Search results for "Hearing"

showing 10 items of 473 documents

Does tinnitus distress depend on age of onset?

2011

Objectives: Tinnitus is the perception of a sound in the absence of any physical source of it. About 5–15% of the population report hearing such a tinnitus and about 1–2% suffer from their tinnitus leading to anxiety, sleep disorders or depression. It is currently not completely understood why some people feel distressed by their tinnitus, while others don’t. Several studiesindicate that the amount of tinnitus distress is associated with many factors including comorbid anxiety, comorbid depression, personality, the psychosocial situation, the amount of the related hearing loss and the loudness of the tinnitus.Furthermore, theoretical considerations suggest an impact of the age at tinnitus o…

MaleAgingAnatomy and PhysiologyDatabases Factuallcsh:Medicine10045 Clinic for OtorhinolaryngologyAudiologySocial and Behavioral SciencesTinnitusddc:150GermanySurveys and QuestionnairesPsychologyAge of Onsetlcsh:ScienceDepression (differential diagnoses)PsychiatryAged 80 and overeducation.field_of_studyMultidisciplinaryDDC 150 / PsychologyTinnitus auriumAge FactorsAudiologyMiddle AgedSensory SystemsDistressMental HealthAuditory SystemAnxietyMedicineSensory PerceptionFemaleAltermedicine.symptomPsychosocialResearch ArticleAdultmedicine.medical_specialtyAdolescentHearing lossPopulationPsychological Stress610 Medicine & health1100 General Agricultural and Biological SciencesOhrgeräuschYoung Adult1300 General Biochemistry Genetics and Molecular Biologymedicineotorhinolaryngologic diseasesHumanseducationBiologyAgedComputational Neuroscience1000 MultidisciplinaryEvolutionary BiologyPopulation Biologybusiness.industryMood Disorderslcsh:RComputational BiologyHearing lossLogistic ModelsOtorhinolaryngologylcsh:QAge of onsetbusinessPhysiological ProcessesHörstörungOrganism DevelopmentTinnitusDevelopmental BiologyNeuroscience
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Hearing in Real-Life Environments (HERE) : Structure and Reliability of a Questionnaire on Perceived Hearing for Older Adults

2019

Supplemental Digital Content is available in the text.

MaleAgingIntraclass correlationHealth StatusvanhuksetAudiologyIntelligibility (communication)01 natural sciencesspeech perception0302 clinical medicineHearingSurveys and Questionnaires030223 otorhinolaryngology010301 acousticshuonokuuloisuusAged 80 and overSpeech perceptionikäkuulota3142Social ParticipationkuuloHearing levelTest scoreComputingMethodologies_DOCUMENTANDTEXTPROCESSINGAuditory PerceptionFemalemedicine.symptomPsychologyikääntyneetResearch Articlemedicine.medical_specialtySpeech perceptionHearing loss03 medical and health sciencesSpeech and HearingCronbach's alpha0103 physical sciencesmedicineotorhinolaryngologic diseasesHumansSound LocalizationHearing Lossquestionnaire validationOrientation SpatialAgedagingReproducibility of ResultsQuestionnaire validationta3125ikääntyminenOtorhinolaryngologyhearingStandardized coefficientQuality of LifeSelf ReportFactor Analysis StatisticalCOSMIN criteria
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Changes in hearing in 80-year-old people: a 10-year follow-up study

2004

The aims of this prospective 10-year longitudinal population study were to report changes in hearing in people aged 80 years at baseline, and to assess such changes by comparing results from both cross-sectional and longitudinal analyses. The study population comprised all residents of the city of Jyväskylä born in 1910 (n = 291). The subjects' hearing was tested on three occasions at 5-year intervals with the use of pure-tone audiometry, speech audiometry, and self-report on hearing difficulties. The results showed a significant deterioration in hearing sensitivity in both the longitudinal and cross-sectional assessments over the 10-year follow-up. However, the change in self-assessed hear…

