Results 141 to 150 of about 55,611 (300)

Arsenic Poisoning-Induced Sensorineural Hearing Loss: A Case Report

open access: yes
Arsenic is frequently used in alternative medicine, and it is critical to promptly identify and treat suspected arsenic toxicity in patients. In a case study, a female patient presented with several symptoms, including nausea, vomiting, bilateral ...
Xinxin Yang   +3 more
core   +1 more source

Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case‐Series and Literature Review

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Sangeetha Yoganathan   +14 more
wiley   +1 more source

Factors predicting postoperative unilateral and bilateral speech recognition in adult cochlear implant recipients with acoustic hearing

open access: yes, 2016
Objectives: The first objective was to examine factors that could be predictive of postoperative unilateral (cochlear implant alone) speech recognition ability in a group of subjects with greater degrees of preoperative acoustic hearing than has been ...
Cowan, Robert   +4 more
core   +1 more source

Long‐Term Outcomes of Deep Brain Stimulation in Woodhouse–Sakati Syndrome

open access: yesMovement Disorders, EarlyView.
Abstract Background Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disease with distinctive neuroendocrine manifestations, with dystonia being the most common. No clear guidelines are available for the treatment of dystonia in WSS. Objective The aim was to analyze the impact of deep brain stimulation (DBS) on WSS‐associated dystonia ...
Hend Alhodaif   +5 more
wiley   +1 more source

Central Nervous System Tumors in Xeroderma Pigmentosum: Five Cases and Review of the Literature

open access: yesMovement Disorders, EarlyView.
Abstract Background Xeroderma pigmentosum (XP) is a rare autosomal recessive DNA‐repair disorder characterized by extreme ultraviolet radiation (UVR) sensitivity, markedly increased cutaneous malignancy risk, and progressive neurological disease in approximately one‐third of patients.
Farrah S. Bakr   +4 more
wiley   +1 more source

Hearing Screening in Neonatal Division (Levels II and III) in Amirkola Children Hospital

open access: yesMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2011
BACKGROUND AND OBJECTIVE: Hearing loss is one of the most important morbidities in high risk neonates admitted to NICU and special care nursing. This study was carried out to screen and follow up for hearing impairment in neonates who treated and ...
Y Zahedpasha   +3 more
doaj  

Bilateral bone conduction devices: improved hearing ability in children with bilateral conductive hearing loss

open access: yes, 2013
Item does not contain fulltextOBJECTIVES: The aim of the study was to investigate whether children with bilateral conductive hearing loss benefit from their second device (i.e., the bilateral bone conduction device [BCD]).
Snik, A.F.M.   +4 more
core  

SimulScan and Partial Least Squares: Visualizing Swallowing Through Functional and Dynamic Imaging Correlations

open access: yesMagnetic Resonance in Medicine, EarlyView.
ABSTRACT Purpose Swallowing involves the precise coordination of muscles and brain areas and can be disrupted in a variety of neurological conditions. Current methods to visualize swallowing cannot examine both the biomechanics and brain activity associated with specific swallowing events.
Bradley P. Sutton   +9 more
wiley   +1 more source

Canal Cholesteatoma Presentation and Management: A Systematic Review and Meta‐Analysis

open access: yesOtolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective To evaluate current understanding of external auditory canal cholesteatoma (EACC), its symptomatic burden, clinical features, diagnostic approach, and management strategies to reduce delays in diagnosis. Data Sources PubMed, CINAHL, COCHRANE Library, and SCOPUS.
Angelica M. Walker   +6 more
wiley   +1 more source

Longitudinal Cochlear Implant Use in Pediatric Patients With Unilateral Hearing Loss

open access: yesOtolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective To characterize longitudinal cochlear implant (CI) usage patterns in children with unilateral hearing loss (UHL) and evaluate the impact of age at implantation and duration of deafness on device use. Study Design Retrospective cohort study. Setting Two academic tertiary care centers. Methods Pediatric CI recipients with UHL implanted
David Octeau   +5 more
wiley   +1 more source

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