Search results for "disability"

showing 10 items of 989 documents

MEMORIA DE TRABAJO EN NIÑOS DE EDUCACIÓN INFANTIL CON Y SIN BAJO RENDIMIENTO MATEMÁTICO

2014

Abstract:This study aims to explore working memory in preschool children with and without low mathematical performance. The sample consisted of 255 children aged 5-6 years, to whom were administered neuropsychological tests of working memory and TEDI-MATH to estimate the mathematical performance. The results highlight the capacity of verbal working memory to significantly differentiate groups of children with and without problems in 8 of the 9 analyzed mathematical domains. This factor together with visuospatial working memory differentiate the group of children at risk for mathematical learning disabilities.Keywords: working memory, preschool, math performance, mathematics learning disabil…

Working memorylcsh:BF1-99005 social sciences050301 educationDevelopmental psychologyeducación infantillcsh:Psychologyrendimiento matemáticodificultades de aprendizaje de las matemáticasLearning disabilitymedicinememoria de trabajo0501 psychology and cognitive sciencesmedicine.symptomPsychology0503 education050104 developmental & child psychologyInternational Journal of Developmental and Educational Psychology. Revista INFAD de Psicología.
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Age-dependent epileptic encephalopathy associated with an unusual co-occurrence of ZEB2 and SCN1A variants.

2020

Mowat-Wilson syndrome is a genetic disorder associated with a variable phenotype including peculiar facial features associated with intellectual disability, epilepsy, language impairment, and multiple congenital anomalies caused by heterozygous mutation of the ZEB2 gene. The ZEB2 protein is a complex transcription factor that encompasses multiple functional domains that interact with the regulatory regions of target genes including those involved in brain development. Recently, it has been documented that ZEB2 regulates the differentiation of interneuron progenitors migrating from the medial ganglionic eminence to cortical layers by repression of the Nkx2-1 homeobox transcription factor. It…

ZEB2genotype-phenotype correlationSettore MED/38 - Pediatria Generale E SpecialisticaSettore M-PSI/08 - Psicologia ClinicaIntellectual DisabilityHumansMowat-Wilson syndromeEEGgenotype-phenotype correlationSCN1AHirschsprung DiseaseEEGChildGenetic Association StudiesZEB2Zinc Finger E-box Binding Homeobox 2EpilepsyEEG; epilepsy; GABAergic interneurons; genotype-phenotype correlation; Mowat-Wilson syndrome; SCN1A; ZEB2FaciesElectroencephalographySettore MED/39 - Neuropsichiatria InfantileGABAergic interneuronsMowat-Wilson syndromeepilepsyNAV1.1 Voltage-Gated Sodium ChannelGABAergic interneuronsMicrocephalySettore MED/26 - NeurologiaFemaleEpileptic disorders : international epilepsy journal with videotape
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Kehitysvammaisten aikuisten kestävyyskunnon taso ja muutos ikääntyessä : kahden kävelytestin vertaaminen

2015

Eveliina Keinonen (2015). Kehitysvammaisten aikuisten kestävyyskunnon taso ja muutos ikääntyessä: Kahden kävelytestin vertaaminen. Liikuntakasvatuksen laitos, Jyväskylän yli-opisto, liikuntapedagogiikan pro gradu –tutkielma, 66 s., 3 liitettä. Tutkimuksen tavoitteena oli tarkastella keski-ikäisten kehitysvammaisten naisten ja miesten kestävyyskunnon tasoa vammattomaan väestöön sekä Suomessa yleisesti käytössä oleviin terveysliikunnan suosituksiin verrattuna. Tarkastelun kohteena oli myös kehitysvammaisten kestävyyskunnossa esiintyvät muutokset seitsemän vuoden aikana. Lisäksi tutkimus pyrki selvittämään onko samanaikaisesti suoritettujen UKK-instituutin 2 kilometrin kävelytestin ja Rockport…

aerobic capacitycardiovascular fitness testingkehitysvammaisuusfyysinen kuntokestävyyskunnon mittaaminenkestävyyskuntointellectual disabilitykuntotestitkehitysvammaiset
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Diagnostic therapeutic flow-charts for low-back pain patient : the Italian clinical guidelines

2006

antidepressant agentmuscle relaxant agentnonsteroid antiinflammatory agentparacetamol addictiondiagnostic proceduredrowsinessexercisehumanhyperthermic therapyItalylow back painmassagepractice guidelinereview Disability EvaluationHumansItalyLow Back Pain
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Edukacyjny wymiar pracy nad własną biografią

