635 research outputs found

    Les collections de littérature jeunesse à contenu LGBTQ dans les bibliothèques publiques québécoises : portrait et évaluation

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    Cette étude dresse le portrait des collections de littérature jeunesse à contenu LGBTQ dans les bibliothèques publiques québécoises afin de déterminer si la population est bien servie à cet égard, peu importe le lieu et la taille de la collectivité. Pour ce faire, nous avons adopté une approche qualitative et utilisé la méthode de l’évaluation par liste. Ainsi, les collections de 41 bibliothèques publiques municipales ont été examinées au moyen d’une liste de vérification de 38 titres de littérature jeunesse à contenu LGBTQ publiés de 2003 à 2018. Les données recueillies ont fait l’objet d’une analyse statistique surtout descriptive. À l’instar d’études antérieures sur les collections des bibliothèques canadiennes et américaines, la présente recherche a montré que le niveau de présence de la littérature jeunesse à contenu LGBTQ varie considérablement selon les bibliothèques et que la taille des populations, l’importance des collections et le budget consacré aux livres ne suffisent pas à expliquer toutes les fluctuations. L’analyse des données a aussi permis de révéler que les romans à contenu LGBTQ destinés aux ados étaient beaucoup plus susceptibles de figurer dans les collections que les albums et les premiers romans destinés aux enfants. De plus, l’analyse a montré que le thème de l’homosexualité masculine était largement représenté dans les collections, tandis que celui de l’homoparentalité était considérablement sous-représenté. Pourtant, selon les données recueillies, les albums pour enfants sur le thème de l’homoparentalité sont justement le type de matériel qui était le plus emprunté dans les bibliothèques au moment de l’étude. Cette étude exploratoire ne permet pas de conclure avec certitude que les collections de littérature jeunesse à contenu LGBTQ dans les bibliothèques québécoises sont suffisantes et appropriées. Toutefois, la comparaison des résultats obtenus avec ceux d’autres recherches suggère que, dans l’ensemble, les bibliothèques québécoises font plutôt bien à cet égard.The purpose of this study is to examine the stocks of young adult and children’s literature collections with LGBTQ content made available in Québec public libraries to determine whether the population is sufficiently provided for, regardless of the location and size of the city or town where they live. To carry out this research project, we used the checklist evaluation method. Collections from a sample of 41 municipal public libraries were thus examined, using a checklist of 38 young adult and children’s literature titles with LGBTQ content, published from 2003 to 2018. The collected data was subjected to statistical analysis. As with previous studies of Canadian and American public library collections, this research has shown that the level of presence of young adult and children’s literature with LGBTQ content varies considerably in all libraries, and that the size of populations, the size of collections and the budgets for printed books can’t explain all the fluctuations. Data analysis also revealed that novels with LGBTQ content for teenagers were much more likely to be held in collections than early readers’ novels and children’s picture books. The results have also shown that male homosexuality as a theme is well represented in the collections, while same sex parenthood is significantly underrepresented. However, according to the data, the picture books for children on the topic of same-sex parenthood are exactly the type of material which was the most borrowed in the sampled libraries at the time of the study. This exploratory study alone does not entirely support the conclusion that collections of young adult and children’s literature with LGBTQ content in Québec public libraries are sufficient and appropriate. However, comparing results from this research to those from other researches suggests that, overall, Quebec libraries seem to be doing well in this regard

    Conscience morphologique et habiletés d'orthographe chez les enfants du premier cycle du primaire ayant des difficultés en langage écrit : une étude d'intervention

