Results 31 to 40 of about 1,567 (195)

Analysis of GJB2 (Connexin 26) Mutation in Patients with Congenital Non-Syndromic Sensorineural Hearing Loss

open access: yesTurkish Archives of Otorhinolaryngology, 2014
Objective:This study was performed to investigate the GJB2 (connexin 26) gene mutations that are the most frequent cause of sensorineural deafness in patients with congenital non-syndromic sensorineural hearing loss in our region.Methods:Sixty patients ...
Emin Kaskalan   +6 more
doaj   +1 more source

Nasal Malignant Melanoma With an Inverted Papilloma in the Contralateral Nasal Cavity: A Case Report

open access: yesEar, Nose & Throat Journal
Background: We describe a patient with sinonasal mucosal melanoma (SNMM) and an inverted papilloma, which existed independently in both nasal cavities. Case presentation: We describe an unusual case of a 74-year-old male patient with SNMM and an inverted
Jing Guo MD   +5 more
doaj   +1 more source

Chronic Cough in Otorhinolaryngologic Routine

open access: yes, 2011
SummaryIntroduction: The chronic cough is sometimes manifested as an imprecise symptom, but of great importance for both the diagnosis and the prognosis.
Camilo Ferreira Ramos   +11 more
core   +1 more source

Anlotinib suppressed tumor cell proliferation and migration in hypopharyngeal carcinoma

open access: yesBrazilian Journal of Otorhinolaryngology
Objective: The purpose of this study is to study the in-vitro effects of multitarget inhibitor anlotinib on hypopharyngeal cancer cell proliferation and cell migration, and the underlying mechanism, which will provide new drug choices for hypopharyngeal ...
Hao Song   +6 more
doaj   +1 more source

Extrathyroidal Extension Prediction of Papillary Thyroid Cancer With Computed Tomography Based Radiomics Nomogram: A Multicenter Study

open access: yesFrontiers in Endocrinology, 2022
ObjectivesTo develop and validate a Computed Tomography (CT) based radiomics nomogram for preoperative predicting of extrathyroidal extension (ETE) in papillary thyroid cancer (PTC) patientsMethodsA total of 153 patients were randomly assigned to ...
Pengyi Yu   +21 more
doaj   +1 more source

Spontaneous Otogenic Intracranial Pneumocephalus: A Case Report

open access: yesEar, Nose & Throat Journal
Spontaneous otogenic pneumocephalus (SOP) is a rare condition. We report a case of SOP that may be related to repeated Valsalva maneuvers. A young woman underwent repeated Valsalva maneuvers to restore Eustachian tube function and subsequently developed ...
Yuwan Song PhD   +5 more
doaj   +1 more source

Fallopian canal arachnoid cyst with acute facial nerve paralysis in children: a report of two cases and literature review

open access: yesFrontiers in Neurology, 2023
IntroductionSymptoms induced by arachnoid cysts in the fallopian canal are uncommon, and facial nerve paralysis without cerebrospinal fluid otorrhea is comparatively rarer.MethodsHerein, we present two cases of arachnoid cysts in the fallopian canal with
Jianbin Sun   +5 more
doaj   +1 more source

Otorhinolaryngologic, head and neck presentations among patients with chronic renal disease in a developing country [PDF]

open access: yes, 2020
Background: Data on otorhinolaryngology and head and neck diseases in patient with chronic renal disease are rare in developing African countries. This study was aimed to determine the epidemiology and management of otorhinolaryngology and head and ...
Adegbiji, Waheed Atilade   +3 more
core  

Gut microbiota-metabolome crosstalk in allergic diseases: mechanistic insights and translational opportunities

open access: yesFrontiers in Allergy
The gut microbiota and its metabolites play important roles in the pathogenesis of various diseases. The diversity of the gut microbiota is closely related to the development and function of the human immune system.
HanBin Qin   +33 more
doaj   +1 more source

Osteopathia striata-cranial sclerosis: otorhinolaryngologic clinical presentation and radiologic findings

open access: yes, 2007
Background: Osteopathia striata with cranial sclerosis (OS-CS) is a rare bone dysplasia that presents with variable symptoms mainly due to the associated CS.
MARINI, Mario   +6 more
core   +1 more source

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