Search results for " Deaf"

showing 6 items of 36 documents

Cognition in Interaction : Challenges in Assessing Persons with Sensory and Multiple disabilities

2021

This article reports a qualitative study of cognitive assessments of three teenagers with sensory and multiple disabilities, including moderate to profound developmental disability. The aim was to evaluate the possibilities for adapting standardized tests and the implementation of interactional partnership in assessment. Cognitive assessments were made with an individually-adapted psychological assessment tool, the Bayley Scales of Infant and Toddler Development. The assessment situations were video-recorded and analyzed based on sociocultural theories of early interaction, dynamic assessment, and the bodily-tactile modality of cognition. The results showed that the requirements for assessm…

kognitiiviset taidotkognitiokuurosokeatvuorovaikutusarviointimenetelmätvammaisetaistivammaisetkognitiiviset prosessitcognitive assessmentsensory and multiple disabilitiescongenital deafblindnessdynamic assessmentagencykognitiivinen psykologiayksilöllisyysarviointikehitysvammaisetcompetent interactional partnership
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Beidseitige progrediente Hörminderung als Erstmanifestation eines metastasierenden Pankreaskopfkarzinoms - Kasuistik -

2001

We report the history of a patient who presented first with a progressive unilateral hearing loss and later with a bilateral deafness and an unilateral facial nerve palsy as first and only symptoms of a pancreatic adenocarcinoma. By means of magnetic resonance tomography tumor-suspect lesions in both internal auditory canals were detected. Referring to the results of further examinations these intracanalicular lesions are most probably due to rarely seen bilateral metastasis of a pancreatic adenocarcinoma in the temporal bone. In addition to this rarely diagnosed localisation of metastasis it is rather uncommon that this kind of primary malignoma had not been detected because of gastrointes…

medicine.medical_specialtybusiness.industryHearing lossBilateral Deafnessmedicine.diseaseFacial nerveFacial paralysisSurgeryMetastatic carcinomamedicine.anatomical_structureOtorhinolaryngologyInternal auditory meatusTemporal boneMedicinemedicine.symptomUnilateral hearing lossbusinessLaryngo-Rhino-Otologie
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Singing as a form of vocal imitation - Mechanisms and deficits

2009

There has been a recent upsurge of interest in the neural and cognitive bases of inaccurate singing, commonly referred to as “tone deafness.” Explanations of this deficit have commonly focused on perceptual and motor functions. It is clear, however, that neither of these mechanisms can fully account for deficits in singing. We summarize the results of several studies concerning inaccurate, or “poor pitch” singing. Taken together, the results of these studies argue that the basis for singing-related deficits lies in the link between perception and action, rather than strictly motoric or perceptual factors. Moreover, singing deficits may involve general purpose vocal imitation mechanisms, rat…

singingtone deafnessvocal imitationmusic performance
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I segni parlano. Prospettive di ricerca sulla Lingua dei Segni Italiana

2008

I segni parlano perché cominciano a farsi più visibili nella società italiana: le ricerche sulla Lingua dei Segni Italiana (LIS) – avviate in modo sistematico in Italia dagli inizi degli anni ‘80 – sono aumentate rispetto a diversi anni fa, così come è aumentata la consapevolezza dell’importanza di questa lingua, non solo per le persone sorde. È una lingua infatti che sempre più persone – familiari, amici e colleghi di persone sorde, operatori, insegnanti, studenti – desiderano apprendere ed utilizzare non solo per necessità ma per avvicinarsi a nuove modalità comunicative. Una lingua che purtroppo ancora oggi sente il peso del pregiudizio e fatica a liberarsi di quel senso di inferiorità r…

sorditàLingua dei Segni Struttura Comunità Sorda Sviluppo Linguistico lingue vocaliComunità SordaLingua dei Segni ItalianasordiStrutturaaccessibilitàSignwritingLISlingua dei segnilinguaggioSettore L-LIN/01 - Glottologia E LinguisticaaccessibilityIconicitàdeafnesssordità; cultura sorda; deaf studies; disability studies; lingua dei segni; linguaggio; deafness; deaf culture; sign language; accessibility; accessibilità; disabilità; sordi; LISdisability studiessign languagedeaf culturedisabilitàSviluppo Linguisticolingue vocalideaf studiescultura sordaLinguistica
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Lo spazio sociale della sordità: da individuo a comunità

2009

Lo studio analizza le caratteristiche della cmunità dei sordi in relazione alla maggioranza udente.

sorditàcomunità dei sordiinterpretariatosordiaccessibilitàLISlinguaggiolingua dei segniassistente alla comunicazioneComunità cultura sorda lingua dei segniSettore M-PED/04 - Pedagogia Sperimentaleaccessibilityeducazione dei sordideafnesssordità; cultura sorda; deaf studies; disability studies; lingua dei segni; linguaggio; deafness; deaf culture; sign language; accessibility; accessibilità; disabilità; sordi; LISdisability studiessign languagedeaf culturedisabilitàdeaf studiesComunitàcultura sorda
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Variants of human CLDN9 cause mild to profound hearing loss

2021

Hereditary deafness is clinically and genetically heterogeneous. We investigated deafness segregating as a recessive trait in two families. Audiological examinations revealed an asymmetric mild to profound hearing loss with childhood or adolescent onset. Exome sequencing of probands identified a homozygous c.475G>A;p.(Glu159Lys) variant of CLDN9 (NM_020982.4) in one family and a homozygous c.370_372dupATC;p.(Ile124dup) CLDN9 variant in an affected individual of a second family. Claudin 9 (CLDN9) is an integral membrane protein and constituent of epithelial bicellular tight junctions that form semi-permeable, paracellular barriers between inner ear perilymphatic and endolymphatic compartment…

tight junctionsAdolescentclaudin 9In situ hybridizationDeafnessBiologyArticleFrameshift mutationMiceotorhinolaryngologic diseasesGeneticsmedicineAnimalsHumansPakistanInner earNonsyndromic deafnessChildClaudinGenetics (clinical)Exome sequencingnonsyndromic deafnessTight junctionGenetic heterogeneityclaudin 9; exome sequencing; Morocco; nonsyndromic deafness; Pakistan; tight junctionsHomozygotemedicine.diseaseMolecular biologyPedigreeMoroccomedicine.anatomical_structureClaudinsMutationexome sequencingHeLa CellsHuman Mutation
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