Publications by authors named "Carmen C Brewer"

57Publications

Stability of Early Auditory Evoked Potential Components Over Extended Test-Retest Intervals in Young Adults.

Ear Hear 2020 Nov/Dec;41(6):1461-1469

Audiology Unit, Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/AUD.0000000000000872DOI Listing
November 2020

Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndrome.

Clin Genet 2020 Oct 21. Epub 2020 Oct 21.

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/cge.13868DOI Listing
October 2020

Atypical and ultra-rare Usher syndrome: a review.

Ophthalmic Genet 2020 10 6;41(5):401-412. Epub 2020 May 6.

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/13816810.2020.1747090DOI Listing
October 2020

Stability of Early Auditory Evoked Potential Components Over Extended Test-Retest Intervals in Young Adults.

Ear Hear 2020 Apr 3. Epub 2020 Apr 3.

Audiology Unit, Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/AUD.0000000000000872DOI Listing
April 2020

Genetic Hearing Loss Associated With Autoinflammation.

Front Neurol 2020 5;11:141. Epub 2020 Mar 5.

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, United States.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3389/fneur.2020.00141DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066252PMC
March 2020

SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct.

BMC Med Genet 2019 07 2;20(1):118. Epub 2019 Jul 2.

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 35A Convent Drive, Room GF103, NIDCD/NIH, Bethesda, MD, USA.

View Article

Download full-text PDF

Source
https://bmcmedgenet.biomedcentral.com/articles/10.1186/s1288
Publisher Site
http://dx.doi.org/10.1186/s12881-019-0853-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604142PMC
July 2019

Audiologic and Otologic Complications of Cryptococcal Meningoencephalitis in Non-HIV Previously Healthy Patients.

Otol Neurotol 2019 07;40(6):e657-e664

Laboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/MAO.0000000000002242DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565454PMC
July 2019

All-night functional magnetic resonance imaging sleep studies.

J Neurosci Methods 2019 03 20;316:83-98. Epub 2018 Sep 20.

Advanced Magnetic Resonance Imaging Section, National Institute of Neurological Disorders and Stroke, USA; Section on Neuroadaptation and Protein Metabolism, National Institute of Mental Health, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jneumeth.2018.09.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524535PMC
March 2019

Examination of Utricular Response Using oVEMP and Unilateral Centrifugation Rotation Testing.

Ear Hear 2018 Sep/Oct;39(5):910-921

Audiology Unit, Otolaryngology Branch, National Institutes of Health (NIH), National Institute on Deafness and Other Communication Disorders (NIDCD), Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/AUD.0000000000000552DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425474PMC
March 2019

Clinical trials, ototoxicity grading scales and the audiologist's role in therapeutic decision making.

Int J Audiol 2018 09 23;57(sup4):S89-S98. Epub 2017 Dec 23.

a Audiology Unit, Otolaryngology Branch , National Institute on Deafness and Other Communication Disorders, National Institutes of Health , Bethesda , MD , USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/14992027.2017.1417644DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260812PMC
September 2018

Hearing Safety From Single- and Double-Pulse Transcranial Magnetic Stimulation in Children and Young Adults.

J Clin Neurophysiol 2017 Jul;34(4):340-347

*Human Motor Control Section, Medical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, U.S.A.; †Functional and Applied Biomechanics Lab, Rehabilitation Medicine Department, NIH Clinical Center, National Institutes of Health, Bethesda, Maryland, U.S.A.; ‡Biomedical Engineering, The Catholic University of America, Washington, District of Columbia, U.S.A.; and §Audiology Unit, Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, U.S.A.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/WNP.0000000000000372DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484061PMC
July 2017

Auditory Phenotype of Smith-Magenis Syndrome.

J Speech Lang Hear Res 2017 04;60(4):1076-1087

Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1044/2016_JSLHR-H-16-0024DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548078PMC
April 2017

Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4.

Laryngoscope 2017 07 15;127(7):E238-E243. Epub 2016 Nov 15.

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/lary.26418DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224160PMC
July 2017

Otologic manifestations of Fanconi anemia and other inherited bone marrow failure syndromes.

Pediatr Blood Cancer 2016 12 18;63(12):2139-2145. Epub 2016 Jul 18.

National Cancer Institute, National Institutes of Health, Rockville, Maryland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.26155DOI Listing
December 2016

Genetic causes of moderate to severe hearing loss point to modifiers.

Clin Genet 2017 Apr 6;91(4):589-598. Epub 2016 Oct 6.

Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, USA 20892.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/cge.12856DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365349PMC
April 2017

Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.

Laryngoscope 2016 07 20;126(7):E240-7. Epub 2015 Oct 20.

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/lary.25737DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838554PMC
July 2016

Vestibular Dysfunction in Patients with Enlarged Vestibular Aqueduct.

