Search results for " sensor"

showing 10 items of 1714 documents

New determinants of olfactory habituation

2017

AbstractHabituation is a filter that optimizes the processing of information by our brain in all sensory modalities. It results in an unconscious reduced responsiveness to continuous or repetitive stimulation. In olfaction, the main question is whether habituation works the same way for any odorant or whether we habituate differently to each odorant? In particular, whether chemical, physical or perceptual cues can limit or increase habituation. To test this, the odour intensity of 32 odorants differing in physicochemical characteristics was rated by 58 participants continuously during 120s. Each odorant was delivered at a constant concentration. Results showed odorants differed significantl…

MaleChemical Phenomenamedicine.medical_treatmentOlfaktorsystem Sensorische Verarbeitung Technische Universität Dresden PublikationsfondsStimulationstimulation0302 clinical medicinehomologous seriesHabituationmedia_commonCarbon chainMultidisciplinary05 social sciencesdésensibilisationOlfactory system Sensory processing Technsiche Unviersität Dresden Publishing FundhommeDesensitization (psychology)Smell[ SDV.MHEP.OS ] Life Sciences [q-bio]/Human health and pathology/Sensory OrgansAlimentation et Nutrition[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]Femalecortical adaptationPsychologypsychological phenomena and processesAdultmedia_common.quotation_subjectdesensitizationOlfaction050105 experimental psychologyArticleodorant receptor03 medical and health sciencesYoung AdultStimulus modalityPerceptionmedicineHumansFood and Nutrition0501 psychology and cognitive sciences[SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory OrgansHabituation Psychophysiologicrécepteur odorantidentification de l'odeurNeurosciencescortical adaptation;homologous series;odorant receptor;stimulation;responses;humans;desensitization;discrimination;identification;activationOdor[ SDV.NEU ] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]Neurons and CognitionOdorantsresponsesddc:520identificationactivationNeuroscience030217 neurology & neurosurgerydiscrimination
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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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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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Age, training, and previous experience predict race performance in long-distance inline skaters, not anthropometry

2012

Knechtle, Beat | Knechtle, Patrizia | Ruest, Christoph Alexander | Rosemann, Thomas | Lepers, Romuald; International audience; ''The association of characteristics of anthropometry, training, and previous experience with race time in 84 recreational, long-distance, inline skaters at the longest inline marathon in Europe (111 km), the Inline One-eleven in Switzerland, was investigated to identify predictor variables for performance. Age, duration per training unit, and personal best time were the only three variables related to race time in a multiple regression, while none of the 16 anthropometric variables were related. Anthropometric characteristics seem to be of no importance for a fast …

MaleGerontologyFuture studiesSWIMMING PERFORMANCEInline skating030204 cardiovascular system & hematologyRace (biology)0302 clinical medicineTRIATHLON PERFORMANCESMARATHON RUNNERSMENTAL TOUGHNESSPhysical Education and TrainingAnthropometrybiologyAge FactorsContrast (statistics)Middle AgedSensory SystemsTIMESkinfold Thickness[ SCCO.NEUR ] Cognitive science/Neurosciencesports.sport''SKIN-FOLD THICKNESSESPsychologyAdult11035 Institute of General PracticeBODY-COMPOSITIONsportsAccelerationExperimental and Cognitive Psychology610 Medicine & healthAthletic Performance03 medical and health sciences2809 Sensory SystemsHumansAssociation (psychology)ULTRA-MARATHONERSTIME''Athletes3205 Experimental and Cognitive Psychology[SCCO.NEUR]Cognitive science/NeuroscienceTraining (meteorology)030229 sport sciencesAnthropometrybiology.organism_classificationSKIN-FOLD THICKNESSESPractice PsychologicalSkatingPhysical EnduranceUPPER ARMRUNNING PERFORMANCE
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Developmental changes in the microgenesis of face perception revealed by effects of context and inversion

2011

AbstractPresent studies on the development of face perception mechanisms are ambiguous about the question of whether holistic face vision arises early, or in the second decade of life (Crookes & McKone, 2009). Measuring the time course of face matching we assess effects of context and inversion as correlates of holistic processing in the microgenesis of face perception within the first 650ms, and compare among 8- to 10-year-old children and adults. Results for adults indicate dominance of holistic viewing at brief timings, which is gradually replaced by feature selective strategies enabling them to selectively attend either internal or external features, as demanded by instruction. For chil…

MaleHolistic processingFace perceptionFace matchingFace inversion effect2809 Sensory SystemsChild DevelopmentDiscrimination PsychologicalFace perceptionHumansContextual informationChild10093 Institute of PsychologyInformation processingRecognition PsychologyInversion (meteorology)2731 OphthalmologySensory SystemsOphthalmologyFaceTime courseVisual PerceptionFemale150 PsychologyPsychologySocial psychologyInternal and external featuresCognitive psychologyVision Research
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Validity and reliability of an inertial sensor device for specific running patterns in soccer

2021

Electronic performance tracking devices are largely employed in team sports to monitor performance and improve training. To date, global positioning system (GPS) based devices are those mainly used in soccer training. The aim of this study was to analyse the validity and reliability of the inertial sensor device (ISD) in monitoring distance and speed in a soccer-specific circuit and how their performance compare to a GPS system. 44 young male soccer players (age: 14.9 ± 1.1, range 9–16, years, height: 1.65 ± 0.10 m, body mass: 56.3 ± 8.9 kg) playing in a non-professional soccer team in Italy, participated in the study. We assessed the players trough a soccer running sport-specific circuit. …