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    Quel enfant ne s’est jamais cassé la tête sur la finale muette d’un mot? La morphologie et les accords grammaticaux qu’elle implique sont encodés dans une multitude de mots du français et constituent un des grands défis de l’apprentissage de l’orthographe. Elle s’avère d’autant plus complexe et obscure pour les élèves ayant des difficultés à manipuler la structure des mots, c’est à dire ayant de faibles habiletés de conscience morphologique. Afin d’aider ces enfants, cette recherche s’intéresse à l’intervention sur cette habileté langagière comme facilitateur de l’apprentissage de l’orthographe. Une intervention professionnelle a été élaborée et offerte à des enfants québécois de 2e année du 1er cycle ayant des difficultés en langage écrit. Celle-ci s’est avérée efficace, c’est-à-dire qu’elle a mené à une amélioration significative et durable des compétences en orthographe des élèves ciblés. La conscience morphologique pouvant aussi être intégrée dans l’enseignement de l’orthographe en classe, une formation ponctuelle a été développée, toujours dans le cadre de cette recherche, et son actualisation s’est faite via l’infrastructure sociotechnique de l’École éloignée en réseau. Cette formation a mené à une prise de conscience des enseignants quant au recours à des connaissances en morphologie dans leurs pratiques quotidiennes pour l’enseignement de l’orthographe. À la lumière des résultats obtenus, il importe de développer et mettre en place des interventions ciblées sur la morphologie et ses relations avec l’écriture des mots pour le développement optimal des habiletés d’orthographe des enfants tout-venant et en difficulté. Celles-ci peuvent s’inscrire tant dans l’action professionnelle d’intervenants spécialisés que dans un enseignement en salle de classe, et ce, dès la 2e année du 1er cycle

    Communauté de pratique, technologie et réponse à l'intervention en compréhension de lecture pour le développement de pratiques enseignantes soutenant les habiletés langagières réceptives chez les enfants de milieux défavorisés

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    Dès le 2e cycle, les élèves relèvent divers défis en compréhension de lecture (CL) dont la réussite repose sur leurs habiletés langagières. Pour ce faire, les enseignants ont un rôle incontournable à jouer pour les amener à devenir des lecteurs stratégiques qui comprennent bien ce qu’ils lisent. Ce rôle est d’autant plus important pour les élèves issus de milieux défavorisés qui sont fortement à risque de présenter des difficultés langagières. Toutefois, les enseignants se sentent peu outillés pour favoriser le développement de la CL chez ces enfants. La communauté de pratique (CoP) ÉCRIT a été développée et mise en place sur la plateforme Web d’École en Réseau (ÉER). Elle a mené des enseignantes du primaire œuvrant auprès d’une clientèle défavorisée à comprendre et à appliquer nombre de notions sur le langage et son rôle dans la CL, en termes de connaissances, stratégies d’enseignement et comportements à adopter. Prises de conscience, initiatives pédagogiques et intégration de nouvelles pratiques pédagogiques en classe ont été au rendez-vous. Selon le regard des enseignants, une modification des pratiques qui inclue un soutien plus explicite des habiletés langagières a des répercussions positives sur la réussite scolaire des élèves, leur motivation et leur participation. Ainsi, l’instauration d’une CoP orientée sur les habiletés langagières et la CL s’avère un levier puissant pour outiller les enseignants dans leurs enseignements auprès des élèves et ainsi soutenir le développement de pratiques pédagogiques reconnues optimales par la recherche. Dans le cadre d’une approche Réponse à l’Intervention, telle que préconisée par le MEES, ce moyen permet de contribuer à l’amélioration continue de la qualité de l’enseignement en salle de classe (palier 1)

    Long-acting injectable Cabotegravir + Rilpivirine for HIV maintenance therapy: Week 48 pooled analysis of phase 3 ATLAS and FLAIR trials

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    BACKGROUND: Long-acting (LA) injectable regimens are a potential therapeutic option in people living with HIV-1. SETTING: ATLAS (NCT02951052) and FLAIR (NCT02938520) were 2 randomized, open-label, multicenter, multinational phase 3 studies. METHODS: Adult participants with virologic suppression (plasma HIV-1 RNA <50 copies/mL) were randomized (1:1) to continue with their current antiretroviral regimen (CAR) or switch to the long-acting (LA) regimen of cabotegravir (CAB) and rilpivirine (RPV). In the LA arm, participants initially received oral CAB + RPV once-daily for 4 weeks to assess individual safety and tolerability, before starting monthly injectable therapy. The primary endpoint of this combined analysis was antiviral efficacy at week 48 (FDA Snapshot algorithm: noninferiority margin of 4% for HIV-1 RNA ≥50 copies/mL). Safety, tolerability, and confirmed virologic failure (2 consecutive plasma HIV-1 RNA ≥200 copies/mL) were secondary endpoints. RESULTS: The pooled intention-to-treat exposed population included 591 participants in each arm [28% women (sex at birth), 19% aged ≥50 years]. Noninferiority criteria at week 48 were met for the primary (HIV-1 RNA ≥50 copies/mL) and key secondary (HIV-1 RNA <50 copies/mL) efficacy endpoints. Seven individuals in each arm (1.2%) developed confirmed virologic failure; 6/7 (LA) and 3/7 (CAR) had resistance-associated mutations. Most LA recipients (83%) experienced injection site reactions, which decreased in incidence over time. Injection site reactions led to the withdrawal of 6 (1%) participants. The serious adverse event rate was 4% in each arm. CONCLUSION: This combined analysis demonstrates monthly injections of CAB + RPV LA were noninferior to daily oral CAR for maintaining HIV-1 suppression

    Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: towards recommendation for molecular testing and management

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    International audienceSHORT syndrome has historically been defined by its acronym: short stature (S), hyperextensibility of joints and/or inguinal hernia (H), ocular depression (O), Rieger abnormality (R) and teething delay (T). More recently several research groups have identified PIK3R1 mutations as responsible for SHORT syndrome. Knowledge of the molecular etiology of SHORT syndrome has permitted a reassessment of the clinical phenotype. The detailed phenotypes of 32 individuals with SHORT syndrome and PIK3R1 mutation, including eight newly ascertained individuals, were studied to fully define the syndrome and the indications for PIK3R1 testing. The major features described in the SHORT acronym were not universally seen and only half (52%) had 4 or more of the classic features. The commonly observed clinical features of SHORT syndrome seen in the cohort included IUGR \textless 10(th) percentile, postnatal growth restriction, lipoatrophy and the characteristic facial gestalt. Anterior chamber defects and insulin resistance or diabetes were also observed but were not as prevalent. The less specific, or minor features of SHORT syndrome include teething delay, thin wrinkled skin, speech delay, sensorineural deafness, hyperextensibility of joints and inguinal hernia. Given the high risk of diabetes mellitus, regular monitoring of glucose metabolism is warranted. An echocardiogram, ophthalmological and hearing assessments are also recommended

    Genetic diversity, linkage disequilibrium and power of a large grapevine (Vitis vinifera L) diversity panel newly designed for association studies

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    UMR-AGAP Equipe DAVV (Diversité, adaptation et amélioration de la vigne) ; équipe ID (Intégration de Données)International audienceAbstractBackgroundAs for many crops, new high-quality grapevine varieties requiring less pesticide and adapted to climate change are needed. In perennial species, breeding is a long process which can be speeded up by gaining knowledge about quantitative trait loci linked to agronomic traits variation. However, due to the long juvenile period of these species, establishing numerous highly recombinant populations for high resolution mapping is both costly and time-consuming. Genome wide association studies in germplasm panels is an alternative method of choice, since it allows identifying the main quantitative trait loci with high resolution by exploiting past recombination events between cultivars. Such studies require adequate panel design to represent most of the available genetic and phenotypic diversity. Assessing linkage disequilibrium extent and panel power is also needed to determine the marker density required for association studies.ResultsStarting from the largest grapevine collection worldwide maintained in Vassal (France), we designed a diversity panel of 279 cultivars with limited relatedness, reflecting the low structuration in three genetic pools resulting from different uses (table vs wine) and geographical origin (East vs West), and including the major founders of modern cultivars. With 20 simple sequence repeat markers and five quantitative traits, we showed that our panel adequately captured most of the genetic and phenotypic diversity existing within the entire Vassal collection. To assess linkage disequilibrium extent and panel power, we genotyped single nucleotide polymorphisms: 372 over four genomic regions and 129 distributed over the whole genome. Linkage disequilibrium, measured by correlation corrected for kinship, reached 0.2 for a physical distance between 9 and 458 Kb depending on genetic pool and genomic region, with varying size of linkage disequilibrium blocks. This panel achieved reasonable power to detect associations between traits with high broad-sense heritability (> 0.7) and causal loci with intermediate allelic frequency and strong effect (explaining > 10 % of total variance).ConclusionsOur association panel constitutes a new, highly valuable resource for genetic association studies in grapevine, and deserves dissemination to diverse field and greenhouse trials to gain more insight into the genetic control of many agronomic traits and their interaction with the environment

