Results 71 to 80 of about 258,829 (315)
HAP1 interaction with KCNQ4 attenuates channel surface expression and function
Molecules and Cells: The voltage–gated channel subfamily Q member 4 (KCNQ4), a K+ channel, is one of the most frequently mutated genes in autosomal dominant nonsyndromic hearing loss.
Jung Ah Kim +6 more
doaj +1 more source
Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation
Neural Plasticity, 2020 Hereditary hearing loss is characterized by remarkable phenotypic heterogeneity. Patients with the same pathogenic mutations may exhibit various hearing loss phenotypes.
Chang Guo +9 more
doaj +1 more source
Arthritis Care &Research, EarlyView.People with systemic autoimmune and rheumatic diseases (SARDs) are at higher risk than the general population of experiencing adverse pregnancy and perinatal outcomes such as preeclampsia, intrauterine growth restriction, and maternal and/or fetal death.
Mehret Birru Talabi, Sonya Borrero
wiley +1 more source
Examples of the journey through hearing loss [PDF]
, 2017 Hearing loss is a common chronic condition which is often poorly recognized but can have multiple negative impacts, not just on the lives of those directly affected, but also those living with them.
Gullacksen, Ann-Christine
core
Word Recognition and Learning: Effects of Hearing Loss and Amplification Feature [PDF]
, 2017 : Two amplification features were examined using auditory tasks that varied in stimulus familiarity. It was expected that the benefits of certain amplification features would increase as the familiarity with the stimuli decreased.
core +1 more source
Development of a Disease Activity Index for the Assessment of VEXAS Syndrome (VEXAS‐DAI)
Arthritis Care &Research, Accepted Article.Objective VEXAS syndrome is characterized by a complex spectrum of inflammatory and hematologic manifestations. Clinical research to identify effective therapies is urgently needed but is hindered by the lack of validated outcome measures. A VEXAS‐specific disease activity index (DAI) is an essential tool for reliably capturing changes in disease ...
Kevin Byram +25 more
wiley +1 more source
Scientific ReportsHearing loss is genetically heterogeneous, with over 121 implicated genes. Minor allele frequency (MAF) data from population databases greatly aid variant interpretation; however, these databases are predominantly based on individuals of European ...
Sun Young Joo +6 more
doaj +1 more source
Brazilian Journal of OtorhinolaryngologyAccording to the World Health Organization, significant hearing loss in young people exposed to recreational acoustic trauma has become a public health issue.
Lara Freire Bezerril Soares +7 more
doaj +1 more source
Outcomes of unilateral idiopathic sudden sensorineural hearing loss: Two decades of experience
Laryngoscope Investigative Otolaryngology, 2019 Objectives (a) Determine the demographic and medical risk factors for patients who presented with unilateral idiopathic sudden sensorineural hearing loss (ISSNHL); (b) identify treatments that patients underwent; (c) evaluate the adequacy of follow‐up ...
Yanjun Xie +3 more
doaj +1 more source
Rheumatology and Immunology Research, 2021 Huang, Wenhan, Wang, Yi, Shen, Min
openaire +2 more sources