MaleInertial frame of referenceMean squared errorAdolescentGPSValidityTP1-1185Athletic PerformanceBiochemistryArticleAnalytical ChemistryInertial sensorRunningStatisticsSoccerRange (statistics)HumansElectrical and Electronic EngineeringChildInstrumentationMathematicsSettore M-EDF/02 - Metodi E Didattiche Delle Attivita' Sportivebusiness.industryChemical technologyReproducibility of ResultsTracking systemAtomic and Molecular Physics and OpticsAssisted GPSGlobal Positioning SystemGeographic Information SystemsData monitoringPerformance monitoringbusinessData trackingSettore M-EDF/01 - Metodi E Didattiche Delle Attivita' Motorie
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Giant axonal neuropathy and leukodystrophy

1991

Abstract An 11-year-old Persian boy, born to consanguineous parents, manifested a progressive gait abnormality beginning at 5 years of age. A severe cerebellar disorder developed with associated dysfunction of the peripheral nervous system, but no sign of mental impairment. The sensory and motor nerve conduction velocities were greatly reduced, especially in the lower extremities. Cerebrospinal fluid protein was normal. Computed tomography and magnetic resonance imaging revealed leukoencephalopathy, especially in the cerebellum, but also in periventricular areas. The diagnosis of giant axonal neuropathy was established by biopsy of the sural nerve. The few previous histologic examinations h…

MaleIntermediate FilamentsMotor nerveGenes RecessiveSural nerveCerebral VentriclesLeukoencephalopathyConsanguinityDevelopmental NeuroscienceCerebellummedicineHumansCerebellar disorderGliosisPeripheral NervesChildMyelin SheathSpinocerebellar DegenerationsGiant axonal neuropathybusiness.industryLeukodystrophyAnatomymedicine.diseaseMagnetic Resonance ImagingAxonsMicroscopy Electronmedicine.anatomical_structurenervous systemNeurologyPeripheral nervous systemPediatrics Perinatology and Child HealthGait abnormalityNeurology (clinical)medicine.symptomHereditary Sensory and Motor NeuropathybusinessPediatric Neurology
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Identification of three novel mutations in the MYO7A gene

1999

Three new mutations in the myosin VIIA gene involved in the pathogenesis of Usher syndrome type Ib are reported. These mutations are K1080X in exon 25, E1170K in exon 28, and Y1719C in exon 37. It is presumed that these mutations are involved in the Usher syndrome Ib phenotype. Hum Mutat 14:181, 1999. Copyright 1999 Wiley-Liss, Inc.

MaleMYO7AHearing Loss SensorineuralUsher syndromeMyosinsBiologymedicine.disease_causeExonRetinitis pigmentosaMyosinotorhinolaryngologic diseasesGeneticsmedicineHumansGenePolymorphism Single-Stranded ConformationalGenetics (clinical)GeneticsMutationBase SequenceChromosomes Human Pair 11fungiDyneinsSyndromemedicine.diseasePhenotypeeye diseasesPedigreePhenotypeMyosin VIIaMutationFemaleRetinitis PigmentosaHuman Mutation
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Comparison of three ultrasonic axial transmission methods for bone assessment.

2005

Abstract This study compared three approaches to bone assessment using ultrasonic axial transmission. In 41 fresh human radii, velocity of the first arriving signal was measured with a commercial device (Sunlight Omnisense ™ ) operating at 1.25 MHz, a prototype based on 1-MHz bidirectional axial transmission and a low-frequency (200 kHz) prototype, also measuring the velocity of a slower wave. Cortical and trabecular bone mineral density, cortical thickness and cross-sectional area were determined by peripheral quantitative computed tomography. Significant but modest correlation between velocities reflects differences in the nature of the propagating waves and methodological differences. Of…

MaleMaterials scienceAcoustics and UltrasonicsBiophysicsSignalBone and BonesBone DensitymedicineCadaverHumansRadiology Nuclear Medicine and imagingUltrasonicsQuantitative computed tomographyAxial transmissionAgedUltrasonographyAged 80 and overRadiological and Ultrasound Technologymedicine.diagnostic_testAnatomyMiddle AgedTrabecular boneRadiusmedicine.anatomical_structureMineral densityCortical boneUltrasonic sensorFemaleBiomedical engineeringUltrasound in medicinebiology
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<i>GJB2</i> Mutations and Genotype-Phenotype Correlation in 335 Patients from Germany with Nonsyndromic Sensorineural Hearing Loss: Evide…

2009

We report on 335 patients (319 families) with mild-to-profound nonsyndromic sensorineural hearing loss. We identified 178 mutated <i>GJB2</i> alleles representing 29 different sequence changes (including 3 novel mutations: Q7P, N14D, H100Q), and 2 alleles with the deletion del(GJB6-D13S1830) of the <i>GJB6</i> gene. Eleven <i>GJB2</i> mutations (119 mutated alleles) were truncating (T), and 18 mutations (59 alleles) were nontruncating (NT). Biallelic <i>GJB2</i> mutations were found in 71 patients (21.2%; 67 families; 25 different genotypes). Audiograms of 62 patients (56 families) with biallelic <i>GJB2</i> mutations typically ind…

MaleMild hearing impairmentPathologymedicine.medical_specialtyGenotypePhysiologyHearing lossHearing Loss SensorineuralGenes Recessivemedicine.disease_causePolymerase Chain ReactionConnexinsSpeech and HearingAudiometryGene FrequencyGermanyGenotypeotorhinolaryngologic diseasesmedicineHumansAlleleAllele frequencyAllelesGenetic Association StudiesGeneticsMutationbiologybusiness.industrymedicine.diseaseSensory SystemsConnexin 26PhenotypeOtorhinolaryngologyMutationbiology.proteinFemaleSensorineural hearing lossmedicine.symptombusinessGJB6Audiology and Neurotology
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