Results 261 to 270 of about 87,262 (329)

Sudden Sensorineural Hearing Loss in an Immunocompetent Patient With West Nile Encephalitis

open access: yesLaryngoscope Investigative Otolaryngology, Volume 10, Issue 4, August 2025.
ABSTRACT Objective Sudden sensorineural hearing loss (SSNHL) is a frequently encountered condition that is often idiopathic but may be precipitated by infection. Neuroinvasive disease resulting from West Nile virus (WNV) is a rare cause of SSNHL, typically affecting immunocompromised patients and generally associated with minimal hearing recovery.
Raj Malhotra   +3 more
wiley   +1 more source

Ongoing Discrepancy Between Unilateral Meniere's Disease and Bilateral Endolymphatic Hydrops on Hydrops MRI

open access: yesLaryngoscope Investigative Otolaryngology, Volume 10, Issue 4, August 2025.
ABSTRACT Objective In the era of Hydrops MRI, a clinical dilemma has emerged: while Meniere's disease (MD) is diagnosed unilaterally, Hydrops MRI demonstrates endolymphatic hydrops (EH) bilaterally. This study aims to clarify this ongoing discrepancy. Methods Fifty‐six MD patients underwent an inner ear test battery followed by 3 T Hydrops MRI.
Ting‐Hua Yang   +2 more
wiley   +1 more source

The Relationship Between Daily Device Use and Subjective Hearing Abilities in Pediatric Cochlear Implant Users

open access: yesOtolaryngology–Head and Neck Surgery, Volume 173, Issue 2, Page 505-511, August 2025.
Abstract Objective Increased hours of cochlear implant (CI) use have been shown to improve auditory and speech recognition outcomes in children with hearing loss. However, the impact of hours of CI use over time on patient‐reported functional hearing skills is unknown.
Lacey Magee   +3 more
wiley   +1 more source

Wilms Tumor in Children With AMER1/WTX Germline Pathogenic Variants: A Multicenter Case Series

open access: yesPediatric Blood &Cancer, Volume 72, Issue 8, August 2025.
ABSTRACT Background 10–15% of children with Wilms tumor (WT) have predisposing genetic syndromes. Somatic mutations are frequently identified; however, germline pathogenic variants in AMER1 are much less prevalent and are associated with osteopathia striata with cranial sclerosis (OSCS).
Insiyah Campwala   +9 more
wiley   +1 more source

Academic achievement of children with unilateral or mild bilateral hearing loss: A systematic review

open access: yesReview of Education, Volume 13, Issue 2, August 2025.
Abstract There has been significant research on the association between hearing loss and academic achievement. However, many studies do not disaggregate by degree of hearing loss. Therefore, the risks to school performance posed by unilateral and mild bilateral hearing loss are not well understood, despite prevalence studies suggesting that 2.4 to 23 ...
Katherine Collier
wiley   +1 more source

The Natural Course of Bosch‐Boonstra‐Schaaf Optic Atrophy Syndrome

open access: yesClinical Genetics, Volume 108, Issue 2, Page 168-178, August 2025.
Here, we present data on genetic variants and phenotype development of 47 individuals with Bosch‐Boonstra‐Schaaf optic atrophy syndrome, a rare neurodevelopmental disorder, highlighting the fact that the disease does not appear to be fundamentally progressive.
Ilia Valentin   +4 more
wiley   +1 more source

Vitiligo

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 8, Page 968-987, August 2025.
Summary Vitiligo is a common pigment disorder of the skin resulting in destruction of melanocytes. Non‐segmental vitiligo (NSV) is an autoimmune disorder. The etiopathogenesis of segmental vitiligo (SV) remains incompletely understood. Genetic predisposition and increased vulnerability of melanocytes towards stressors lead to a melanocyte‐specific CD8+
Markus Böhm, Adrian Tanew
wiley   +1 more source

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