Aging of the human vestibular system
CK Zalewski - Seminars in hearing, 2015 - thieme-connect.com
Aging affects every sensory system in the body, including the vestibular system. Although its
impact is often difficult to quantify, the deleterious impact of aging on the vestibular system is …
impact is often difficult to quantify, the deleterious impact of aging on the vestibular system is …
SLC26A4 Genotypes and Phenotypes Associated with Enlargement of the Vestibular Aqueduct
T Ito, BY Choi, KA King, CK Zalewski… - Cellular Physiology and …, 2011 - karger.com
Enlargement of the vestibular aqueduct (EVA) is the most common inner ear anomaly
detected in ears of children with sensorineural hearing loss. Pendred syndrome (PS) is an …
detected in ears of children with sensorineural hearing loss. Pendred syndrome (PS) is an …
Inhaled amikacin for treatment of refractory pulmonary nontuberculous mycobacterial disease
KN Olivier, PA Shaw, TS Glaser… - Annals of the …, 2014 - atsjournals.org
Rationale: Treatment of pulmonary nontuberculous mycobacteria, especially Mycobacterium
abscessus, requires prolonged, multidrug regimens with high toxicity and suboptimal …
abscessus, requires prolonged, multidrug regimens with high toxicity and suboptimal …
Atypical and ultra-rare Usher syndrome: a review
RM Nolen, RB Hufnagel, TB Friedman… - Ophthalmic …, 2020 - Taylor & Francis
Usher syndrome has classically been described as a combination of hearing loss and rod-
cone dystrophy; vestibular dysfunction is present in many patients. Three distinct clinical …
cone dystrophy; vestibular dysfunction is present in many patients. Three distinct clinical …
Hypo‐Functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype‐phenotype correlation or …
BY Choi, AK Stewart, AC Madeo, SP Pryor… - Human …, 2009 - Wiley Online Library
Hearing loss with enlargement of the vestibular aqueduct (EVA) can be associated with
mutations of the SLC26A4 gene encoding pendrin, a transmembrane Cl−/I−/HCO …
mutations of the SLC26A4 gene encoding pendrin, a transmembrane Cl−/I−/HCO …
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes
JM Schultz, R Bhatti, AC Madeo, A Turriff… - Journal of medical …, 2011 - jmg.bmj.com
Background Recessive mutant alleles of MYO7A, USH1C, CDH23, and PCDH15 cause non-
syndromic deafness or type 1 Usher syndrome (USH1) characterised by deafness …
syndromic deafness or type 1 Usher syndrome (USH1) characterised by deafness …
Optic neuropathy in McCune-Albright syndrome: effects of early diagnosis and treatment of growth hormone excess
AM Boyce, MK Glover, MH Kelly… - The Journal of …, 2013 - academic.oup.com
Context: GH excess is a serious complication of McCune-Albright syndrome (MAS) and has
been associated with craniofacial morbidity. Objective: The aim of the study was to …
been associated with craniofacial morbidity. Objective: The aim of the study was to …
Association of hearing loss and otologic outcomes with fibrous dysplasia
Importance Fibrous dysplasia (FD) and McCune-Albright syndrome (MAS) are rare bone
and endocrine disorders in which expansile fibro-osseous lesions result in deformity, pain …
and endocrine disorders in which expansile fibro-osseous lesions result in deformity, pain …
Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes
BY Choi, AC Madeo, KA King, CK Zalewski… - Journal of medical …, 2009 - jmg.bmj.com
Background: Hearing loss with enlarged vestibular aqueduct (EVA) can be inherited as an
autosomal recessive trait caused by bi-allelic mutations of SLC26A4. However, many EVA …
autosomal recessive trait caused by bi-allelic mutations of SLC26A4. However, many EVA …
Analysis of auditory phenotype and karyotype in 200 females with Turner syndrome
KA King, T Makishima, CK Zalewski, VK Bakalov… - Ear and …, 2007 - journals.lww.com
Objectives: Turner syndrome is the most common sex chromosome disorder in females, and
is caused by a total or partial deletion of one X chromosome. The purpose of this study was …
is caused by a total or partial deletion of one X chromosome. The purpose of this study was …