Nance WE - Search Results

1

The clinical and audiologic features of hearing loss due to mitochondrial mutations.

Yelverton JC, Arnos K, Xia XJ, Nance WE, Pandya A, Dodson KM. Yelverton JC, et al. Among authors: nance we. Otolaryngol Head Neck Surg. 2013 Jun;148(6):1017-22. doi: 10.1177/0194599813482705. Epub 2013 Mar 22. Otolaryngol Head Neck Surg. 2013. PMID: 23525847

2

Etiology of unilateral hearing loss in a national hereditary deafness repository.

Dodson KM, Georgolios A, Barr N, Nguyen B, Sismanis A, Arnos KS, Norris VW, Chapman D, Nance WE, Pandya A. Dodson KM, et al. Among authors: nance we. Am J Otolaryngol. 2012 Sep-Oct;33(5):590-4. doi: 10.1016/j.amjoto.2012.03.005. Epub 2012 Apr 24. Am J Otolaryngol. 2012. PMID: 22534022

3

Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss.

Nance WE, Lim BG, Dodson KM. Nance WE, et al. J Clin Virol. 2006 Feb;35(2):221-5. doi: 10.1016/j.jcv.2005.09.017. Epub 2005 Dec 27. J Clin Virol. 2006. PMID: 16384744

4

Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.

Liu XZ, Ouyang XM, Xia XJ, Zheng J, Pandya A, Li F, Du LL, Welch KO, Petit C, Smith RJ, Webb BT, Yan D, Arnos KS, Corey D, Dallos P, Nance WE, Chen ZY. Liu XZ, et al. Among authors: nance we. Hum Mol Genet. 2003 May 15;12(10):1155-62. doi: 10.1093/hmg/ddg127. Hum Mol Genet. 2003. PMID: 12719379

5

Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.

Pandya A, Arnos KS, Xia XJ, Welch KO, Blanton SH, Friedman TB, Garcia Sanchez G, Liu MD XZ, Morell R, Nance WE. Pandya A, et al. Among authors: nance we. Genet Med. 2003 Jul-Aug;5(4):295-303. doi: 10.1097/01.GIM.0000078026.01140.68. Genet Med. 2003. PMID: 12865758

6

Audiological features of GJB2 (connexin 26) deafness.

Liu XZ, Pandya A, Angeli S, Telischi FF, Arnos KS, Nance WE, Balkany T. Liu XZ, et al. Among authors: nance we. Ear Hear. 2005 Jun;26(3):361-9. doi: 10.1097/00003446-200506000-00011. Ear Hear. 2005. PMID: 15937416

7

Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.

Norris VW, Arnos KS, Hanks WD, Xia X, Nance WE, Pandya A. Norris VW, et al. Among authors: nance we. Ear Hear. 2006 Dec;27(6):732-41. doi: 10.1097/01.aud.0000240492.78561.d3. Ear Hear. 2006. PMID: 17086082

8

Vestibular dysfunction in DFNB1 deafness.

Dodson KM, Blanton SH, Welch KO, Norris VW, Nuzzo RL, Wegelin JA, Marin RS, Nance WE, Pandya A, Arnos KS. Dodson KM, et al. Among authors: nance we. Am J Med Genet A. 2011 May;155A(5):993-1000. doi: 10.1002/ajmg.a.33828. Epub 2011 Apr 4. Am J Med Genet A. 2011. PMID: 21465647 Free PMC article.

9

Superficial siderosis: a potentially important cause of genetic as well as non-genetic deafness.

Dodson KM, Sismanis A, Nance WE. Dodson KM, et al. Among authors: nance we. Am J Med Genet A. 2004 Sep 15;130A(1):22-5. doi: 10.1002/ajmg.a.30050. Am J Med Genet A. 2004. PMID: 15368490

10

Familial unilateral deafness and delayed endolymphatic hydrops.

Dodson KM, Kamei T, Sismanis A, Nance WE. Dodson KM, et al. Among authors: nance we. Am J Med Genet A. 2007 Jul 15;143A(14):1661-5. doi: 10.1002/ajmg.a.31741. Am J Med Genet A. 2007. PMID: 17497713

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

254 results

Search Page