Results 61 to 70 of about 9,309,566 (214)

Vestibular migraine or Meniere's disease: a diagnostic dilemma

open access: yesJournal of Neurology, 2022
Meniere’s disease (MD) represents one of the vertigo disorders characterized by triad symptoms (recurrent vertigo, fluctuating hearing loss, tinnitus or ear fullness). The diagnosis of MD relies on the accurate and detailed taking of medical history, and
Jing-Yu Chen   +7 more
semanticscholar   +1 more source

Anxiety and Depression in Adults With Vestibular Disorders: A Systematic Review and Meta‐Analysis

open access: yesThe Laryngoscope, Volume 136, Issue 2, Page 535-546, February 2026.
This systematic review and meta‐analysis of 85 studies (n = 764,403) found that adults with vestibular disorders have markedly higher rates and risks of anxiety and depression than controls. Prevalence was greatest in episodic conditions such as vestibular migraine and Ménière's disease.
Cory Hyun‐su Kim   +5 more
wiley   +1 more source

Evaluation of quality of life pre- and post-vestibular rehabilitation in patients with benign paroxysmal positional vertigo associated with Meniere's disease

open access: yesInternational Archives of Otorhinolaryngology, 2012
Summary Introduction: Vertigo is a symptom that impacts the patients' quality of life and may force them to cease performing activities of daily living. Here, we discuss benign paroxysmal positional vertigo (BPPV) and Meniere's disease (MD),
Dayra Dill Socher   +2 more
doaj   +3 more sources

Incipient Ménière disease: one case report

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2021
doi:10.3969/j.issn.1672⁃6731.2021.02 ...
REN Tong⁃li, WANG Wu⁃qing
doaj  

Profound Cognitive Impairment as a Salient Feature of Multiple Sclerosis: A Case Report

open access: yesClinical and Experimental Neuroimmunology, Volume 17, Issue 1, February 2026.
ABSTRACT Background Cognitive impairment affects up to two‐thirds of patients with multiple sclerosis (MS); however, profound global deficits, defined as a full‐scale IQ below 70, are uncommon and rarely constitute the primary symptom. Case Presentation We describe a 27‐year‐old woman with severe multidomain cognitive impairment due to MS ...
Shota Ito   +3 more
wiley   +1 more source

A membranous nephropathy variant mimicking minimal change disease

open access: yesThe Journal of Pathology: Clinical Research, Volume 12, Issue 1, January 2026.
Abstract This study characterizes a novel disease pattern of membranous nephropathy (MN) that exhibits overlapping clinicopathological features with minimal change disease (MCD), termed ‘MCD‐like MN’. Patients with histologically confirmed MN showing sparse and segmental subepithelial electron‐dense deposits (EDD) but clinically resembling MCD were ...
Chuqi Pan   +8 more
wiley   +1 more source

Membrane Stress Proclivities in the Mammalian Labyrinth

open access: yesInternational Archives of Otorhinolaryngology, 2014
Introduction The membranes of the inferior division of the labyrinth in some mammals appear more vulnerable to hydropic distention than those of the superior division.
Daniel J. Pender
doaj   +1 more source

Vitamin D Deficiency as a Risk Factor for Onset and Recurrence of Sudden Sensorineural Hearing Loss: A Prospective Cohort Study With Age‐Specific Analysis

open access: yesFood Science &Nutrition, Volume 14, Issue 1, January 2026.
Pure‐tone audiometry (0–120 dB HL) identified patients with sudden sensorineural hearing loss (SSNHL). Serum 25‐hydroxyvitamin D levels revealed deficient (< 20 ng/mL), insufficient (20–30 ng/mL), or sufficient (≥ 30 ng/mL) status. Novel findings demonstrate low vitamin D correlates with higher SSNHL onset/recurrence, particularly elevating risk in ...
Qi Hui   +8 more
wiley   +1 more source

A Case of Cystic Fibrosis in a Japanese Man With Congenital Bilateral Absence of the Vas Deferens and Recurrent Pancreatitis Caused by a Homozygous c.1210‐11 T > G Variant of the Cystic Fibrosis Transmembrane Conductance Regulator Gene

open access: yesReproductive Medicine and Biology, Volume 25, Issue 1, January/December 2026.
ABSTRACT Case We herein report a rare case of a Japanese man diagnosed with cystic fibrosis (CF) following a workup for male infertility and recurrent pancreatitis and discuss the clinical and diagnostic implications in a population wherein CF is exceptionally rare. A 27‐year‐old Japanese man who presented with azoospermia underwent clinical evaluation,
Tomoki Saito   +9 more
wiley   +1 more source

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