Marciano E - Search Results

1

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: marciano e. Int J Audiol. 2003 Dec;42(8):475-80. doi: 10.3109/14992020309081517. Int J Audiol. 2003. PMID: 14658855

2

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. Among authors: marciano e. 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

3

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: marciano e. Audiol Neurootol. 2006;11(3):157-64. doi: 10.1159/000091199. Epub 2006 Jan 9. Audiol Neurootol. 2006. PMID: 16449806

4

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: marciano e. Int J Audiol. 2009;48(7):465-72. doi: 10.1080/14992020902822039. Int J Audiol. 2009. PMID: 19925333

5

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: marciano e. Int J Audiol. 2010 Apr;49(4):326-31. doi: 10.3109/14992021003601756. Int J Audiol. 2010. PMID: 20233142

6

Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme.

Chinetti V, Iossa S, Auletta G, Corvino V, De Luca M, De Falco F, Giannini P, Lilli G, Malesci R, Riccardi P, Marciano E, Franzè A. Chinetti V, et al. Among authors: marciano e. Int J Audiol. 2011 Dec;50(12):866-70. doi: 10.3109/14992027.2011.603757. Epub 2011 Sep 15. Int J Audiol. 2011. PMID: 21916817

7

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. Among authors: marciano e. Int J Audiol. 2003 Jun;42(4):227-34. doi: 10.3109/14992020309101318. Int J Audiol. 2003. PMID: 12790348

8

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: marciano e. 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

9

Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.

Iossa S, Costa V, Corvino V, Auletta G, Barruffo L, Cappellani S, Ceglia C, Cennamo G, D'Adamo AP, D'Amico A, Di Paolo N, Forte R, Gasparini P, Laria C, Lombardo B, Malesci R, Vitale A, Marciano E, Franzè A. Iossa S, et al. Among authors: marciano e. Mol Cytogenet. 2015 Mar 20;8:18. doi: 10.1186/s13039-015-0120-0. eCollection 2015. Mol Cytogenet. 2015. PMID: 25821518 Free PMC article.

10

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: marciano e. Hear Res. 2004 Dec;198(1-2):36-40. doi: 10.1016/j.heares.2004.07.011. Hear Res. 2004. PMID: 15567600

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