Results 41 to 50 of about 8,073 (133)

Steroids and idiopathic sudden sensorineural hearing loss in Songklanagarind Hospital

open access: yesJournal of Health Science and Medical Research (JHSMR), 2002
Objective: To study the effect of steroids on idiopathic sudden sensorineural hearing loss Material and Methods: Idiopathic sudden sensorineural hearing loss (ISHL) cases from 1998-2001 were collected and reviewed for demographic data, especially the ...
W Khaimook
doaj  

Hearing loss as the first symptom of pneumonia caused by Chlamydia psittaci: a case report and literature review

open access: yesBMC Infectious Diseases
Background The typical clinical symptoms of psittacosis pneumonia include fever, dry cough, and chills. Sudden sensorineural hearing loss is a relatively uncommon condition in pneumonia caused by Chlamydia psittaci. In this study, we reported a rare case
Huan-Huan Wu   +4 more
doaj   +1 more source

Longitudinal Cochlear Implant Use in Pediatric Patients With Unilateral Hearing Loss

open access: yesOtolaryngology–Head and Neck Surgery, Volume 175, Issue 2, Page 470-479, August 2026.
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

Treatment of idiopathic sudden sensorineural hearing loss with press needle

open access: yesJournal of the Pakistan Medical Association
Objective: To compare the effects of conventional therapy and press needle combined therapy on idiopathic sudden sensorineural hearing loss. Method: The retrospective case-control study was conducted from December 2023 to January 2024 at Department of
Feng Qin   +5 more
doaj   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken   +4 more
wiley   +1 more source

Mendelian Randomization Analysis of Human Blood Metabolites and Sensorineural Hearing Loss

open access: yesBrain and Behavior, Volume 16, Issue 7, July 2026.
ABSTRACT Objectives The role of the human blood metabolites and sensorineural hearing loss (SNHL) has been extensively studied, but the exact causal relationship remains uncertain. To address this knowledge gap, two‐sample Mendelian randomization (MR) analysis was employed to investigate the potential causal effects of blood metabolites on the risk of ...
Xingxing Ye   +6 more
wiley   +1 more source

Sudden Sensorineural Hearing Loss; Prognostic Factors [PDF]

open access: yesIranian Journal of Otorhinolaryngology, 2015
Introduction: Sudden sensorineural hearing loss (SSNHL) is a frightening and frustrating symptom for the patient as well as the physician. Prognosis is affected by multiple factors including duration of hearing loss, presence of associated vertigo and ...
Arjun Dass   +3 more
doaj  

Sudden hearing loss caused by labyrinthine hemorrhage

open access: yesBrazilian Journal of Otorhinolaryngology, 2008
Summary: Sudden sensorineural hearing loss is relatively frequent. In most cases, the etiology is not discovered. One of the possible causes for sudden deafness is inner labyrinth bleeding, which was difficult to diagnose before the advent of magnetic ...
Raquel Salomone   +5 more
doaj   +1 more source

Vitamin‐Responsive Disorders: From Molecular Basis to Clinical Presentation and Therapy

open access: yesJournal of Inherited Metabolic Disease, Volume 49, Issue 4, July 2026.
ABSTRACT Vitamin‐dependent cofactors are essential for numerous metabolic reactions, and defects affecting their uptake, conversion, utilisation, or regeneration constitute a heterogeneous group of inherited metabolic disorders (IMDs). Although dietary vitamin intake is sufficient to sustain coenzyme synthesis in healthy individuals, it is insufficient
Cécile Acquaviva   +5 more
wiley   +1 more source

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