MaleAgingLinguistics and Languagemedicine.medical_specialtyLongitudinal studyCross-sectional studyAudiologyLanguage and LinguisticsSpeech and HearingHearing AidsAcquired immunodeficiency syndrome (AIDS)Moderate hearing impairmentSurveys and Questionnairesotorhinolaryngologic diseasesmedicineHumansLongitudinal StudiesProspective StudiesHearing LossAgedAged 80 and overmedicine.diagnostic_test10 year follow upbusiness.industryAge Factorsmedicine.diseaseCross-Sectional StudiesAudiometry Pure-TonePopulation studyFemalePure tone audiometryAudiometryAudiometry SpeechbusinessBone ConductionInternational Journal of Audiology
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Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing…

2008

A homozygous reciprocal translocation, 46,XY,t(10;11),t(10;11), was detected in a boy with non-syndromic congenital sensorineural hearing impairment. Both parents and their four other children were heterozygous translocation carriers, 46,XX,t(10;11) and 46,XY,t(10;11), respectively. Fluorescence in situ hybridization of region-specific clones to patient chromosomes was used to localize the breakpoints within bacterial artificial chromosome (BAC) RP11-108L7 on chromosome 10q24.3 and within BAC CTD-2527F12 on chromosome 11q23.3. Junction fragments were cloned by vector ligation and sequenced. The chromosome 10 breakpoint was identified within the PDZ domain containing 7 (PDZD7) gene, disrupti…

MaleCandidate geneHeterozygoteUsher syndromePDZ domainMolecular Sequence DataChromosomal translocationBiologyTranslocation GeneticConsanguinityotorhinolaryngologic diseasesGeneticsmedicineHumansAmino Acid SequenceHearing LossMolecular BiologyGenetics (clinical)GeneticsGene RearrangementBacterial artificial chromosomemedicine.diagnostic_testBase SequenceChromosomes Human Pair 10Chromosomes Human Pair 11BreakpointHomozygoteChromosomeGeneral Medicinemedicine.diseaseMolecular biologyPedigreeChild PreschoolEar InnerFemaleUsher SyndromesFluorescence in situ hybridizationHuman molecular genetics
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Speech perception outcomes after cochlear implantation in prelingually deaf infants: The Western Sicily experience

2013

Objectives: To describe audiometric characteristics and speech perception performances of prelingually deaf Sicilian children after cochlear implantation; to identify the influence of cochlear implant (CI) user and family's characteristics on speech recognition and intelligibility outcomes. Methods: Twenty-eight infants with a congenital or acquired hearing impairment and implanted before the 3rd year of life were studied; all children suffered from bilateral sensorineural hearing loss (SNHL) with evidence of lack of hearing aids benefit and no evidence of intellectual disability. The study of the main characteristics associated with CI user and family's profile was performed with a clinica…

MaleCochlear implant Deaf children Sensorineural hearing loss Speech perception Speech intelligibilitymedicine.medical_specialtySpeech perceptionHearing lossmedicine.medical_treatmentHearing Loss SensorineuralIntelligibility (communication)AudiologyDeafnessAudiometryCochlear implantSurveys and QuestionnairesIntellectual disabilityotorhinolaryngologic diseasesmedicineHumansSicilymedicine.diagnostic_testbusiness.industrySpeech IntelligibilityInfantGeneral Medicinemedicine.diseaseCochlear ImplantationCochlear ImplantsTreatment OutcomeOtorhinolaryngologyPediatrics Perinatology and Child HealthCohortSpeech PerceptionSensorineural hearing lossFemaleAudiometrymedicine.symptombusiness
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Deficient membrane integration of the novel p.N14D-GJB2mutant associated with non-syndromic hearing impairment

