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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: malesci r. Audiol Res. 2022 Mar 28;12(2):182-190. doi: 10.3390/audiolres12020021. Audiol Res. 2022. PMID: 35447741 Free PMC article.
Feasibility and effectiveness of a population-based newborn hearing screening in an economically deprived region of Italy.
Pisacane A, Auletta G, Toscano F, Errichiello M, Barrier F, Riccardi P, Laria C, Malesci R, Continisio GI, Continisio P, Barruffo L, Franzè A, Marciano E. Pisacane A, et al. Among authors: malesci r. Int J Pediatr Otorhinolaryngol. 2013 Mar;77(3):329-33. doi: 10.1016/j.ijporl.2012.09.019. Epub 2013 Jan 26. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23357779
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: malesci r. Mol Cytogenet. 2015 Mar 20;8:18. doi: 10.1186/s13039-015-0120-0. eCollection 2015. Mol Cytogenet. 2015. PMID: 25821518 Free PMC article.
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss.
Franzè A, Esposito G, Di Domenico C, Iossa S, Sauchelli G, Fioretti T, Cavaliere M, Auletta G, Corvino V, Laria C, Malesci R, Marciano E, Salvatore F. Franzè A, et al. Among authors: malesci r. Clin Chem Lab Med. 2016 Sep 1;54(9):e259-63. doi: 10.1515/cclm-2015-1216. Clin Chem Lab Med. 2016. PMID: 26894580 No abstract available.
X-Linked Sensorineural Hearing Loss: A Literature Review.
Corvino V, Apisa P, Malesci R, Laria C, Auletta G, Franzé A. Corvino V, et al. Among authors: malesci r. Curr Genomics. 2018 Aug;19(5):327-338. doi: 10.2174/1389202919666171218163046. Curr Genomics. 2018. PMID: 30065609 Free PMC article. Review.
Novel USH1G homozygous variant underlying USH2-like phenotype of Usher syndrome.
D'Esposito F, Randazzo V, Cennamo G, Centore N, Maltese PE, Malesci R, D'Andrea L, Bertelli M, Marciano E, de Crecchio G, Pioppo A, Magli A, Cordeiro MF. D'Esposito F, et al. Among authors: malesci r. Eur J Ophthalmol. 2021 Mar;31(2):NP18-NP22. doi: 10.1177/1120672119879392. Epub 2019 Sep 30. Eur J Ophthalmol. 2021. PMID: 31566003
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