Pandya A - 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: pandya a. 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: pandya a. 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

Risk factors associated with unilateral hearing loss.

Yelverton JC, Dominguez LM, Chapman DA, Wang S, Pandya A, Dodson KM. Yelverton JC, et al. Among authors: pandya a. JAMA Otolaryngol Head Neck Surg. 2013 Jan;139(1):59-63. doi: 10.1001/jamaoto.2013.1097. JAMA Otolaryngol Head Neck Surg. 2013. PMID: 23329092

4

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

Yelverton JC, Dodson KM, Arnos K, Pandya A. Yelverton JC, et al. Among authors: pandya a. Otolaryngol Head Neck Surg. 2013 Nov;149(5):795-6. doi: 10.1177/0194599813502927. Otolaryngol Head Neck Surg. 2013. PMID: 24190891 No abstract available.

5

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: pandya a. Hum Mol Genet. 2003 May 15;12(10):1155-62. doi: 10.1093/hmg/ddg127. Hum Mol Genet. 2003. PMID: 12719379

6

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. Genet Med. 2003 Jul-Aug;5(4):295-303. doi: 10.1097/01.GIM.0000078026.01140.68. Genet Med. 2003. PMID: 12865758

7

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: pandya a. Ear Hear. 2005 Jun;26(3):361-9. doi: 10.1097/00003446-200506000-00011. Ear Hear. 2005. PMID: 15937416

8

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: pandya a. Ear Hear. 2006 Dec;27(6):732-41. doi: 10.1097/01.aud.0000240492.78561.d3. Ear Hear. 2006. PMID: 17086082

9

Consumer motivations for pursuing genetic testing and their preferences for the provision of genetic services for hearing loss.

Withrow KA, Burton S, Arnos KS, Kalfoglou A, Pandya A. Withrow KA, et al. Among authors: pandya a. J Genet Couns. 2008 Jun;17(3):252-60. doi: 10.1007/s10897-007-9143-y. Epub 2008 Feb 5. J Genet Couns. 2008. PMID: 18247107

10

Impact of genetic advances and testing for hearing loss: results from a national consumer survey.

Withrow KA, Tracy KA, Burton SK, Norris VW, Maes HH, Arnos KS, Pandya A. Withrow KA, et al. Among authors: pandya a. Am J Med Genet A. 2009 Jun;149A(6):1159-68. doi: 10.1002/ajmg.a.32800. Am J Med Genet A. 2009. PMID: 19449400

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