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Eva Orzan
Eva Orzan
Institute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy
在 burlo.trieste.it 的电子邮件经过验证 - 首页
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引用次数
引用次数
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GJB2 mutations and degree of hearing loss: a multicenter study
RL Snoeckx, PLM Huygen, D Feldmann, S Marlin, F Denoyelle, ...
The American Journal of Human Genetics 77 (6), 945-957, 2005
7002005
Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European …
E Fransen, V Topsakal, JJ Hendrickx, L Van Laer, JR Huyghe, ...
Journal of the Association for Research in Otolaryngology 9, 264-276, 2008
4052008
A genotype-phenotype correlation for GJB2 (connexin 26) deafness
K Cryns, E Orzan, A Murgia, PLM Huygen, F Moreno, I Del Castillo, ...
Journal of medical genetics 41 (3), 147-154, 2004
3222004
GRM7 variants confer susceptibility to age-related hearing impairment
RA Friedman, L Van Laer, MJ Huentelman, SS Sheth, E Van Eyken, ...
Human molecular genetics 18 (4), 785-796, 2009
2592009
Cx26 deafness: mutation analysis and clinical variability
A Murgia, E Orzan, R Polli, M Martella, C Vinanzi, E Leonardi, E Arslan, ...
Journal of medical genetics 36 (11), 829-832, 1999
2121999
The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment
L Van Laer, E Van Eyken, E Fransen, JR Huyghe, V Topsakal, ...
Human molecular genetics 17 (2), 159-169, 2008
1882008
Early primary cytomegalovirus infection in pregnancy: maternal hyperimmunoglobulin therapy improves outcomes among infants at 1 year of age
S Visentin, R Manara, L Milanese, A Da Roit, G Forner, E Salviato, ...
Clinical infectious diseases 55 (4), 497-503, 2012
1802012
Global problem of drug‐induced hearing loss
E Arslan, E Orzan, R Santarelli
Annals of the New York Academy of Sciences 884 (1), 1-14, 1999
1241999
Contribution of the N-acetyltransferase 2 polymorphism NAT2* 6A to age-related hearing impairment
E Van Eyken, G Van Camp, E Fransen, V Topsakal, JJ Hendrickx, ...
Journal of medical genetics 44 (9), 570-578, 2007
1172007
Reliability of hearing screening in high-risk neonates: comparative study of otoacoustic emission, automated and conventional auditory brainstem response
A Suppiej, E Rizzardi, V Zanardo, M Franzoi, M Ermani, E Orzan
Clinical Neurophysiology 118 (4), 869-876, 2007
952007
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait
JR Huyghe, L Van Laer, JJ Hendrickx, E Fransen, K Demeester, ...
The American Journal of Human Genetics 83 (3), 401-407, 2008
792008
The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss
E Van Eyken, L Van Laer, E Fransen, V Topsakal, JJ Hendrickx, ...
Otology & Neurotology 28 (7), 970-975, 2007
772007
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene
N Hilgert, MJ Huentelman, AQ Thorburn, E Fransen, N Dieltjens, ...
European journal of human genetics 17 (4), 517-524, 2009
652009
Molecular genetics applied to clinical practice: the Cx26 hearing impairment
E Orzan, R Polli, M Martella, C Vinanzi, M Leonardi, A Murgia
British journal of audiology 33 (5), 291-295, 1999
511999
Short report on the effects of SARS-CoV-2 face protective equipment on verbal communication
E Muzzi, C Chermaz, V Castro, M Zaninoni, A Saksida, E Orzan
European Archives of Oto-rhino-laryngology 278, 3565-3570, 2021
462021
Familial aggregation of tinnitus, a European multicentre study.
JJ Hendrickx, JR Huyghe, K Demeester, V Topsakal, E Van Eyken, ...
B ENT 2, 51-60, 2007
392007
A multicenter clinical evaluation of data logging in cochlear implant recipients using automated scene classification technologies
E Cristofari, D Cuda, A Martini, F Forli, D Zanetti, D Di Lisi, P Marsella, ...
Audiology and Neurotology 22 (4-5), 226-235, 2018
362018
Connexin 26 deafness is not always congenital
E Orzan, A Murgia
International journal of pediatric otorhinolaryngology 71 (3), 501-507, 2007
362007
Monitoring protocols for cochlear toxicity
SG Lord
Seminars in hearing 40 (02), 122-143, 2019
312019
Genomic studies in a large cohort of hearing impaired Italian patients revealed several new alleles, a rare case of uniparental disomy (UPD) and the importance to search for …
A Morgan, S Lenarduzzi, S Cappellani, V Pecile, M Morgutti, E Orzan, ...
Frontiers in Genetics 9, 681, 2018
292018
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