Year |
Citation |
Score |
2021 |
Mao D, Wunderlich J, Savkovic B, Jeffreys E, Nicholls N, Lee OW, Eager M, McKay CM. Speech token detection and discrimination in individual infants using functional near-infrared spectroscopy. Scientific Reports. 11: 24006. PMID 34907273 DOI: 10.1038/s41598-021-03595-z |
0.313 |
|
2006 |
Wunderlich JL, Cone-Wesson BK. Maturation of CAEP in infants and children: a review. Hearing Research. 212: 212-23. PMID 16480841 DOI: 10.1016/J.Heares.2005.11.008 |
0.425 |
|
2006 |
Wunderlich JL, Cone-Wesson BK, Shepherd R. Maturation of the cortical auditory evoked potential in infants and young children. Hearing Research. 212: 185-202. PMID 16459037 DOI: 10.1016/J.Heares.2005.11.010 |
0.513 |
|
2003 |
Cone-Wesson B, Wunderlich J. Auditory evoked potentials from the cortex: audiology applications. Current Opinion in Otolaryngology & Head and Neck Surgery. 11: 372-7. PMID 14502069 DOI: 10.1097/00020840-200310000-00011 |
0.499 |
|
2002 |
Rance G, Cone-Wesson B, Wunderlich J, Dowell R. Speech perception and cortical event related potentials in children with auditory neuropathy. Ear and Hearing. 23: 239-53. PMID 12072616 DOI: 10.1097/00003446-200206000-00008 |
0.49 |
|
2001 |
Dahl HH, Saunders K, Kelly TM, Osborn AH, Wilcox S, Cone-Wesson B, Wunderlich JL, Du Sart D, Kamarinos M, Gardner RJ, Dennehy S, Williamson R, Vallance N, Mutton P. Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness. The Medical Journal of Australia. 175: 191-4. PMID 11587277 DOI: 10.5694/J.1326-5377.2004.Tb06368.X |
0.365 |
|
2001 |
Wunderlich JL, Cone-Wesson BK. Effects of stimulus frequency and complexity on the mismatch negativity and other components of the cortical auditory-evoked potential. The Journal of the Acoustical Society of America. 109: 1526-37. PMID 11325124 DOI: 10.1121/1.1349184 |
0.448 |
|
2000 |
Wilcox SA, Saunders K, Osborn AH, Arnold A, Wunderlich J, Kelly T, Collins V, Wilcox LJ, McKinlay Gardner RJ, Kamarinos M, Cone-Wesson B, Williamson R, Dahl HH. High frequency hearing loss correlated with mutations in the GJB2 gene. Human Genetics. 106: 399-405. PMID 10830906 DOI: 10.1007/S004390000273 |
0.41 |
|
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