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Page 1
The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.
Ealy M, Lynch KA, Meyer NC, Smith RJ. Ealy M, et al. Laryngoscope. 2011 Jun;121(6):1184-6. doi: 10.1002/lary.21778. Epub 2011 Apr 14. Laryngoscope. 2011. PMID: 21495045
Commentary on "Otosclerosis: thirty-year follow-up after surgery".
Ealy M, Schrauwen I, Van Camp G. Ealy M, et al. Ann Otol Rhinol Laryngol. 2011 Sep;120(9):615-6. doi: 10.1177/000348941112000910. Ann Otol Rhinol Laryngol. 2011. PMID: 22032076 No abstract available.
The genetics of otosclerosis.
Ealy M, Smith RJ. Ealy M, et al. Hear Res. 2010 Jul;266(1-2):70-4. doi: 10.1016/j.heares.2009.07.002. Epub 2009 Jul 14. Hear Res. 2010. PMID: 19607896 Review.
Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder.
Zong L, Guan J, Ealy M, Zhang Q, Wang D, Wang H, Zhao Y, Shen Z, Campbell CA, Wang F, Yang J, Sun W, Lan L, Ding D, Xie L, Qi Y, Lou X, Huang X, Shi Q, Chang S, Xiong W, Yin Z, Yu N, Zhao H, Wang J, Wang J, Salvi RJ, Petit C, Smith RJ, Wang Q. Zong L, et al. Among authors: ealy m. J Med Genet. 2015 Aug;52(8):523-31. doi: 10.1136/jmedgenet-2014-102961. Epub 2015 May 18. J Med Genet. 2015. PMID: 25986071 Free PMC article.
Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling.
Ealy M, Meyer NC, Corchado JC, Schrauwen I, Bress A, Pfister M, Van Camp G, Smith RJ. Ealy M, et al. Otol Neurotol. 2014 Mar;35(3):395-400. doi: 10.1097/MAO.0000000000000244. Otol Neurotol. 2014. PMID: 24492129 Free PMC article.
Otosclerosis.
Ealy M, Smith RJH. Ealy M, et al. Adv Otorhinolaryngol. 2011;70:122-129. doi: 10.1159/000322488. Epub 2011 Feb 24. Adv Otorhinolaryngol. 2011. PMID: 21358194 Review.
COL1A1 association and otosclerosis: a meta-analysis.
Schrauwen I, Khalfallah A, Ealy M, Fransen E, Claes C, Huber A, Murillo LR, Masmoudi S, Smith RJ, Van Camp G. Schrauwen I, et al. Among authors: ealy m. Am J Med Genet A. 2012 May;158A(5):1066-70. doi: 10.1002/ajmg.a.35276. Epub 2012 Apr 9. Am J Med Genet A. 2012. PMID: 22489040
Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia.
Khalfallah A, Schrauwen I, Mnaja M, Fransen E, Lahmar I, Ealy M, Dhouib L, Ayadi H, Charfedine I, Driss N, Ghorbel A, Smith RJ, Masmoudi S, Van Camp G. Khalfallah A, et al. Among authors: ealy m. Ann Hum Genet. 2010 Sep 1;74(5):399-405. doi: 10.1111/j.1469-1809.2010.00595.x. Epub 2010 Jul 14. Ann Hum Genet. 2010. PMID: 20642811
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.
Schrauwen I, Ealy M, Fransen E, Vanderstraeten K, Thys M, Meyer NC, Cosgarea M, Huber A, Mazzoli M, Pfister M, Smith RJ, Van Camp G. Schrauwen I, et al. Among authors: ealy m. Hum Genet. 2010 Feb;127(2):155-62. doi: 10.1007/s00439-009-0754-2. Epub 2009 Oct 22. Hum Genet. 2010. PMID: 19847460
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
Schrauwen I, Ealy M, Huentelman MJ, Thys M, Homer N, Vanderstraeten K, Fransen E, Corneveaux JJ, Craig DW, Claustres M, Cremers CW, Dhooge I, Van de Heyning P, Vincent R, Offeciers E, Smith RJ, Van Camp G. Schrauwen I, et al. Among authors: ealy m. Am J Hum Genet. 2009 Mar;84(3):328-38. doi: 10.1016/j.ajhg.2009.01.023. Epub 2009 Feb 19. Am J Hum Genet. 2009. PMID: 19230858 Free PMC article.
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