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A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable trait.
- Published in:
- Human Genetics, 2007, v. 122, n. 1, p. 103, doi. 10.1007/s00439-007-0384-5
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- Article
SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct.
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- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0853-4
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- Article
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy.
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- Human Genetics, 2021, v. 140, n. 12, p. 1709, doi. 10.1007/s00439-021-02379-9
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- Article
Evolution of Class Ill Homeodomain-Leucine Zipper Genes in Streptophytes.
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- Genetics, 2006, v. 173, n. 1, p. 373, doi. 10.1534/genetics.105.054239
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- Article
Hearing Loss and Irritability Reporting Without Vestibular Differences in Explosive Breaching Professionals.
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- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.588377
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- Article
Audiologic and Otologic Clinical Manifestations of Loeys-Dietz Syndrome: A Heritable Connective Tissue Disorder.
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- Otolaryngology-Head & Neck Surgery, 2022, v. 166, n. 2, p. 357, doi. 10.1177/01945998211008899
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- Article
Optic neuropathy in McCune-Albright syndrome: effects of early diagnosis and treatment of growth hormone excess.
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- 2013
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- Publication type:
- journal article
Charles Wells & Erasmus Darwin: The Dueling 'Vertiginous Philosophers'.
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- Audiology Today, 2019, v. 3, n. 1, p. 46
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- Article
Association of Hearing Loss and Otologic Outcomes With Fibrous Dysplasia.
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- 2018
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- Publication type:
- journal article
Audiovestibular Findings in a Cohort of Patients with Chiari Malformation Type I and Dizziness.
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- Journal of Clinical Medicine, 2023, v. 12, n. 8, p. 2767, doi. 10.3390/jcm12082767
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- Article
Discrimination Task Reveals Differences in Neural Bases of Tinnitus and Hearing Impairment.
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- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0026639
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- Article
Tune Deafness: Processing Melodic Errors Outside of Conscious Awareness as Reflected by Components of the Auditory ERP.
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- PLoS ONE, 2008, v. 3, n. 6, p. 1, doi. 10.1371/journal.pone.0002349
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- Publication type:
- Article
Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI).
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- Orphanet Journal of Rare Diseases, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13023-022-02410-w
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- Publication type:
- Article
Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI).
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- 2022
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- Publication type:
- journal article
Otologic manifestations of Fanconi anemia and other inherited bone marrow failure syndromes.
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- 2016
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- Publication type:
- journal article
Phase 1 trial and pharmacokinetic study of the oral platinum analog satraplatin in children and young adults with refractory solid tumors including brain tumors.
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- Pediatric Blood & Cancer, 2015, v. 62, n. 4, p. 603, doi. 10.1002/pbc.25344
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- Publication type:
- Article
P4‐127: MEDICARE COVERAGE FOR HOME HEALTH AIDE SERVICES: ADVOCATING FOR POLICY CHANGE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1487, doi. 10.1016/j.jalz.2018.06.2531
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- Article
A SUPPORT GROUP FOR CAREGIVERS OF PERSONS DIAGNOSED WITH LEWY BODY DEMENTIA.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P789, doi. 10.1016/j.jalz.2016.06.1588
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- Article
The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literature.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 3, p. 618, doi. 10.1002/ajmg.c.31823
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- Article
Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degeneration.
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- 2013
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- Publication type:
- journal article
Auditory analysis of xeroderma pigmentosum 1971–2012: hearing function, sun sensitivity and DNA repair predict neurological degeneration.
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- Brain: A Journal of Neurology, 2013, v. 136, n. 1, p. 194, doi. 10.1093/brain/aws317
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- Article
Audiometric and Otologic Findings in Children and Young Adults with Neurofibromatosis Type 1 and Plexiform Neurofibromas.
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- Laryngoscope, 2023, v. 133, n. 10, p. 2770, doi. 10.1002/lary.30522
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- Publication type:
- Article
Evolution of the Class IV HD-Zip Gene Family in Streptophytes.
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- Molecular Biology & Evolution, 2013, v. 30, n. 10, p. 2347, doi. 10.1093/molbev/mst132
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- Publication type:
- Article
Chimeric Negative Regulation of p14ARF and TBX1 by a t(9;22) Translocation Associated with Melanoma, Deafness, and DNA Repair Deficiency.
