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M Mazzoli

Research Profile

Disorders

Physiology

Concepts & Ideas

Genes & Molecular Sequences

Dominant Genes

Chemicals & Drugs

Procedures

Geographic Areas

Italy

Occupations

Audiology

Anatomy

Co-author Network

Publications

TOP 3
Andrea Ciorba; Stavros Hatzopoulos; Krzysztof Kochanek; M Mazzoli; A Pastore; Joseph Petruccelli; P Skarzynski; A Wlodarczyk; Henryk Skarzynski
Identifying congenital hearing impairment: preliminary results from a comparative study using objective and subjective audiometric protocols.
Elisabetta Flex; Massimo Mangino; M Mazzoli; martini alessandro; V Migliosi; Alessia Colosimo; Rita Mingarelli; Antonio Pizzuti; Bruno Dallapiccola
Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.
Francesca Gualandi; Anna Ravani; A Berto; Alberto Sensi; Cecilia Trabanelli; F Falciano; P Trevisi; M Mazzoli; M G Tibiletti; E Cristofari; S Burdo; Alessandra Ferlini; alessandro martini; Elisa Calzolari
Exploring the clinical and epidemiological complexity of GJB2-linked deafness.

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All Publications

2013: Andrea Ciorba; Stavros Hatzopoulos; Krzysztof Kochanek; M Mazzoli; A Pastore; Joseph Petruccelli; P Skarzynski; A Wlodarczyk; Henryk Skarzynski
Identifying congenital hearing impairment: preliminary results from a comparative study using objective and subjective audiometric protocols.
Acta otorhinolaryngologica Italica : organo ufficiale della Società italiana di otorinolaringologia e chirurgia cervico-facciale 2013;33(1):29-35.
2003: Elisabetta Flex; Massimo Mangino; M Mazzoli; martini alessandro; V Migliosi; Alessia Colosimo; Rita Mingarelli; Antonio Pizzuti; Bruno Dallapiccola
Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.
Journal of medical genetics 2003;40(4):278-81.
2002: Francesca Gualandi; Anna Ravani; A Berto; Alberto Sensi; Cecilia Trabanelli; F Falciano; P Trevisi; M Mazzoli; M G Tibiletti; E Cristofari; S Burdo; Alessandra Ferlini; alessandro martini; Elisa Calzolari
Exploring the clinical and epidemiological complexity of GJB2-linked deafness.
American journal of medical genetics 2002;112(1):38-45.
2001: alessandro martini; M Mazzoli; M Rosignoli; P Trevisi; S Maggi; G Enzi; G Crepaldi
Hearing in the elderly: a population study.
Audiology : official organ of the International Society of Audiology 2001;40(6):285-93.
2001: Massimo Mangino; Elisabetta Flex; Francesca Capon; Federica Sangiuolo; E Carraro; Francesca Gualandi; M Mazzoli; martini alessandro; Giuseppe Novelli; Bruno Dallapiccola
Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.
European journal of human genetics : EJHG 2001;9(9):667-71.
1998: Stavros Hatzopoulos; S Prosser; M Mazzoli; M Rosignoli; alessandro martini
Clinical applicability of transient evoked otoacoustic emissions: identification and classification of hearing loss.
Audiology & neuro-otology 1998;3(6):402-18.
1997: alessandro martini; M Milani; M Rosignoli; M Mazzoli; S Prosser
Audiometric patterns of genetic non-syndromal sensorineural hearing loss.
Audiology : official organ of the International Society of Audiology 1997;36(4):228-36.
1995: Stavros Hatzopoulos; M Mazzoli; alessandro martini
Identification of hearing loss using TEOAE descriptors: theoretical foundations and preliminary results.
Audiology : official organ of the International Society of Audiology 1995;34(5):248-59.
1983: W F Grigioni; A D'errico; M Mazzoli; M Milani; M Vanzo; V Villanacci; A Piccaluga
Mixed colonic polyposis.
Archives d'anatomie et de cytologie pathologiques 1983;31(6):359-62.