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Page 1
Navigating the Usher Syndrome Genetic Landscape: An Evaluation of the Associations between Specific Genes and Quality Categories of Cochlear Implant Outcomes.
Audiol Res. 2024 Feb 26;14(2):254-263. doi: 10.3390/audiolres14020023.
Audiol Res. 2024.
PMID: 38525684
Free PMC article.
Review.
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.
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
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Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects.
Guaran V, Astolfi L, Castiglione A, Simoni E, Olivetto E, Galasso M, Trevisi P, Busi M, Volinia S, Martini A.
Guaran V, et al. Among authors: busi m.
Int J Mol Med. 2013 Oct;32(4):785-94. doi: 10.3892/ijmm.2013.1470. Epub 2013 Aug 16.
Int J Mol Med. 2013.
PMID: 23969527
Free PMC article.
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Cochlear Implant Outcomes and Genetic Mutations in Children with Ear and Brain Anomalies.
Busi M, Rosignoli M, Castiglione A, Minazzi F, Trevisi P, Aimoni C, Calzolari F, Granieri E, Martini A.
Busi M, et al.
Biomed Res Int. 2015;2015:696281. doi: 10.1155/2015/696281. Epub 2015 Jul 5.
Biomed Res Int. 2015.
PMID: 26236732
Free PMC article.
Clinical Trial.
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Association of the 4 g/5 g polymorphism of plasminogen activator inhibitor-1 gene with sudden sensorineural hearing loss. A case control study.
Cho SH, Chen H, Kim IS, Yokose C, Kang J, Cho D, Cai C, Palma S, Busi M, Martini A, Yoo TJ.
Cho SH, et al. Among authors: busi m.
BMC Ear Nose Throat Disord. 2012 Jun 6;12:5. doi: 10.1186/1472-6815-12-5.
BMC Ear Nose Throat Disord. 2012.
PMID: 22672326
Free PMC article.
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The universal newborn hearing screening program at the University Hospital of Ferrara: focus on costs and software solutions.
Ciorba A, Hatzopoulos S, Busi M, Guerrini P, Petruccelli J, Martini A.
Ciorba A, et al. Among authors: busi m.
Int J Pediatr Otorhinolaryngol. 2008 Jun;72(6):807-16. doi: 10.1016/j.ijporl.2008.02.011. Epub 2008 Apr 18.
Int J Pediatr Otorhinolaryngol. 2008.
PMID: 18395270
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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: busi m.
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
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