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Quoted phrase not found in phrase index: "Aplasia/Hypoplasia of the ear"
Page 1
Vestibular function in children with vestibulocochlear nerve aplasia/hypoplasia.
Karpeta N, Asp F, Edholm K, Bonnard Å, Wales J, Karltorp E, Duan M, Verrecchia L. Karpeta N, et al. Acta Otolaryngol. 2023 Oct;143(10):861-866. doi: 10.1080/00016489.2023.2285453. Epub 2024 Jan 5. Acta Otolaryngol. 2023. PMID: 38063358

The presence of a normal response to any test doubled the likelihood of a measured hearing threshold after CI, the best predictors being the BCcVEMP and vHIT (p < 0.05). CONCLUSION: Canal function may represent a predictor of auditive pathway integrity with a pos

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The presence of a normal response to any test doubled the likelihood of a measured hearing threshold after CI, the best predictors be …
Cochlear Implant Outcomes in Cochlea Nerve Aplasia and Hypoplasia.
Birman CS, Powell HR, Gibson WP, Elliott EJ. Birman CS, et al. Otol Neurotol. 2016 Jun;37(5):438-45. doi: 10.1097/MAO.0000000000000997. Otol Neurotol. 2016. PMID: 27050647
OBJECTIVE: To assess cochlear implant (CI) outcomes, and factors affecting outcomes, for children with aplasia/ hypoplasia of the cochlea nerve. We also developed a new grading system for the nerves of the internal auditory meatus (IAM) and cochlea nerve classificat …
OBJECTIVE: To assess cochlear implant (CI) outcomes, and factors affecting outcomes, for children with aplasia/ hypoplasia of …
Radiological Imaging Findings of Patients with Congenital Totally Hearing Loss.
Dağkıran M, Dağkıran N, Sürmelioğlu Ö, Ballı T, Tuncer Ü, Akgül E, Çetik F. Dağkıran M, et al. J Int Adv Otol. 2016 Apr;12(1):43-8. doi: 10.5152/iao.2015.1450. J Int Adv Otol. 2016. PMID: 27340982 Free article.
Dilatation of the internal acoustic canal was found in 42 ears (30.9%); also, 21 ears with cochlear nerve aplasia/hypoplasia (15.4%), 5 ears with internal acoustic canal aplasia, and 1 ear with internal acoustic canal hypoplasia (0.73%) were detected. There w …
Dilatation of the internal acoustic canal was found in 42 ears (30.9%); also, 21 ears with cochlear nerve aplasia/hypoplasia ( …
Etiology and therapy indication for cochlear implantation in children with single-sided deafness : Retrospective analysis.
Cushing SL, Gordon KA, Sokolov M, Papaioannou V, Polonenko M, Papsin BC. Cushing SL, et al. HNO. 2019 Oct;67(10):750-759. doi: 10.1007/s00106-019-00729-8. HNO. 2019. PMID: 31478064 English.
More than half of children did not go on to implantation (63/103, 61%), with the 2 main reasons being (1) half (31/63) did not meet candidacy criteria for implantation, most commonly due to cochlear nerve aplasia/hypoplasia (31/82 who were assessed with MRI, 38%) an …
More than half of children did not go on to implantation (63/103, 61%), with the 2 main reasons being (1) half (31/63) did not meet candidac …
Bimodal stimulation in children with inner ear malformation: One side cochlear implant and contralateral auditory brainstem implant.
Batuk MO, Cinar BC, Yarali M, Aslan F, Ozkan HB, Sennaroglu G, Yucel E, Bajin MD, Bilginer B, Sennaroglu L. Batuk MO, et al. Clin Otolaryngol. 2020 Mar;45(2):231-238. doi: 10.1111/coa.13499. Epub 2020 Jan 22. Clin Otolaryngol. 2020. PMID: 31854074
OBJECTIVE: To determine audiological outcomes of children who use a cochlear implant (CI) in one ear and an auditory brainstem implant (ABI) in the contralateral ear. ...PARTICIPANTS: Twelve children followed with CI and contralateral auditory brainstem implant (ABI …
OBJECTIVE: To determine audiological outcomes of children who use a cochlear implant (CI) in one ear and an auditory brainstem implan …
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis.
de Munnik SA, Bicknell LS, Aftimos S, Al-Aama JY, van Bever Y, Bober MB, Clayton-Smith J, Edrees AY, Feingold M, Fryer A, van Hagen JM, Hennekam RC, Jansweijer MC, Johnson D, Kant SG, Opitz JM, Ramadevi AR, Reardon W, Ross A, Sarda P, Schrander-Stumpel CT, Schoots J, Temple IK, Terhal PA, Toutain A, Wise CA, Wright M, Skidmore DL, Samuels ME, Hoefsloot LH, Knoers NV, Brunner HG, Jackson AP, Bongers EM. de Munnik SA, et al. Eur J Hum Genet. 2012 Jun;20(6):598-606. doi: 10.1038/ejhg.2011.269. Epub 2012 Feb 15. Eur J Hum Genet. 2012. PMID: 22333897 Free PMC article.
Meier-Gorlin syndrome (MGS) is an autosomal recessive disorder characterized by microtia, patellar aplasia/hypoplasia, and short stature. Recently, mutations in five genes from the pre-replication complex (ORC1, ORC4, ORC6, CDT1, and CDC6), crucial in cell-cycle pro …
Meier-Gorlin syndrome (MGS) is an autosomal recessive disorder characterized by microtia, patellar aplasia/hypoplasia, and sho …