Brewer CC - Search Results

1

Atypical and ultra-rare Usher syndrome: a review.

Nolen RM, Hufnagel RB, Friedman TB, Turriff AE, Brewer CC, Zalewski CK, King KA, Wafa TT, Griffith AJ, Brooks BP, Zein WM. Nolen RM, et al. Among authors: brewer cc. Ophthalmic Genet. 2020 Oct;41(5):401-412. doi: 10.1080/13816810.2020.1747090. Epub 2020 May 6. Ophthalmic Genet. 2020. PMID: 32372680 Free PMC article. Review.

2

Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III.

Ness SL, Ben-Yosef T, Bar-Lev A, Madeo AC, Brewer CC, Avraham KB, Kornreich R, Desnick RJ, Willner JP, Friedman TB, Griffith AJ. Ness SL, et al. Among authors: brewer cc. J Med Genet. 2003 Oct;40(10):767-72. doi: 10.1136/jmg.40.10.767. J Med Genet. 2003. PMID: 14569126 Free PMC article. No abstract available.

3

Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.

Makishima T, Kurima K, Brewer CC, Griffith AJ. Makishima T, et al. Among authors: brewer cc. Otol Neurotol. 2004 Sep;25(5):714-9. doi: 10.1097/00129492-200409000-00011. Otol Neurotol. 2004. PMID: 15354000

4

SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.

Pryor SP, Madeo AC, Reynolds JC, Sarlis NJ, Arnos KS, Nance WE, Yang Y, Zalewski CK, Brewer CC, Butman JA, Griffith AJ. Pryor SP, et al. Among authors: brewer cc. J Med Genet. 2005 Feb;42(2):159-65. doi: 10.1136/jmg.2004.024208. J Med Genet. 2005. PMID: 15689455 Free PMC article. No abstract available.

5

Tumors of the endolymphatic sac in patients with von Hippel-Lindau disease: implications for their natural history, diagnosis, and treatment.

Kim HJ, Butman JA, Brewer C, Zalewski C, Vortmeyer AO, Glenn G, Oldfield EH, Lonser RR. Kim HJ, et al. J Neurosurg. 2005 Mar;102(3):503-12. doi: 10.3171/jns.2005.102.3.0503. J Neurosurg. 2005. PMID: 15796386

6

Investigation of the role of congenital cytomegalovirus infection in the etiology of enlarged vestibular aqueducts.

Pryor SP, Demmler GJ, Madeo AC, Yang Y, Zalewski CK, Brewer CC, Butman JA, Fowler KB, Griffith AJ. Pryor SP, et al. Among authors: brewer cc. Arch Otolaryngol Head Neck Surg. 2005 May;131(5):388-92. doi: 10.1001/archotol.131.5.388. Arch Otolaryngol Head Neck Surg. 2005. PMID: 15897416

7

Neuropathic and cerebrovascular correlates of hearing loss in Fabry disease.

Ries M, Kim HJ, Zalewski CK, Mastroianni MA, Moore DF, Brady RO, Dambrosia JM, Schiffmann R, Brewer CC. Ries M, et al. Among authors: brewer cc. Brain. 2007 Jan;130(Pt 1):143-50. doi: 10.1093/brain/awl310. Epub 2006 Nov 14. Brain. 2007. PMID: 17105746 Free PMC article.

8

Cochlear implantation for hearing loss associated with bilateral endolymphatic sac tumors in von Hippel-Lindau disease.

Jagannathan J, Lonser RR, Stanger RA, Butman JA, Vortmeyer AO, Zalewski CK, Brewer C, Surowicz C, Kim HJ. Jagannathan J, et al. Otol Neurotol. 2007 Oct;28(7):927-30. doi: 10.1097/MAO.0b013e31805c7506. Otol Neurotol. 2007. PMID: 17468670

9

A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable trait.

Morell RJ, Brewer CC, Ge D, Snieder H, Zalewski CK, King KA, Drayna D, Friedman TB. Morell RJ, et al. Among authors: brewer cc. Hum Genet. 2007 Aug;122(1):103-11. doi: 10.1007/s00439-007-0384-5. Epub 2007 May 29. Hum Genet. 2007. PMID: 17533509

10

Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.

Makishima T, Madeo AC, Brewer CC, Zalewski CK, Butman JA, Sachdev V, Arai AE, Holbrook BM, Rosing DR, Griffith AJ. Makishima T, et al. Among authors: brewer cc. Am J Med Genet A. 2007 Jul 15;143A(14):1592-8. doi: 10.1002/ajmg.a.31793. Am J Med Genet A. 2007. PMID: 17567890

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