, Enrico Fagnani, Federica Di Berardino, Diego Zanetti, Elena Pariani, Umberto Ambrosetti, Sandro Binda
Publikováno v:
BMC Infectious Diseases, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Congenital Cytomegalovirus (cCMV) is the most common cause of non-genetic hearing loss in childhood. A newborn hearing screening program (NHSP) is currently running in Italy, but no universal cCMV nor statewide hearing-targeted CM
Externí odkaz:
https://doaj.org/article/bd8dba5e74614df8b0faa22be4ca482d
Autor:
Federica Di Berardino, Cristina Galli, Umberto Ambrosetti, Diego Zanetti, Valeria Primache, Elena Pariani, Sandro Binda, Mirko Aldè, Enrico Fagnani, Laura Pellegrinelli
Publikováno v:
BMC Infectious Diseases
BMC Infectious Diseases, Vol 19, Iss 1, Pp 1-5 (2019)
BMC Infectious Diseases, Vol 19, Iss 1, Pp 1-5 (2019)
Background Congenital Cytomegalovirus (cCMV) is the most common cause of non-genetic hearing loss in childhood. A newborn hearing screening program (NHSP) is currently running in Italy, but no universal cCMV nor statewide hearing-targeted CMV screeni
Autor:
E. Filipponi, Antonio Cesarani, Elisabetta Iacona, C. Amadeo, Enrico Fagnani, E. Arisi, Stella Forti, Umberto Ambrosetti
Publikováno v:
Otology & Neurotology. 33:1113-1117
OBJECTIVE Several studies have demonstrated that adult subjects with Down's syndrome (DS) and hearing impairments show significantly delayed latencies in auditory late potentials (ALPs). The aim of this study was to investigate whether the difference
Autor:
Salvatore Cenzuales, Valeria Cuccarini, Umberto Ambrosetti, Bruno Mario Cesana, Alessandro Bottero, Pasquale Capaccio, Lorenzo Pignataro, Enrico Fagnani, Francesco Ottaviani
Publikováno v:
Genetics in Medicine. 7:206-208
Purpose: Sudden hearing loss (SHL) can be caused by vascular disorders favoring impaired cochlear perfusion. A number of inherited prothrombotic risk factors have been considered in the pathogenesis of vascular impairment and the possible role of gen
Autor:
Stella Forti, Umberto Ambrosetti, E. Filipponi, Enrico Fagnani, Antonio Cesarani, C. Amadeo, Lorenzo Pignataro
Publikováno v:
Brain research. 1233
Background: Auditory brainstem responses (ABRs) have been previously investigated in subjects with Down's syndrome (DS), but the published data are generally from children with hearing loss. The aim of this study was to evaluate the hearing pathway i
Autor:
Stella Forti, Giovanna Baracca, Umberto Ambrosetti, Alberto Scotti, Andrea Crocetti, Luca Del Bo, Enrico Fagnani
Publikováno v:
International journal of audiology. 46(5)
The aim of this study was to evaluate the efficacy of TRT in patients suffering from tinnitus. The tinnitus disorder affects about 10-15% of the population and, in one person out of a hundred, it is a disabling disorder. TRT treatment is based on Jas
Autor:
Valeria Cuccarini, Umberto Ambrosetti, Bruno Mario Cesana, Pasquale Capaccio, Lorenzo Pignataro, Alessandro Bottero, Salvatore Cenzuales, Enrico Fagnani, Francesco Ottaviani
Sudden hearing loss (SHL) can be caused by vascular disorders favoring impaired cochlear perfusion. Several inherited prothrombotic risk factors have been considered in the pathogenesis of vascular impairment, and the possible role of genetic alterat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fdb7632bb518b4905c743fa7ba3ad8b
http://hdl.handle.net/11379/19972
http://hdl.handle.net/11379/19972