Trevisi P - Search Results

1

Molecular epidemiology of Usher syndrome in Italy.

Vozzi D, Aaspõllu A, Athanasakis E, Berto A, Fabretto A, Licastro D, Külm M, Testa F, Trevisi P, Vahter M, Ziviello C, Martini A, Simonelli F, Banfi S, Gasparini P. Vozzi D, et al. Among authors: trevisi p. Mol Vis. 2011;17:1662-8. Epub 2011 Jun 22. Mol Vis. 2011. PMID: 21738395 Free PMC article.

2

Vestibular anomalies and dysfunctions in children with inner ear malformations: A narrative review.

Brotto D, Ariano M, Sozzi M, Cenedese R, Muraro E, Sorrentino F, Trevisi P. Brotto D, et al. Among authors: trevisi p. Front Pediatr. 2023 Feb 27;11:1027045. doi: 10.3389/fped.2023.1027045. eCollection 2023. Front Pediatr. 2023. PMID: 36923273 Free PMC article. Review.

3

Exploring the clinical and epidemiological complexity of GJB2-linked deafness.

Gualandi F, Ravani A, Berto A, Sensi A, Trabanelli C, Falciano F, Trevisi P, Mazzoli M, Tibiletti MG, Cristofari E, Burdo S, Ferlini A, Martini A, Calzolari E. Gualandi F, et al. Among authors: trevisi p. Am J Med Genet. 2002 Sep 15;112(1):38-45. doi: 10.1002/ajmg.10621. Am J Med Genet. 2002. PMID: 12239718

4

Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele.

Gualandi E, Ravani A, Berto A, Burdo S, Trevisi P, Ferlini A, Martini A, Calzolari E. Gualandi E, et al. Among authors: trevisi p. Acta Otolaryngol Suppl. 2004 May;(552):29-34. doi: 10.1080/03655230410017166. Acta Otolaryngol Suppl. 2004. PMID: 15219044

5

Rehabilitation and outcome of severe profound deafness in a group of 16 infants affected by congenital cytomegalovirus infection.

Ciorba A, Bovo R, Trevisi P, Bianchini C, Arboretti R, Martini A. Ciorba A, et al. Among authors: trevisi p. Eur Arch Otorhinolaryngol. 2009 Oct;266(10):1539-46. doi: 10.1007/s00405-009-0944-5. Epub 2009 Mar 13. Eur Arch Otorhinolaryngol. 2009. PMID: 19283400

6

Hearing threshold assessment in young children with electrocochleography (EcochG) and auditory brainstem responses (ABR): experience at the University Hospital of Ferrara.

Aimoni C, Ciorba A, Bovo R, Trevisi P, Busi M, Martini A. Aimoni C, et al. Among authors: trevisi p. Auris Nasus Larynx. 2010 Oct;37(5):553-7. doi: 10.1016/j.anl.2010.02.002. Epub 2010 Mar 1. Auris Nasus Larynx. 2010. PMID: 20189737

7

Five new OTOF gene mutations and auditory neuropathy.

Zadro C, Ciorba A, Fabris A, Morgutti M, Trevisi P, Gasparini P, Martini A. Zadro C, et al. Among authors: trevisi p. Int J Pediatr Otorhinolaryngol. 2010 May;74(5):494-8. doi: 10.1016/j.ijporl.2010.02.004. Epub 2010 Mar 7. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20211493

8

LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations.

Sensi A, Ceruti S, Trevisi P, Gualandi F, Busi M, Donati I, Neri M, Ferlini A, Martini A. Sensi A, et al. Among authors: trevisi p. Am J Med Genet A. 2011 May;155A(5):1096-101. doi: 10.1002/ajmg.a.33962. Epub 2011 Apr 7. Am J Med Genet A. 2011. PMID: 21480479

9

Novel mutations in the SLC26A4 gene.

Busi M, Castiglione A, Taddei Masieri M, Ravani A, Guaran V, Astolfi L, Trevisi P, Ferlini A, Martini A. Busi M, et al. Among authors: trevisi p. Int J Pediatr Otorhinolaryngol. 2012 Sep;76(9):1249-54. doi: 10.1016/j.ijporl.2012.05.014. Epub 2012 Jun 18. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22717225

10

[Permanent childhood hearing impairment: universal newborn hearing screening, PCHI management].

Martini A, Marchisio P, Bubbico L, Trevisi P, Perletti L. Martini A, et al. Among authors: trevisi p. Minerva Pediatr. 2013 Apr;65(2):231-50. Minerva Pediatr. 2013. PMID: 23612271 Review. Italian.

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