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E Orzan

Showing results (21-30 of 28) with videos related to

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Journal of Medical Genetics|November 2, 1999
Cx26 deafness: mutation analysis and clinical variabilityA Murgia, E Orzan, R Polli, et al.
International Journal of Pediatric Otorhinolaryngology|May 14, 2013
Bilateral orbital preseptal cellulitis after combined adenotonsillectomy and strabismus surgery--case report and pathogenetic hypothesisE Muzzi, F Parentin, G Pelos, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|April 8, 2016
Achieving effective hearing aid fitting within one month after identification of childhood permanent hearing impairmentG Bastanza, R Gallus, M De Carlini, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 19, 2013
Failure of hearing screening in high-risk neonates does not increase parental anxietyA Suppiej, E Cainelli, M De Benedittis, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|April 8, 2016
Improving regional universal newborn hearing screening programmes in ItalyE Molini, M C Cristi, R Lapenna, et al.
Journal of Medical Genetics|February 27, 2004
A genotype-phenotype correlation for GJB2 (connexin 26) deafnessK Cryns, E Orzan, A Murgia, et al.
Journal of Medical Genetics|May 22, 2007
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentE Van Eyken, G Van Camp, E Fransen, et al.
B-ENT|January 30, 2008
Familial aggregation of tinnitus: a European multicentre studyJ J Hendrickx, J R Huyghe, K Demeester, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Journal of Medical Genetics|November 2, 1999
Cx26 deafness: mutation analysis and clinical variabilityA Murgia, E Orzan, R Polli, et al.
International Journal of Pediatric Otorhinolaryngology|May 14, 2013
Bilateral orbital preseptal cellulitis after combined adenotonsillectomy and strabismus surgery--case report and pathogenetic hypothesisE Muzzi, F Parentin, G Pelos, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|April 8, 2016
Achieving effective hearing aid fitting within one month after identification of childhood permanent hearing impairmentG Bastanza, R Gallus, M De Carlini, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 19, 2013
Failure of hearing screening in high-risk neonates does not increase parental anxietyA Suppiej, E Cainelli, M De Benedittis, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|April 8, 2016
Improving regional universal newborn hearing screening programmes in ItalyE Molini, M C Cristi, R Lapenna, et al.
Journal of Medical Genetics|February 27, 2004
A genotype-phenotype correlation for GJB2 (connexin 26) deafnessK Cryns, E Orzan, A Murgia, et al.
Journal of Medical Genetics|May 22, 2007
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentE Van Eyken, G Van Camp, E Fransen, et al.
B-ENT|January 30, 2008
Familial aggregation of tinnitus: a European multicentre studyJ J Hendrickx, J R Huyghe, K Demeester, et al.
Pageof 3