Otolaryngol Head Neck Surg 2015 Aug 12;153(2):257-62. Epub 2015 May 12.

National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health, Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/0194599815585098DOI Listing
August 2015

Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography.

Invest Ophthalmol Vis Sci 2014 Nov 25;56(1):107-14. Epub 2014 Nov 25.

National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1167/iovs.14-15355DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288141PMC
November 2014

Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type C.

J Assoc Res Otolaryngol 2014 Aug 17;15(4):529-41. Epub 2014 May 17.

National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, 20892, USA,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10162-014-0459-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141427PMC
August 2014

Audiovestibular Characteristics of Small Cochleovestibular Schwannomas in Neurofibromatosis Type 2.

Otolaryngol Head Neck Surg 2014 07 8;151(1):117-24. Epub 2014 Apr 8.

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/0194599814529081DOI Listing
July 2014

Auditory phenotype of Niemann-Pick disease, type C1.

Ear Hear 2014 Jan-Feb;35(1):110-7

1Department of Health and Human Services, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD; 2Department of Hearing and Speech Sciences, University of Maryland College Park, College Park, MD; 3Department of Health and Human Services, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD; 4Department of Human Development and Quantitative Methodology, University of Maryland College Park, College Park, MD.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/AUD.0b013e3182a362b8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895917PMC
August 2014

Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueduct.

JAMA Otolaryngol Head Neck Surg 2013 Sep;139(9):907-13

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jamaoto.2013.4185DOI Listing
September 2013

Systemic diagnostic testing in patients with apparently isolated uveal coloboma.

Am J Ophthalmol 2013 Dec 5;156(6):1159-1168.e4. Epub 2013 Sep 5.

Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajo.2013.06.037DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4167417PMC
December 2013

Histopathology of the inner ear in patients with xeroderma pigmentosum and neurologic degeneration.

Otol Neurotol 2013 Sep;34(7):1230-6

Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts 02114, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/MAO.0b013e31829795e9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3744623PMC
September 2013

mutation testing for hearing loss associated with enlargement of the vestibular aqueduct.

World J Otorhinolaryngol 2013 May;3(2):26-34

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, United States.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.5319/wjo.v3.i2.26DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423814PMC
May 2013

Optic neuropathy in McCune-Albright syndrome: effects of early diagnosis and treatment of growth hormone excess.

J Clin Endocrinol Metab 2013 Jan 23;98(1):E126-34. Epub 2012 Oct 23.

Skeletal Clinical Studies Unit, Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health (NIH), Bethesda, Maryland 20892, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1210/jc.2012-2111DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537097PMC
January 2013

Mechanisms of hearing loss in neurofibromatosis type 2.

PLoS One 2012 26;7(9):e46132. Epub 2012 Sep 26.

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0046132PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458837PMC
April 2013

Audiovestibular dysfunction associated with adoptive cell immunotherapy for melanoma.

Otolaryngol Head Neck Surg 2012 Oct 17;147(4):744-9. Epub 2012 May 17.

Department of Otolaryngology-Head and Neck Surgery, Georgetown University Medical Center, Washington, DC 20007, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/0194599812448356DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318787PMC
October 2012

SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueduct.

Cell Physiol Biochem 2011 18;28(3):545-52. Epub 2011 Nov 18.

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, Maryland 20850-3320, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000335119DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709178PMC
March 2012

Otolaryngologic markers for the early diagnosis of Turner syndrome.

Int J Pediatr Otorhinolaryngol 2009 Nov 3;73(11):1564-7. Epub 2009 Sep 3.

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20850-3320, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ijporl.2009.08.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2757481PMC
November 2009

Analysis of auditory phenotype and karyotype in 200 females with Turner syndrome.

Ear Hear 2007 Dec;28(6):831-41

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland 20892, USA.

View Article

Download full-text PDF

Source
http://turners.nichd.nih.gov/pdf/Hearong%20loss.pdf
Web Search
http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
Publisher Site
http://dx.doi.org/10.1097/AUD.0b013e318157677fDOI Listing
December 2007

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

Am J Med Genet A 2007 Jul;143A(14):1592-8

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville 20850-3320, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.31793DOI Listing
July 2007

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

Hum Genet 2007 Aug 29;122(1):103-11. Epub 2007 May 29.

Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA.

View Article

Download full-text PDF

Source
http://link.springer.com/10.1007/s00439-007-0384-5
Publisher Site
http://dx.doi.org/10.1007/s00439-007-0384-5DOI Listing
August 2007

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

Arch Otolaryngol Head Neck Surg 2005 May;131(5):388-92

Hearing Section, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archotol.131.5.388DOI Listing
May 2005

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

Otol Neurotol 2004 Sep;25(5):714-9

Section on Gene Structure and Function, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, Maryland 20850, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/00129492-200409000-00011DOI Listing
September 2004