2017

The biographical approach is gaining more and more recognition among educators who have found an effective way to work with adults. The article describes the place of narration in pedagogy and adult education. Working on your own biography isn’t just a summary of your life, but a reflection on the present and future. It what characterizes this method is the subject matter of research and reflection, which is the life of a particular individual, included in a written or spoken narration. For this reason, this method has educational value because it allows the individual to constructive reflection on her own life, while on the other hand she is a valuable source of information for the pedagog…

biographical narrativedisabilitybiographical methodadult education
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Accesible co-creation tools for people with intellectual disabilities: working for and with end-users

2019

In a world defined by rapid change, the search for solutions to societal challenges has become more complex calling for new paradigms of innovation focused on collaborations with the community and users. Co-creation approaches in the design and production of a service or product can bring low-cost innovation and unique and personalized customer experiences leading to user acceptance of a product or service. Under a co-creation perspective, the participatory approach developed in the MINDInclusion project aims to improve the inclusion of people with intellectual disabilities into public places and society by using a co-created online tool based on people with disabilities’ personal experienc…

business.industryEnd userCo-creationInternet privacyIntellectual disabilityDocumentationmedicine.diseaseDocumentationCognitive accessibilityIntellectual disabilitymedicineCo-creationSociologybusinessInnovationTeaching TechnologiesSocial inclusion
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BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

2021

AbstractPurposeHeterozygous variants in BCL11A underlie an intellectual developmental disorder with persistence of fetal hemoglobin (BCL11A-IDD, a.k.a. Dias-Logan syndrome). We sought to delineate the genotypic and phenotypic spectrum of BCL11A-IDD.MethodsWe performed an in-depth analysis of 42 patients with BCL11A-IDD ascertained through a collaborative network of clinical and research colleagues. We also reviewed 33 additional affected individuals previously reported in the literature or available through public repositories with clinical information.ResultsMolecular and clinical data analysis of 75 patients with BCL11A-IDD identified 60 unique variants (30 frameshift, 7 missense, 6 splic…

business.industryPostnatal microcephalyMicrodeletion syndromemedicine.diseaseBioinformaticsHypotoniaDevelopmental disorderAutism spectrum disorderIntellectual disabilityFetal hemoglobinmedicineMissense mutationmedicine.symptombusiness
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Intervención psicológica en natación adaptada desde la perspectiva del coaching motivacional

2016

Este artículo presenta la intervención psicológica realizada con una mujer deportista de 19 años que presenta una discapacidad física y cuyo objetivo principal es el de acabar una travesía a nado en mar abierto. Para ayudarla en el logro de su meta, se realizan siete sesiones con una frecuencia de una vez a la semana tomando como punto de partida el modelo de coaching motivacional “La Jirafa de Cantón”, donde el psicólogo genera un entorno facilitador para que el cliente descubra y encuentre sus propias soluciones. En cuanto a la evaluación de su eficacia, se utiliza un diseño test-retest con los siguientes instrumentos: “Escala de Autoestima” de Rosenberg (1965), “Escala de Bienestar Psico…

business.industrymedia_common.quotation_subjectPsychological interventionNatacióCoachingA physical disabilityOpen seaPerceptionIntrinsic motivationPsychologybusinessCartographySocial psychologyMotivació (Psicologia)media_commonINFORMACIÓ PSICOLÒGICA
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Care for People with Disabilities in Italy: A Critical Analysis of Act 112/2016 on Assistance for People with Serious Disabilities Lacking Family Sup…

2019

The paper focuses on the issue of care assistance for people with disabilities in Italy, examining the recent Act n. 112 adopted by the Italian Parliament in June 2016 and entitled “Measures in the field of assistance for people with serious disabilities lacking family support” (Disposizioni in materia di assistenza in favore delle persone con disabilità grave prive del sostegno familiare). In particular, I explore whether and how this legislative intervention effectively meets the needs of people with disabilities, especially with regard to their right to live independently and be included in the community as provided by Article 19 of the 2006 UN Convention on the Rights of Persons with Di…

careSettore IUS/02 - Diritto Privato ComparatoSettore SPS/12 - Sociologia Giuridica della Devianza e Mutamento Socialepeople with disabilitywelfare state
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Sytuacja prawna dziecka niepełnosprawnego w rodzinie dysfunkcyjnej

2019

childfamilydysfunctionniepełnosprawnośćneglectdzieckofamily supportprzemocviolencedisabilityzaniedbaniedysfunkcjawsparcie rodzinyrodzina
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