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- Human Mutation, 2013, v. 34, n. 9, p. 1250, doi. 10.1002/humu.22354
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- Publication type:
- Article
Hypo-Functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms?
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- Human Mutation, 2009, v. 30, n. 4, p. 599, doi. 10.1002/humu.20884
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- Publication type:
- Article
SLC26A4 Genotypes and Phenotypes Associated with Enlargement of the Vestibular Aqueduct.
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- Cellular Physiology & Biochemistry (Karger AG), 2011, v. 28, n. 3, p. 545, doi. 10.1159/000335119
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- Article
Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4.
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- 2017
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- Publication type:
- journal article
Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.
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- 2016
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- Publication type:
- journal article
Surgical resection of endolymphatic sac tumors in von Hippel-Lindau disease: Findings, results, and indications.
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- Laryngoscope, 2013, v. 123, n. 2, p. 477, doi. 10.1002/lary.23646
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- Publication type:
- Article
Otologic and audiologic manifestations of hutchinson-gilford progeria syndrome.
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- Laryngoscope, 2011, v. 121, n. 10, p. 2250, doi. 10.1002/lary.22151
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- Publication type:
- Article
Audiologic and Otologic Manifestations of Hutchinson-Gilford Progeria Syndrome.
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- Laryngoscope, 2010, v. 120, n. S3, p. S71, doi. 10.1002/lary.21260
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- Article
SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct.
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- Laryngoscope, 2010, v. 120, n. 2, p. 384, doi. 10.1002/lary.20722
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- Publication type:
- Article
Use of SLC26A4 Mutation Testing for Unilateral Enlargement of the Vestibular Aqueduct.
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- JAMA Otolaryngology-Head & Neck Surgery, 2013, v. 139, n. 9, p. 907, doi. 10.1001/jamaoto.2013.4185
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- Publication type:
- Article
Auditory phenotype of Smith–Lemli–Opitz syndrome.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 4, p. 1131, doi. 10.1002/ajmg.a.62087
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- Article
Audiovestibular Characteristics of Small Cochleovestibular Schwannomas in Neurofibromatosis Type 2.
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- 2014
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- Publication type:
- journal article
Audiovestibular Characteristics of Small Cochleovestibular Schwannomas in Neurofibromatosis Type 2.
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- Otolaryngology-Head & Neck Surgery, 2013, v. 149, n. 2, p. P92, doi. 10.1177/0194599813495815a174
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- Article
Audiovestibular dysfunction associated with adoptive cell immunotherapy for melanoma.
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- 2012
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- Publication type:
- journal article
Audiovestibular Dysfunction Associated with Adoptive Cell Immunotherapy for Melanoma.
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- Otolaryngology-Head & Neck Surgery, 2012, v. 147, n. 4, p. 744, doi. 10.1177/0194599812448356
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- Article
Audiovestibular Dysfunction Associated with Adoptive Cell Therapy for Melanoma.
- Published in:
- 2011
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- Publication type:
- Abstract
Otologic Disease in Polyostotic Fibrous Dysplasia and McCune‐Albright Syndrome.
- Published in:
- 2011
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- Publication type:
- Abstract
Cryopyrin-Associated Periodic Syndromes: Otolaryngologic and Audiologic Manifestations.
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- Otolaryngology-Head & Neck Surgery, 2011, v. 145, n. 2, p. 295, doi. 10.1177/0194599811402296
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- Publication type:
- Article
Cryopyrin-Associated Periodic Syndromes: ENT Manifestations
- Published in:
- 2010
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- Publication type:
- Abstract
P129: Cochlear Implantation and Bilateral Endolymphatic Sac Tumors
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- 2006
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- Publication type:
- Abstract
P129: Cochlear Implantation and Bilateral Endolymphatic Sac Tumors.
- Published in:
- 2006
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- Publication type:
- Abstract
Otolaryngologic markers for early diagnosis of turner syndrome
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- 2004
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- Publication type:
- Abstract
Auditory Phenotype of Smith-Magenis Syndrome.
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- Journal of Speech, Language & Hearing Research, 2017, v. 60, n. 4, p. 1076, doi. 10.1044/2016_JSLHR-H-16-0024
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- Publication type:
- Article
Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 2, p. 226, doi. 10.1111/cge.13868
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- Publication type:
- Article