Results 241 to 250 of about 87,827 (343)

Cortical Structure Abnormalities in Patients With Noise‐Induced Hearing Loss: A Surface‐Based Morphometry Study

Brain and Behavior, Volume 15, Issue 9, September 2025.
•To investigate the characteristics of brain structures in patients with noise‐induced hearing loss (NIHL) using source‐based morphometry (SBM). •To evaluate the correlation between abnormal brain regions and clinical data. •On the basis of the SBM method, complex cortical structural alterations in patients with NIHL predominantly involved the parietal
Yunxin Li, Ranran Huang, Aijie Wang, Liping Wang, Minghui Lv, Xianghua Bao, Guowei Zhang   +6 more
wiley   +1 more source

Central nervous system superficial siderosis: A case report and literature review. [PDF]

Medicine (Baltimore)
Xu Q, Wen S, Li H, Yang G, Di M.
europepmc   +1 more source

Lupus Anticoagulant Induced Sudden Profound Sensorineural Hearing Loss.

, 1991
Kazutaka Hisashi, S. Komune, Toshiaki Taira, Seizo Sadoshima   +3 more
openalex   +2 more sources

Prenatal Diagnosis of Bartter Syndrome: Lessons From a Complex Diagnostic Procedure

Clinical Case Reports, Volume 13, Issue 9, September 2025.
ABSTRACT Bartter syndrome is an idiopathic condition that may manifest antenatally, characterized by a spectrum of symptoms including maternal polyhydramnios, prematurity, polyuria, hypercalciuria, nephrocalcinosis, normomagnesemia, vomiting, growth retardation, and elevated renal synthesis and urinary excretion of prostaglandins.
Athina A. Samara, Paschalis Mousios, Paraskevas Perros, Antonios Koutras, Emmanouil Manolakos, Eleftherios Anastasakis, Chara Skentou, Konstantinos Dafopoulos, Antonios Garas, Sotirios Sotiriou   +9 more
wiley   +1 more source

Sensorineural deafness in a child with Prader-Willi Syndrome-A rare case report. [PDF]

J Family Med Prim Care
Saikrishna P, Tripathy SK, Medhagopal RG, Das S, Bharti B, Malik A.   +5 more
europepmc   +1 more source

Evaluation of Acute Low Tone Sensorineural Hearing Loss utilizing Evoked Otoacoustic Emissions.

, 1994
Taku Hattori, Niang Dan Qiu, Masayuki Sawaki, Hiromi Ueda, Noriyuki Yanagita, Hideto Niwa   +5 more
openalex   +2 more sources

Identification of A Novel Mutation of SHORT Syndrome: A Case Report

Clinical Case Reports, Volume 13, Issue 9, September 2025.
ABSTRACT SHORT syndrome is a rare inherited disease with 34 identified pathogenic or likely pathogenic PIK3R1 mutations. The genotype–phenotype relationship remains inconsistent. Our case presents the first novel duplication that affects up to 25 nucleotides and truncates the PI3K protein, contributing valuable data to genetic understanding and ...
Quynh Thi Vu Huynh, Tuong Trong Luong, Ho Tran Ban, Van Tran   +3 more
wiley   +1 more source

<i>WFS1</i> gene mutation associated with pediatric diabetes mellitus and congenital deafness: A case report. [PDF]

World J Diabetes
Gao AM, Deng WL, Yang XP, Wu WY, Ma CY, Liu Y.   +5 more
europepmc   +1 more source

The Long Term Follow Up by Questionnaire for Acute Low-tone Sensorineural Hearing Loss

, 1992
Shiro Iwabuchi, Kazuo Matsui, Michihiko Nozue   +2 more
openalex   +2 more sources

Stroke Mimicry: Unmasking a Brainstem Tuberculoma in a Young Patient

Clinical Case Reports, Volume 13, Issue 9, September 2025.
A young male presented with stroke‐like symptoms ‐ progressive hemiparesis and cranial nerve palsies. MRI brain revealed a ring‐enhancing intrapontine lesion with perilesional edema, suggestive of tuberculoma. Early initiation of anti‐tubercular therapy led to complete recovery.
Nithish Nanda Palanisamy, Dhiran Sivasubramanian, Virushnee Senthilkumar, Smrti Aravind, Sathwik Sanil, Karthick Balasubramanian   +5 more
wiley   +1 more source