2006

Mutations in GJB2, the gene encoding for the Gap Junction protein Connexin 26 (Cx26), have been established as the major cause of hereditary, non-syndromic hearing impairment (HI). We report here the identification of a novel point mutation in GJB2, c.40A>G [p.N14D], detected in compound heterozygosity with the c.35delG mutation in two brothers with moderate non-syndromic sensorineural HI. The mother who carried one wildtype and a p.N14D allele displayed normal hearing. The mutation leads to substitution of the neutral amino acid asparagine (N) by the negatively charged aspartic acid (D) at amino acid number 14, a position that is conserved among Cx26 of different organisms and among many o…

MaleDNA Mutational AnalysisMutantGene ExpressionConnexinIn Vitro TechniquesBiologymedicine.disease_causeCompound heterozygosityConnexinsXenopus laevisAspartic acidotorhinolaryngologic diseasesGeneticsmedicineAnimalsHumansCloning MolecularChildHearing LossGenetics (clinical)chemistry.chemical_classificationMutationPoint mutationCell MembraneWild typeGap JunctionsMolecular biologyPedigreeAmino acidConnexin 26Protein TransportchemistryChild PreschoolAntigens SurfaceMutationOocytesHuman Mutation
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Born to dance but beat deaf: A new form of congenital amusia

2011

Humans move to the beat of music. Despite the ubiquity and early emergence of this response, some individuals report being unable to feel the beat in music. We report a sample of people without special training, all of whom were proficient at perceiving and producing the musical beat with the exception of one case (“Mathieu”). Motion capture and psychophysical tests revealed that people synchronized full-body motion to music and detected when a model dancer was not in time with the music. In contrast, Mathieu failed to period- and phase-lock his movement to the beat of most music pieces, and failed to detect most asynchronies of the model dancer. Mathieu’s near-normal synchronization with a…

MaleDanceCognitive NeuroscienceExperimental and Cognitive PsychologyMetronomeMusicalAmusiabehavioral disciplines and activitiesMotion capture050105 experimental psychologylaw.invention03 medical and health sciencesBehavioral NeuroscienceYoung Adult0302 clinical medicineRhythmlawmedicineHumans0501 psychology and cognitive sciencesDancingCommunicationBeat deafnessbusiness.industry05 social sciencesAuditory Perceptual Disordersmedicine.diseasehumanitiesPersons With Hearing Impairmentsta6131Auditory PerceptionbusinessPsychologyhuman activitiesBeat (music)030217 neurology & neurosurgeryMusicCognitive psychologyNeuropsychologia
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Interrogator intonation and memory encoding performance.

2019

Based on recent findings that interrogator intonation can enhance interrogative suggestibility during recall phases, the present study tested influences of interrogator intonation on memory performance even as early as at the encoding stage. We experimentally manipulated interrogator intonation during encoding of a story to be recalled in immediate and delayed subsequent memory tests (Experiment 1, N = 50). As expected, a symmetrically structuring vs. an isolating-emphasizing speaking style generally increased the amount of freely recalled details. In a more fine-grained experiment (N = 50), we additionally manipulated emphasized story details and tested recall rates for peripheral, neutral…

MaleEmotionsSocial SciencesCognitionLearning and MemoryHearingMedicine and Health SciencesPsychologyInterrogationPitch PerceptionLanguageGrammarMultidisciplinary05 social sciencesQRCognitionSyllablesClinical Laboratory SciencesMemory RecallEngineering and TechnologyMedicineSensory PerceptionFemalePsychologyCognitive psychologyResearch ArticleAdultSciencePhonologyEffect Modifier Epidemiologic050105 experimental psychologyYoung AdultMemoryDiagnostic MedicineEncoding (memory)SpeechHumans0501 psychology and cognitive sciencesRelevance (information retrieval)0505 lawForensicsRecallVerbal BehaviorSuggestibilityIntonation (linguistics)Cognitive PsychologyBiology and Life SciencesLinguisticsInterrogativeSpeech Signal ProcessingSignal ProcessingMental Recall050501 criminologyCognitive ScienceLaw and Legal SciencesNeurosciencePLoS ONE
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Electrical brain activity and facial electromyography responses to irony in dysphoric and non-dysphoric participants

