Genetic Characteristics and Audiological Performance After Cochlear Implantation in Patients With Incomplete Partition Type III

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참고문헌 (19)

1. Sennaroglu L, "Surgical results of cochlear implantation in malformed cochlea", Otol Neurotol, 27(5), pp.615~623 (2006)
2. Nance WE, "X-linked mixed deafness with congenital fixation of the stapedial footplate and perilymphatic gusher", Birth Defects Orig Artic Ser, 7(4), pp.64~69 (1971)
3. Corvino V, "X-linked sensorineural hearing loss : a literature review", Curr Genomics, 19(5), pp.327~338 (2018)
4. Bademci G, "Novel domain-specific POU3F4 mutations are associated with X-linked deafness : examples from different populations", BMC Med Genet, 16, pp.9~ (2015)
5. de Kok YJ, "Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4", Science, 267(5198), pp.685~688 (1995)
6. 배성훈, "Cochlear Implants for Patients With Common Cavity Deformities and the Impact of Electrode Positioning", Clinical and Experimental Otorhinolaryngology, 15(1), pp.77~83 (2022), 대한이비인후과학회[DOI]
7. Sennaroglu L, "Incomplete partition type III : a rare and difficult cochlear implant surgical indication", Auris Nasus Larynx, 45(1), pp.26~32 (2018)
8. Sun J, "Outcomes of cochlear implantation in patients with incomplete partition type III", Int J Pediatr Otorhinolaryngol, 131, pp.109890~ (2020)
9. Chao X, "Cochlear implantation in a patient with a novel POU3F4 mutation and incomplete partition type-III malformation", Neural Plast, 2020, pp.8829587~ (2020)
10. Alballaa A, "Incomplete partition type III revisited-long-term results following cochlear implant", HNO, 68(Suppl 1), pp.25~32 (2020)
11. Jung J, "Cleaved cochlin sequesters pseudomonas aeruginosa and activates innate immunity in the inner ear", Cell Host Microbe, 25(4), pp.513~525 (2019)[DOI]
12. Jung J, "Genetic predisposition to sporadic congenital hearing loss in a pediatric population", Sci Rep, 7, pp.45973~ (2017)
13. Rim JH, "Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation", Hum Genet, 141(3-4), pp.915~927 (2022)
14. Friedman RA, "Molecular analysis of the POU3F4 gene in patients with clinical and radiographic evidence of X-linked mixed deafness with perilymphatic gusher", Ann Otol Rhinol Laryngol, 106(4), pp.320~325 (1997)
15. 반명진, "불완전 분할 3형 내이기형 환자에서 시행한 인공와우 이식술 1예", 대한이비인후-두경부외과학회지, 56(9), pp.594~598 (2013), 대한이비인후과학회[DOI]
16. Lee HK, "Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein", Physiol Genomics, 39(3), pp.195~201 (2009)
17. Song MH, "Clinical evaluation of DFN3 patients with deletions in the POU3F4 locus and detection of carrier female using MLPA", Clin Genet, 78(6), pp.524~532 (2010)
18. Jo HD, "Genetic load of alternations of transcription factor genes in non-syndromic deafness and the associated clinical phenotypes : experience from two tertiary referral centers", Biomedicines, 10(9), pp.2125~ (2022)
19. Choi BY, "Clinical observations and molecular variables of patients with hearing loss and incomplete partition type III", Laryngoscope, 126(3), pp.E123~8 (2016)

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