Search results for "Kind"
showing 10 items of 173 documents
No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder.
2008
Contains fulltext : 71091.pdf (Publisher’s version ) (Closed access) Several independent studies have reported association between serotonin transporter gene (SLC6A4) polymorphisms and attention deficit hyperactivity disorder (ADHD). Five studies found evidence for association between the long-allele of a 44-bp insertion/deletion polymorphism (5-HTTLPR) and ADHD. Another two studies corroborated this finding while a further six studies did not find such an association. For a second polymorphism within the gene, a variable number tandem repeat (VNTR) within intron 2, one study demonstrated that the 12/12 genotype was significantly less frequent in ADHD cases compared to controls, while a sec…
Génèse et évolution des compétences des élèves à la fin de l'école maternelle : éléments d'analyse à partir de données de panel et d'une expérimentat…
2012
We propose to study in this thesis, a key issue and relatively little discussed in the French research in educational sciences, it concerns the genesis of pupil learning and their evolution during the tuition. We mobilize a longitudinal data (Panel 1997) and the results of a musical experimentation in kindergarten to answer to these questions: How are structured the first acquisitions of pupils and how is it linked to the school context and socio-economic variables? How the cognitive abilities of students affect their academic performance? Are specific activities can improve academic skills through an increase in cognitive abilities? Implicative analysis conducted on panel data has revealed…
Gemurmel und Gebrabbel : Probleme beim Übersetzen von Patrick Süskinds Der Zwang zur Tiefe
2018
Sekä kirjallinen että suullinen kääntäminen on kuulunut ihmisten elämään jo vuosituhansien ajan, ja usein oletetaan, ettei kääntäminen ole kielitaitoiselle ihmiselle haasteellista. Tässä kandidaatintutkielmassa haluttiin tuoda esille käännöstieteen monimutkaisuutta, sekä erityisesti itse kääntämisen ongelmakohtia. Tutkielmaa varten käännettiin Patrick Süskindin novelli Der Zwang zur Tiefe saksasta suomeksi, ja tavoitteena oli esitellä, millaisia ongelmia kääntämisessä ilmeni, ja kuinka näitä ongelmia pyrittiin selvittämään. Käännöstyön aikana ilmenneet moninaiset ongelmat jaoteltiin kuuteen kategoriaan. Käsiteltäviä ongelmia olivat novellin nimen kääntäminen, pronominit, sanasto, onomatopoe…
Projekts: Privātā bērnudārza "Saulīte" dibināšana
2020
Tuvākajā laikā tiks izveidots uzņēmums „Saulīte S”, un tā pamatdarbība ir plānota bērnudārzu pakalpojumu sniegšana pirmsskolas vecuma bērniem. Atrašanas vieta: Mārupe, īpašnieks: Romāns Moskaļovs, pamatkapitāls: 5000 EUR, uzņēmuma darbības nozare: Pirmskolas izglītība (NACE klasifikators P85.10, versija 2.0) (Avots: VID, CSP, ZO.LV). Uzņēmējdarbības mērķi ir nodrošināt drošu un veselībai nekaitīgu bērnu aprūpi, kā arī agrīnu (1 līdz 3 gadu vecu) bērnu attīstību un sagatavošanos viņu pirmajai skolai, izmantojot jaunākās procedūras un paņēmienus šo mērķu sasniegšanai. Telpas uzņēmuma “Saulīte S” bērnudārza komercdarbībai tiks izīrētas uz ilgtermiņa 5 gadu līguma pamata, nomas maksa būs 780 EU…
Estudio del perfil oxidativo en el síndrome de Kindler
2014
El Síndrome de Kindler (SK) es una rara genodermatosis cuyas manifestaciones principales son atrofia y envejecimiento prematuro de la piel, fotosensibilidad y carcinoma de piel, síntomas que comparte con otros síndromes (p. ej. Síndrome de Werner) en los que se ha demostrado la implicación del estrés oxidativo; sin embargo, en el SK no ha sido estudiado previamente. En el SK se ha identificado una alteración del brazo corto del cromosoma 20, donde se encuentra el gen KIND-1 que codifica la proteína kindlina-1. La pérdida de función de este gen conduce a una disminución de la síntesis de la proteína kindlina-1, produciendo, a su vez, una reducción de la adhesión de la interfase dermis-epider…
Zaniedbane emocjonalnie dzieci – symptomy, diagnoza, formy wsparcia w środowisku przedszkolnym
2020
This article aims to present analysis of possible actions of kindergarten teachers and other specialists working with emotionally neglected children. The first part of the text includes definition of emotional neglect and information about the symptoms observed in emotionally neglected child. The short term and long term consequences of emotional neglect in group of children aged 3–6 were shortly described. The characteristics enabling recognition of emotional neglect and diagnostic procedures facilitating identification of a problem by teachers and kindergarten specialists were given. Basic cues concerning the work with emotionally neglected child that can be accomplished in kindergarten, …
Gender and Work-life balance: a contest analysis on nursey schools in Palermo
2018
This paper reflects on the gender inequalities and their influence in the access to labor market and, on the other one, to reproductive process. Maternity and work often arise as choices excluding one another due for the inadequacy of care services. The essay reviews some laws of the last years for encourage the work-life balance and analyzes the presence of the services for children in Palermo. The "case study" of the municipality of Palermo shows a general lack of services and a progressive reduction of public nurseries and kindergarten, despite the economic investments of the last decades at institutional level. It points out how many obstacles persist that discourage female participatio…
Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.
2008
Contains fulltext : 70149.pdf (Publisher’s version ) (Closed access) A time-to-onset analysis for family-based samples was performed on the genomewide association (GWAS) data for attention deficit hyperactivity disorder (ADHD) to determine if associations exist with the age at onset of ADHD. The initial dataset consisted of 958 parent-offspring trios that were genotyped on the Perlegen 600,000 SNP array. After data cleaning procedures, 429,981 autosomal SNPs and 930 parent-offspring trios were used found suitable for use and a family-based logrank analysis was performed using that age at first ADHD symptoms as the quantitative trait of interest. No SNP achieved genome-wide significance, and…
Dopamine and serotonin transporter genotypes moderate sensitivity to maternal expressed emotion: the case of conduct and emotional problems in attent…
2009
Contains fulltext : 80906.pdf (Publisher’s version ) (Closed access) BACKGROUND: Mothers' positive emotions expressed about their children with attention deficit/hyperactivity disorder (ADHD) are associated with a reduced likelihood of comorbid conduct problems (CP). We examined whether this association with CP, and one with emotional problems (EMO), is moderated by variants within three genes, previously reported to be associated with ADHD and to moderate the impact of environmental risks on conduct and/or emotional problems; the dopamine transporter gene (SLC6A3/DAT1), the dopamine D4 receptor gene (DRD4) and the serotonin transporter gene (SLC6A4/5HTT). METHODS: Seven hundred and twenty-…
Motor differentiation's and cognitive skill in pre-scholar age
2019
ABSTRACT Little research has been produced about literacy readiness in Kindergarten children at risk for Developmental Coordination Disorder (DCD), despite this age being one of the most important epoch of motor and cognitive development. In this study we compared pre-literacy skills in Kindergarten children at risk for Developmental Coordination Disorder (DCD) with Typically Developing (TD) children. Participants were 26 Italian children, who had a mean age of 5.1 years, 13 at risk for DCD and 13 TD attending kindergarten schools. Pre-literacy abilities were measured trough tasks derived by the Italian PRCR-2 battery: Semi-circles (A and B), Letter identification and Object Naming Time. Ch…