2020

We studied irony comprehension and emotional reactions to irony in dysphoric and control participants. Electroencephalography (EEG) and facial electromyography (EMG) were measured when spoken conversations were presented with pictures that provided either congruent (non-ironic) or incongruent (ironic) contexts. In a separate session, participants evaluated the congruency and valence of the stimuli. While both groups rated ironic stimuli funnier than non-ironic stimuli, the control group rated all the stimuli funnier than the dysphoric group. N400-like activity, P600, and EMG activity indicating smiling were larger after the ironic stimuli than the non-ironic stimuli for both groups. Further…

MaleFacial MusclesElectroencephalographyAudiologyevent-related potentialsLanguage and Linguisticsdepressive symptoms0302 clinical medicineironiaN400Evoked Potentialsmedia_commonP600ironymedicine.diagnostic_testDepressionCommunication05 social sciencesBrainElectroencephalographyIronyFacial ExpressionelektromyografiaFemaleComprehensionPsychologyFacial electromyographymasennusAdultLinguistics and Languagemedicine.medical_specialtyCognitive Neurosciencemedia_common.quotation_subjectExperimental and Cognitive Psychologyfacial electromyography050105 experimental psychologyLateralization of brain functionYoung Adult03 medical and health sciencesSpeech and HearingtunteetEvent-related potentialmedicineP600Humans0501 psychology and cognitive sciencesilmeetValence (psychology)ElectromyographyComprehension030217 neurology & neurosurgeryBrain and Language
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A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression

2010

Contains fulltext : 87760_1.pdf (author's version ) (Open Access) Contains fulltext : 87760_2.pdf (Publisher’s version ) (Closed access) Eleven affected members of a large German-American family segregating recessively inherited, congenital, non-syndromic sensorineural hearing loss (SNHL) were found to be homozygous for the common 35delG mutation of GJB2, the gene encoding the gap junction protein Connexin 26. Surprisingly, four additional family members with bilateral profound SNHL carried only a single 35delG mutation. Previously, we demonstrated reduced expression of both GJB2 and GJB6 mRNA from the allele carried in trans with that bearing the 35delG mutation in these four persons. Usin…

MaleGenetics and epigenetic pathways of disease [NCMLS 6][SDV]Life Sciences [q-bio]PenetranceMESH: Base SequenceRegulatory Sequences Nucleic Acidsensorineural hearing lossConnexinsMESH: GenotypeMESH: Hearing Loss Sensorineural/diagnosisMESH: PenetranceGenotypeCopy-number variationGenetics (clinical)Sequence DeletionGeneticsComparative Genomic Hybridization0303 health sciencesMESH: Genetic TestingMESH: Gene Expression Regulation*030305 genetics & heredityPenetranceGJB2PedigreeConnexin 26MESH: Sequence Deletion*MESH: Hearing Loss Sensorineural/geneticsFemaleChromosome DeletionFunctional Neurogenomics [DCN 2]GJB6GenotypeMESH: PedigreeMESH: Chromosome DeletionHearing Loss SensorineuralMolecular Sequence Dataconnexin 26connexin 30DFNB1gene expression regulationGJB2GJB6sensorineural hearing losssequence deletionBiologyMESH: Connexin 30MESH: Connexins/genetics*MESH: Sequence Homology Nucleic AcidArticleGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesMonoallelic MutationGJB6MESH: Connexin 26Sequence Homology Nucleic AcidConnexin 30otorhinolaryngologic diseasesGeneticsHumansGenetic TestingAlleleGeneMESH: Regulatory Sequences Nucleic Acid/genetics*AllelesDFNB1030304 developmental biologyFamily HealthMESH: HumansMESH: Molecular Sequence DataBase SequenceChromosomes Human Pair 13MESH: AllelesBreakpointMESH: MaleMESH: Comparative Genomic HybridizationGene Expression RegulationMESH: Family Healthbiology.proteinHuman medicineMESH: Chromosomes Human Pair 13/geneticsMESH: FemaleClinical Genetics
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