    DMTs and Covid-19 severity in MS: a pooled analysis from Italy and France

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    We evaluated the effect of DMTs on Covid-19 severity in patients with MS, with a pooled-analysis of two large cohorts from Italy and France. The association of baseline characteristics and DMTs with Covid-19 severity was assessed by multivariate ordinal-logistic models and pooled by a fixed-effect meta-analysis. 1066 patients with MS from Italy and 721 from France were included. In the multivariate model, anti-CD20 therapies were significantly associated (OR = 2.05, 95%CI = 1.39–3.02, p < 0.001) with Covid-19 severity, whereas interferon indicated a decreased risk (OR = 0.42, 95%CI = 0.18–0.99, p = 0.047). This pooled-analysis confirms an increased risk of severe Covid-19 in patients on anti-CD20 therapies and supports the protective role of interferon

    Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

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    Publisher Copyright: © 2021 The Authors, some rights reserved.Circulating autoantibodies (auto-Abs) neutralizing high concentrations (10 ng/ml; in plasma diluted 1:10) of IFN-alpha and/or IFN-omega are found in about 10% of patients with critical COVID-19 (coronavirus disease 2019) pneumonia but not in individuals with asymptomatic infections. We detect auto-Abs neutralizing 100-fold lower, more physiological, concentrations of IFN-alpha and/or IFN-omega (100 pg/ml; in 1:10 dilutions of plasma) in 13.6% of 3595 patients with critical COVID-19, including 21% of 374 patients >80 years, and 6.5% of 522 patients with severe COVID-19. These antibodies are also detected in 18% of the 1124 deceased patients (aged 20 days to 99 years; mean: 70 years). Moreover, another 1.3% of patients with critical COVID-19 and 0.9% of the deceased patients have auto-Abs neutralizing high concentrations of IFN-beta. We also show, in a sample of 34,159 uninfected individuals from the general population, that auto-Abs neutralizing high concentrations of IFN-alpha and/or IFN-omega are present in 0.18% of individuals between 18 and 69 years, 1.1% between 70 and 79 years, and 3.4% >80 years. Moreover, the proportion of individuals carrying auto-Abs neutralizing lower concentrations is greater in a subsample of 10,778 uninfected individuals: 1% of individuals 80 years. By contrast, auto-Abs neutralizing IFN-beta do not become more frequent with age. Auto-Abs neutralizing type I IFNs predate SARS-CoV-2 infection and sharply increase in prevalence after the age of 70 years. They account for about 20% of both critical COVID-19 cases in the over 80s and total fatal COVID-19 cases.Peer reviewe

    Identification of common genetic risk variants for autism spectrum disorder

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    Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of neurodevelopmental phenotypes diagnosed in more than 1% of children. Common genetic variants contribute substantially to ASD susceptibility, but to date no individual variants have been robustly associated with ASD. With a marked sample-size increase from a unique Danish population resource, we report a genome-wide association meta-analysis of 18,381 individuals with ASD and 27,969 controls that identified five genome-wide-significant loci. Leveraging GWAS results from three phenotypes with significantly overlapping genetic architectures (schizophrenia, major depression, and educational attainment), we identified seven additional loci shared with other traits at equally strict significance levels. Dissecting the polygenic architecture, we found both quantitative and qualitative polygenic heterogeneity across ASD subtypes. These results highlight biological insights, particularly relating to neuronal function and corticogenesis, and establish that GWAS performed at scale will be much more productive in the near term in ASD

    Penilaian Kinerja Keuangan Koperasi di Kabupaten Pelalawan

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    This paper describe development and financial performance of cooperative in District Pelalawan among 2007 - 2008. Studies on primary and secondary cooperative in 12 sub-districts. Method in this stady use performance measuring of productivity, efficiency, growth, liquidity, and solvability of cooperative. Productivity of cooperative in Pelalawan was highly but efficiency still low. Profit and income were highly, even liquidity of cooperative very high, and solvability was good
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