Friedman RA - Search Results

1

Genetics of hearing loss: Allelism and modifier genes produce a phenotypic continuum.

McHugh RK, Friedman RA. McHugh RK, et al. Among authors: friedman ra. Anat Rec A Discov Mol Cell Evol Biol. 2006 Apr;288(4):370-81. doi: 10.1002/ar.a.20297. Anat Rec A Discov Mol Cell Evol Biol. 2006. PMID: 16550584 Free article. Review.

2

Nonsyndromic hereditary hearing loss.

Li XC, Friedman RA. Li XC, et al. Among authors: friedman ra. Otolaryngol Clin North Am. 2002 Apr;35(2):275-85. doi: 10.1016/s0030-6665(02)00013-0. Otolaryngol Clin North Am. 2002. PMID: 12391618 Review.

3

Genome-wide screening for genetic loci associated with noise-induced hearing loss.

White CH, Ohmen JD, Sheth S, Zebboudj AF, McHugh RK, Hoffman LF, Lusis AJ, Davis RC, Friedman RA. White CH, et al. Among authors: friedman ra. Mamm Genome. 2009 Apr;20(4):207-13. doi: 10.1007/s00335-009-9178-5. Epub 2009 Apr 1. Mamm Genome. 2009. PMID: 19337678 Free PMC article.

4

Large-scale phenotyping of noise-induced hearing loss in 100 strains of mice.

Myint A, White CH, Ohmen JD, Li X, Wang J, Lavinsky J, Salehi P, Crow AL, Ohyama T, Friedman RA. Myint A, et al. Among authors: friedman ra. Hear Res. 2016 Feb;332:113-120. doi: 10.1016/j.heares.2015.12.006. Epub 2015 Dec 17. Hear Res. 2016. PMID: 26706709 Free PMC article.

5

Maternally inherited nonsyndromic hearing loss.

Friedman RA, Bykhovskaya Y, Sue CM, DiMauro S, Bradley R, Fallis-Cunningham R, Paradies N, Pensak ML, Smith RJ, Groden J, Li XC, Fischel-Ghodsian N. Friedman RA, et al. Am J Med Genet. 1999 Jun 4;84(4):369-72. doi: 10.1002/(sici)1096-8628(19990604)84:4<369::aid-ajmg12>3.0.co;2-v. Am J Med Genet. 1999. PMID: 10340654

6

Profound hearing loss associated with hydrocodone/acetaminophen abuse.

Friedman RA, House JW, Luxford WM, Gherini S, Mills D. Friedman RA, et al. Am J Otol. 2000 Mar;21(2):188-91. doi: 10.1016/s0196-0709(00)80007-1. Am J Otol. 2000. PMID: 10733182

7

Intratympanic steroid injection for treatment of idiopathic sudden hearing loss.

Slattery WH, Fisher LM, Iqbal Z, Friedman RA, Liu N. Slattery WH, et al. Among authors: friedman ra. Otolaryngol Head Neck Surg. 2005 Aug;133(2):251-9. doi: 10.1016/j.otohns.2005.05.015. Otolaryngol Head Neck Surg. 2005. PMID: 16087024 Clinical Trial.

8

Identification of two major loci that suppress hearing loss and cochlear dysmorphogenesis in Eya1bor/bor mice.

Niu H, Makmura L, Shen T, Sheth SS, Blair K, Friedman RA. Niu H, et al. Among authors: friedman ra. Genomics. 2006 Sep;88(3):302-8. doi: 10.1016/j.ygeno.2006.01.005. Epub 2006 Feb 20. Genomics. 2006. PMID: 16488112 Free article.

9

Correction of progressive hearing loss in superior canal dehiscence syndrome.

Wilkinson EP, Liu GC, Friedman RA. Wilkinson EP, et al. Among authors: friedman ra. Laryngoscope. 2008 Jan;118(1):10-3. doi: 10.1097/MLG.0b013e31814b8d67. Laryngoscope. 2008. PMID: 18090259

10

Mapping of genetic modifiers of Eya1 ( bor/bor ) in CAST/EiJ and BALB/cJ that suppress cochlear aplasia and associated deafness.

Niu H, Li X, Makmura L, Friedman RA. Niu H, et al. Among authors: friedman ra. Mamm Genome. 2008 Sep;19(9):634-9. doi: 10.1007/s00335-008-9145-6. Epub 2008 Oct 4. Mamm Genome. 2008. PMID: 18836772

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