Search results for "Hearing"

showing 10 items of 473 documents

Hearing impairment and diverse health outcomes: An umbrella review of meta-analyses of observational studies

2021

Background: Globally, it is estimated that approximately 1.3 billion people live with some form of hearing impairment. Major causes of hearing loss include infection/disease, age-related factors, and occupational factors. Numerous systematic reviews and meta-analyses have attempted to synthesise literature on these topics. To date there has not been a systematic evaluation of the relationships between hearing impairment and diverse physical, mental, and social outcomes. Objective: We performed an umbrella review of systematic reviews of observational studies with meta-analyses for any physical disease, biomarkers of disease, mental health or cognitive outcomes, and/or modifiable risk factor…

Hearing lossHearing Loss Sensorineural[SDV]Life Sciences [q-bio]Disease030204 cardiovascular system & hematologyDeafnessHearing impairment03 medical and health sciencesUmbrella review0302 clinical medicineQuality of life (healthcare)Outcome Assessment Health Caremedicineotorhinolaryngologic diseasesHumans030212 general & internal medicineChildbusiness.industrys Hearing impairment Hearing loss Deaf Umbrella review DeafnessGeneral MedicineHearing lossmedicine.diseaseMental health3. Good healthSystematic reviewQuality of LifeObservational studySensorineural hearing lossmedicine.symptombusinessDeafTinnitusClinical psychologySystematic Reviews as Topic
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Do Sign Language Videos Improve Web Navigation for Deaf Signer Users?

2010

The efficacy of video-based sign language (SL) navigation aids to improve Web search for Deaf Signers was tested by two experiments. Experiment 1 compared 2 navigation aids based on text hyperlinks linked to embedded SL videos, which differed in the spatial contiguity between the text hyperlink and SL video (contiguous vs. distant). Deaf Signers’ performance was similar in Web search using both aids, but a positive correlation between their word categorization abilities and search efficiency appeared in the distant condition. In Experiment 2, the contiguous condition was compared with a text-only hyperlink condition. Deaf Signers became less disorientated (used shorter paths to find the tar…

Hearing lossInformation accessDeafnessSign languagecomputer.software_genreEducationSign LanguageSpeech and HearingmedicineHumansWeb navigationInternetbusiness.industryVideotape RecordingHyperlinkLinguisticsCategorizationComputingMilieux_COMPUTERSANDSOCIETYThe InternetArtificial intelligencemedicine.symptombusinessPsychologycomputerNatural language processingWord (computer architecture)Journal of Deaf Studies and Deaf Education
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Screening of the USH1G gene among Spanish patients with Usher syndrome. Lack of mutations and evidence of a minor role in the pathogenesis of the syn…

2007

The Usher syndrome (USH) is an autosomal recessive hereditary disorder characterized by the association of sensorineural hearing loss, retinitis pigmentosa (RP) and, in some cases, vestibular dysfunction. The USH1G gene, encoding SANS, has been found to cause both Usher syndrome type I and atypical Usher syndrome. 109 Spanish unrelated patients suffering from Usher syndrome type I, type II, type III and unclassified Usher syndrome were screened for mutations in this gene, but only eight different changes without a clear pathogenic effect have been detected. Based on these results as well as previous studies in other populations where mutational analysis of this gene has been carried out, on…

Hearing lossUsher syndromeDNA Mutational AnalysisMolecular Sequence DataNerve Tissue ProteinsPathogenesisRetinitis pigmentosaotorhinolaryngologic diseasesmedicineHumansAmino Acid SequenceGenetic TestingGeneGenetics (clinical)Geneticsbusiness.industrymedicine.diseaseeye diseasesMutational analysisOphthalmologySpainPediatrics Perinatology and Child HealthMutationSensorineural hearing lossmedicine.symptombusinessUsher SyndromesUSH1G GENEOphthalmic genetics
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Array-CGH and clinical characterization in a patient with subtelomeric 6p deletion without ocular dysgenesis

2011

Subtelomeric terminal 6p deletion has been recognized as a clinically identifiable syndrome including facial dysmorphism, malformation of the anterior eye chamber, hearing loss, heart defect and developmental delay. Genotype –phenotype correlations of previously published patients have been strongly suggested anterior eye segment anomalies as one of major malformation of the syndrome if the critical 6p25 region containing the FOXC 1 gene. In addition it has been hypothesized the presence in this region of one or more genes involved in hearing loss. We report on a case of terminal 6p deletion in a 47, XYY karyotype. Further characterization of the deletion with array comparative genome hybri…

Heart Defects CongenitalMaleHearing lossDevelopmental DisabilitiesKaryotypeBiologyEyeDysgenesisSettore MED/38 - Pediatria Generale E SpecialisticaChromosome 19GeneticsmedicineHumansarray-CGH.Eye AbnormalitiesGeneGenetics (clinical)Genetic Association StudiesIn Situ Hybridization FluorescenceGeneticsComparative Genomic Hybridizationeye abnormalitieInfantKaryotypeForkhead Transcription Factorshearing loSubtelomereAnterior Eye SegmentSettore MED/03 - Genetica MedicaChromosomes Human Pair 6FOXC1medicine.symptomChromosome Deletionchromosome 6p deletionComparative genomic hybridization
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Chronic otitis caused by heterotopic brain tissue in pterygopalatine fossa

2007

Summary Heterotopic brain tissue is a rare is congenital anomaly, it may present at any age but it is frequently in infancy. This anomaly can occur most frequently in nasal region, although rests elsewhere in the digestive tract, in facial tissue or in lungs have been reported. Heterotopic brain tissue has been defined as a mass composed of mature brain tissue, outside the cranial cavity or spinal canal. We present a 9 years old girl with history of left chronic otitis and nasal obstruction caused by heterotopic brain tissue in pterygopalatine fossa.

