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Quoted phrase not found in phrase index: "Aplasia/Hypoplasia of the ear"
Page 1
The vestibulocochlear nerve: aplasia and hypoplasia in combination with inner ear malformations.
Giesemann AM, Kontorinis G, Jan Z, Lenarz T, Lanfermann H, Goetz F. Giesemann AM, et al. Eur Radiol. 2012 Mar;22(3):519-24. doi: 10.1007/s00330-011-2287-z. Epub 2011 Sep 30. Eur Radiol. 2012. PMID: 21960158
OBJECTIVE: To determine features of hypoplasia and aplasia of the vestibulocochlear nerve (VCN) in combination with inner ear malformations (IEMs). METHODS: Index cases were retrospectively selected from all IEMs collected since 1995. ...KEY POINTS: Vestibulocochlear nerve …
OBJECTIVE: To determine features of hypoplasia and aplasia of the vestibulocochlear nerve (VCN) in combination with inner ear malform …
Auditory brainstem implant candidacy in the United States in children 0-17 years old.
Kaplan AB, Kozin ED, Puram SV, Owoc MS, Shah PV, Hight AE, Sethi RKV, Remenschneider AK, Lee DJ. Kaplan AB, et al. Int J Pediatr Otorhinolaryngol. 2015 Mar;79(3):310-315. doi: 10.1016/j.ijporl.2014.11.023. Epub 2014 Dec 15. Int J Pediatr Otorhinolaryngol. 2015. PMID: 25577282 Free PMC article. Review.
Over the past decade, surgeons have begun implanting ABIs in pediatric patients who are unable to receive cochlear implants due to congenital or acquired malformations of the inner ear. No study has examined the potential population-level demand for ABIs in the United Stat …
Over the past decade, surgeons have begun implanting ABIs in pediatric patients who are unable to receive cochlear implants due to congenita …
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 …
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 …
Ratio of Vestibular Endolymph in Patients with Isolated Lateral Semicircular Canal Dysplasia.
Naganawa S, Kawai H, Sone M, Ikeda M. Naganawa S, et al. Magn Reson Med Sci. 2015;14(3):203-10. doi: 10.2463/mrms.2014-0112. Epub 2015 Mar 31. Magn Reson Med Sci. 2015. PMID: 25833266 Free article.
PURPOSE: Isolated vestibular-lateral semicircular canal dysplasia (LSCCD) is one of the most common anomalies of the inner ear. However, endolymphatic size in LSCCD is unknown. We measured the size of the endolymph in the vestibule of patients with LSCCD and compared it wi …
PURPOSE: Isolated vestibular-lateral semicircular canal dysplasia (LSCCD) is one of the most common anomalies of the inner ear. Howev …
Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorder.
de Munnik SA, Otten BJ, Schoots J, Bicknell LS, Aftimos S, Al-Aama JY, van Bever Y, Bober MB, Borm GF, Clayton-Smith J, Deal CL, 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, Sluiter AE, 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. Am J Med Genet A. 2012 Nov;158A(11):2733-42. doi: 10.1002/ajmg.a.35681. Epub 2012 Sep 28. Am J Med Genet A. 2012. PMID: 23023959
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterized by primordial dwarfism, microtia, and patellar aplasia/hypoplasia. Recently, mutations in the ORC1, ORC4, ORC6, CDT1, and CDC6 genes, encoding components of the pre-replication complex, …
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterized by primordial dwarfism, microtia, and patellar aplasia …
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 …