U
Umberto Ambrosetti
Researcher at Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
Publications - 74
Citations - 2248
Umberto Ambrosetti is an academic researcher from Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico. The author has contributed to research in topics: Hearing loss & Tinnitus. The author has an hindex of 24, co-authored 63 publications receiving 1914 citations. Previous affiliations of Umberto Ambrosetti include University of Milan.
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Journal ArticleDOI
GJB2 mutations and degree of hearing loss: a multicenter study.
Rikkert L. Snoeckx,Patrick L. M. Huygen,Delphine Feldmann,Sandrine Marlin,Françoise Denoyelle,Jaroslaw Waligora,Małgorzata Mueller-Malesińska,Agneszka Pollak,Rafał Płoski,Alessandra Murgia,Eva Orzan,Pierangela Castorina,Umberto Ambrosetti,Ewa Nowakowska-Szyrwinska,Jerzy Bal,Wojciech Wiszniewski,Andreas R. Janecke,Doris Nekahm-Heis,Pavel Seeman,O. Bendová,Margaret A. Kenna,Anna Frangulov,Heidi L. Rehm,Mustafa Tekin,Armagan Incesulu,Hans Henrik M. Dahl,Desirée du Sart,Lucy Jenkins,Deirdre Lucas,Maria Bitner-Glindzicz,Karen B. Avraham,Zippora Brownstein,Ignacio del Castillo,Felipe Moreno,Nikolaus Blin,Markus Pfister,István Sziklai,Tímea Tóth,Philip M. Kelley,Edward S. Cohn,Lionel Van Maldergem,Pascale Hilbert,Anne Françoise Roux,Michel Mondain,Lies H. Hoefsloot,Cor W. R. J. Cremers,Tuija Löppönen,Heikki Löppönen,Agnete Parving,Karen Grønskov,Iris Schrijver,Joseph B. Roberson,Francesca Gualandi,Alessandro Martini,Geneviève Lina-Granade,Nathalie Pallares-Ruiz,Céu Correia,Graça Fialho,Kim Cryns,Nele Hilgert,Paul Van de Heyning,Carla Nishimura,Richard J.H. Smith,Guy Van Camp +63 more
TL;DR: The association between genotype and degree of hearing loss in persons with HI and biallelic GJB2 mutations was assessed and two genotypes had significantly more-severe HI than that of 35delG homozygotes.
Journal ArticleDOI
A wider role for congenital cytomegalovirus infection in sensorineural hearing loss.
TL;DR: The results suggest that congenital CMV infection has a more relevant role in the etiology of SNHL than previously reported and suggest that 20 to 30% of all deafness cases are caused by CMV.
Journal ArticleDOI
A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy
Montserrat Rodríguez-Ballesteros,Raúl Reynoso,Margarita Olarte,Manuela Villamar,Constantino Morera,Rosamaria Santarelli,Edoardo Arslan,Carme Medá,Carlos Curet,C. Völter,Manuel Sainz-Quevedo,Pierangela Castorina,Umberto Ambrosetti,Stefano Berrettini,Klemens Frei,Socorro Tedín,Janine Smith,M. Cruz Tapia,Laura Cavallé,Nancy Gelvez,Paola Primignani,Elena Gómez-Rosas,Mirta Martín,M A Moreno-Pelayo,Martalucía Tamayo,José Moreno-Barral,Felipe Moreno,Ignacio del Castillo +27 more
TL;DR: The results confirm that mutation of the OTOF gene correlates with a phenotype of prelingual, profound NSHI, and indicate that OtoF mutations are a major cause of inherited auditory neuropathy.
Journal ArticleDOI
Questionnaires to evaluate anxiety and depressive levels in tinnitus patients
TL;DR: If a patient reports a THI greater than 38, the otolaryngologist should supplement diagnostic studies with a psychological consultation, and the same results were found with VAS.
Journal ArticleDOI
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing
Giulia Soldà,M. Robusto,Paola Primignani,Pierangela Castorina,Elena Benzoni,Antonio Cesarani,Antonio Cesarani,Umberto Ambrosetti,Umberto Ambrosetti,Rosanna Asselta,Stefano Duga +10 more
TL;DR: Further evidence of the involvement of miR-96 mutations in human deafness is provided and it is demonstrated that a quantitative defect of this miRNA may contribute to NSHL.