Trevisi P - Search Results

1

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

2

Hearing Aid in Vestibular-Schwannoma-Related Hearing Loss: A Review.

Di Pasquale Fiasca VM, Sorrentino F, Conti M, De Lucia G, Trevisi P, de Filippis C, Zanoletti E, Brotto D. Di Pasquale Fiasca VM, et al. Among authors: trevisi p. Audiol Res. 2023 Aug 8;13(4):627-635. doi: 10.3390/audiolres13040054. Audiol Res. 2023. PMID: 37622930 Free PMC article. Review.

3

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.

4

Improving Auditory Perception in Pediatric Single-Sided Deafness: Use of Cochlear Implants' Direct Connection for Remote Speech Perception Rehabilitation.

Agostinelli A, Pegolo M, Montino S, Maritan F, Gambalonga M, Trevisi P, Brotto D. Agostinelli A, et al. Among authors: trevisi p. Am J Audiol. 2023 Mar;32(1):52-58. doi: 10.1044/2022_AJA-21-00271. Epub 2022 Dec 20. Am J Audiol. 2023. PMID: 36538514

5

Branchio-oto (BO) syndrome and oculo-auriculo-vertebral phenotype: overlapping clinical findings in a child from a BO family.

Sensi A, Cocchi G, Martini A, Garani G, Trevisi P, Calzolari E. Sensi A, et al. Among authors: trevisi p. Clin Genet. 1996 Jun;49(6):300-2. doi: 10.1111/j.1399-0004.1996.tb03792.x. Clin Genet. 1996. PMID: 8884078

6

Hearing in the elderly: a population study.

Martini A, Mazzoli M, Rosignoli M, Trevisi P, Maggi S, Enzi G, Crepaldi G. Martini A, et al. Among authors: trevisi p. Audiology. 2001 Nov-Dec;40(6):285-93. Audiology. 2001. PMID: 11781040

7

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

8

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

9

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

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

180 results

Search Page

Filters