Franzè A - Search Results

1

NeonaTal Assisted TelerehAbilitation (T.A.T.A. Web App) for Hearing-Impaired Children: A Family-Centered Care Model for Early Intervention in Congenital Hearing Loss.

Landolfi E, Continisio GI, Del Vecchio V, Serra N, Burattini E, Conson M, Marciano E, Laria C, Franzè A, Caso A, Fetoni AR, Malesci R. Landolfi E, et al. Among authors: franze a. Audiol Res. 2022 Mar 28;12(2):182-190. doi: 10.3390/audiolres12020021. Audiol Res. 2022. PMID: 35447741 Free PMC article.

2

Effect over time of allopurinol on noise-induced hearing loss in guinea pigs.

Franzé A, Sequino L, Saulino C, Attanasio G, Marciano E. Franzé A, et al. Int J Audiol. 2003 Jun;42(4):227-34. doi: 10.3109/14992020309101318. Int J Audiol. 2003. PMID: 12790348

3

Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families.

Di Leva F, D'Adamo AP, Strollo L, Auletta G, Caravelli A, Carella M, Mari F, Livi W, Renieri A, Gasparini P, D'Urso M, Marciano E, Franzé A. Di Leva F, et al. Among authors: franze a. Int J Audiol. 2003 Dec;42(8):475-80. doi: 10.3109/14992020309081517. Int J Audiol. 2003. PMID: 14658855

4

Down-regulation of otospiralin mRNA in response to acoustic stress in guinea pig.

Caravelli A, Pianese L, Saulino C, Di Leva F, Sequino L, Cocozza S, Marciano E, Franzé A. Caravelli A, et al. Among authors: franze a. Hear Res. 2004 Dec;198(1-2):36-40. doi: 10.1016/j.heares.2004.07.011. Hear Res. 2004. PMID: 15567600

5

Audiometric evaluation of carriers of the connexin 26 mutation 35delG.

Franzé A, Caravelli A, Di Leva F, Marciano E, Auletta G, D'Aulos F, Saulino C, Esposito L, Carella M, Gasparini P. Franzé A, et al. Eur Arch Otorhinolaryngol. 2005 Nov;262(11):921-4. doi: 10.1007/s00405-005-0918-1. Epub 2005 May 14. Eur Arch Otorhinolaryngol. 2005. PMID: 15895291

6

Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11).

Di Leva F, D'Adamo P, Cubellis MV, D'Eustacchio A, Errichiello M, Saulino C, Auletta G, Giannini P, Donaudy F, Ciccodicola A, Gasparini P, Franzè A, Marciano E. Di Leva F, et al. Among authors: franze a. Audiol Neurootol. 2006;11(3):157-64. doi: 10.1159/000091199. Epub 2006 Jan 9. Audiol Neurootol. 2006. PMID: 16449806

7

New evidence for the correlation of the p.G130V mutation in the GJB2 gene and syndromic hearing loss with palmoplantar keratoderma.

Iossa S, Chinetti V, Auletta G, Laria C, De Luca M, Rienzo M, Giannini P, Delfino M, Ciccodicola A, Marciano E, Franzé A. Iossa S, et al. Among authors: franze a. Am J Med Genet A. 2009 Feb 15;149A(4):685-8. doi: 10.1002/ajmg.a.32462. Am J Med Genet A. 2009. PMID: 18688874

8

Age-related hearing loss in four Italian genetic isolates: an epidemiological study.

Bedin E, Franzè A, Zadro C, Persico MG, Ciullo M, Hladnik U, Dolcetta D, Grasso DL, Riccardi P, Nutile T, Andrighetto G, D'Adamo P, Gasparini P, Marciano E. Bedin E, et al. Among authors: franze a. Int J Audiol. 2009;48(7):465-72. doi: 10.1080/14992020902822039. Int J Audiol. 2009. PMID: 19925333

9

Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss.

Chinetti V, Iossa S, Auletta G, Laria C, De Luca M, Di Leva F, Riccardi P, Giannini P, Gasparini P, Ciccodicola A, Marciano E, Franzè A. Chinetti V, et al. Among authors: franze a. Int J Audiol. 2010 Apr;49(4):326-31. doi: 10.3109/14992021003601756. Int J Audiol. 2010. PMID: 20233142

10

R75Q dominant mutation in GJB2 gene silenced by the in Cis recessive mutation c.35delG.

Iossa S, Chinetti V, Corvino V, Marciano E, Franzè A. Iossa S, et al. Among authors: franze a. Am J Med Genet A. 2010 Oct;152A(10):2658-60. doi: 10.1002/ajmg.a.33630. Am J Med Genet A. 2010. PMID: 20815033 No abstract available.

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