Heterotopic brain tissuebusiness.industryChronic otitisChronic otitisBrain tissueAnatomymedicine.diseaseConductive hearing lossConductive hearing lossParapharyngeal spacemedicine.anatomical_structureOtorhinolaryngologyNasal regionPediatrics Perinatology and Child HealthParapharyngeal spacemedicineCranial cavitySpinal canalbusinessGlue earPterygopalatine fossaInternational Journal of Pediatric Otorhinolaryngology Extra
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The discovery of stapes

2013

Giovanni Filippo Ingrassia revisited and redefined some of Galeno's reports, and was recognized as one of the leading Italian Physicians of the 16th century. Ingrassia principally studied the skull, and gave very important contributions to otorhinolaryngology, including the discovery of the stapes. He also isolated the inferior nasal concha from the maxillary bone, described the frontal sinus, the pterygopalatine fossa and several foramina of the skull. Ingrassia firstly attributed a sensorial function to the middle ear bones, which he called fifth particular function. He also added some details to the description of the VIII cranial nerve, which introduces the concept of bone conducting so…

HistoryHistory CornerOtologyEarHistoryOtologyStapes HearingIngrassiaEarStapesIngrassiaOtolaryngologyHearingItalyHistory 16th Centuryotorhinolaryngologic diseasesHumansActa Otorhinolaryngologica Italica
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Managing a Pan-European Consortium on Late Effects among Long-Term Survivors of Childhood and Adolescent Cancer—The PanCareLIFE Project

2021

PanCareLIFE brought together European partners and is the largest study to have evaluated the issues of fertility impairment, hearing loss, and health-related quality of life in survivors of childhood and adolescent cancer. Successful delivery of the project aims did not evolve solely from scientific qualities. Organizational structure and careful information management were key components for its successful completion and are retrospectively assessed in this paper. PanCareLIFE used cohort studies, case-control studies, clinical evaluation of hearing, and genetic testing to study 32,000 survivors from 25 data providers. A management team implemented the organizational structures, was the de…

Information managementAdolescentcancer survivorHealth Toxicology and Mutagenesismedicine.medical_treatmentlcsh:MedicineMedical OncologySupport groupArticle03 medical and health sciences0302 clinical medicineQuality of life (healthcare)BlueprintNeoplasmsHealth caremedicineHumanslate effectsSurvivors030212 general & internal medicineRetrospective Studieshearing lossfertilityMedical educationCancer survivorchildbusiness.industrylcsh:RPublic Health Environmental and Occupational Healthhealth carehealth-related quality of life030220 oncology & carcinogenesisQuality of LifeOrganizational structureepidemiologyBiostatisticsbusinessPsychologyInternational Journal of Environmental Research and Public Health
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Techniques of intratympanic administration

2010

Intratympanic administration desametasone hearing loss
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Literacy skills and online research and comprehension: struggling readers face difficulties online

2019

The present study evaluated the extent to which literacy skills (reading fluency, written spelling, and reading comprehension), together with nonverbal reasoning, prior knowledge, and gender, are related to students’ online research and comprehension (ORC) performance. The ORC skills of 426 sixth graders were measured using a Finnish adaptation of the Online Research and Comprehension Assessment. Results of a structural equation model showed that these ORC skills were divided into six highly correlated factors, and that they formed a common factor in ORC. Altogether, these predictor variables explained 57% of the variance in ORC. Reading comprehension, along with gender, was the strongest p…

Linguistics and Language4. Educationmedia_common.quotation_subject05 social sciences050301 educationOnline research methods050105 experimental psychologyLiteracySpellingEducationComprehensionSpeech and HearingNonverbal communicationFluencyNeuropsychology and Physiological PsychologyReading comprehensionReading (process)Mathematics education0501 psychology and cognitive sciencesPsychology0503 educationmedia_commonReading and Writing
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2016

The neural systems supporting speech and sign processing are very similar, although not identical. In a previous fTCD study of hearing native signers (Gutierrez-Sigut, Daws, et al., 2015) we found stronger left lateralization for sign than speech. Given that this increased lateralization could not be explained by hand movement alone, the contribution of motor movement versus ‘linguistic’ processes to the strength of hemispheric lateralization during sign production remains unclear. Here we directly contrast lateralization strength of covert versus overt signing during phonological and semantic fluency tasks. To address the possibility that hearing native signers’ elevated lateralization ind…

Linguistics and LanguageCognitive Neuroscience05 social sciencesSemantic fluencyExperimental and Cognitive PsychologySign language050105 experimental psychologyLanguage and LinguisticsLateralization of brain functionlanguage.human_languageMotor movement03 medical and health sciencesSpeech and Hearing0302 clinical medicineBritish Sign LanguageCovertLateralitylanguage0501 psychology and cognitive sciencesPsychologyPhonological encoding030217 neurology & neurosurgeryCognitive psychologyBrain and Language
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