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Dislexia
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1121“…Government/aided teachers had better general knowledge regarding LDs and dyslexia than private teachers. CONCLUSIONS: Among 80 teachers, 70% (56) of them had adequate general knowledge regarding LDs. …”
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1122por Montgomery, Paul, Burton, Jennifer R., Sewell, Richard P., Spreckelsen, Thees F., Richardson, Alexandra J.“…These findings require confirmation, but suggest that the benefits from dietary supplementation with Omega-3 LC-PUFA found for ADHD, Dyspraxia, Dyslexia, and related conditions might extend to the general school population.…”
Publicado 2013
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1123por St Pourcain, Beate, Cents, Rolieke A.M., Whitehouse, Andrew J.O., Haworth, Claire M.A., Davis, Oliver S.P., O’Reilly, Paul F., Roulstone, Susan, Wren, Yvonne, Ang, Qi W., Velders, Fleur P., Evans, David M., Kemp, John P., Warrington, Nicole M., Miller, Laura, Timpson, Nicholas J., Ring, Susan M., Verhulst, Frank C., Hofman, Albert, Rivadeneira, Fernando, Meaburn, Emma L., Price, Thomas S., Dale, Philip S., Pillas, Demetris, Yliherva, Anneli, Rodriguez, Alina, Golding, Jean, Jaddoe, Vincent W.V., Jarvelin, Marjo-Riitta, Plomin, Robert, Pennell, Craig E., Tiemeier, Henning, Davey Smith, George“…This association links language-related common genetic variation in the general population to a potential autism susceptibility locus and a linkage region for dyslexia, speech-sound disorder and reading. The contribution of common genetic influences is, although modest, supported by genome-wide complex trait analysis (meta-GCTA h(2)(15–18-months)=0.13, meta-GCTA h(2)(24–30-months)=0.14) and in concordance with additional twin analysis (5,733 pairs of European descent, h(2)(24-months)=0.20).…”
Publicado 2014
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1124“…They commonly described longstanding non-autistic neurodevelopmental problems, including dyslexia, dyspraxia and epilepsy. Only one had a childhood diagnosis of ASD. …”
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1125por Pettigrew, Kerry A., Frinton, Emily, Nudel, Ron, Chan, May T. M., Thompson, Paul, Hayiou-Thomas, Marianna E., Talcott, Joel B., Stein, John, Monaco, Anthony P., Hulme, Charles, Snowling, Margaret J., Newbury, Dianne F., Paracchini, Silvia“…METHODS: We used two independent family-based cohorts characterised with reading- and language-related traits: a longitudinal cohort (n = 106 informative families) including children with language and reading difficulties and a nuclear family cohort (n = 264 families) selected for dyslexia. RESULTS: We observed association with language-related measures when modelling for parent-of-origin effects at the NOP9 locus in both cohorts: minimum P = 0.001 for phonological awareness with a paternal effect in the first cohort and minimum P = 0.0004 for irregular word reading with a maternal effect in the second cohort. …”
Publicado 2016
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1126por Woollams, Anna M., Lambon Ralph, Matthew A., Madrid, Gaston, Patterson, Karalyn E.“…This proposed individual difference would account for the varying stage of decline at which patients with semantic dementia first show the reading impairment known as surface dyslexia. Recent neuroimaging data has provided validation of this view, showing that individual differences in degree of semantic reliance during exception word reading predict the amount of activation in left anterior temporal regions associated with semantic processing. …”
Publicado 2016
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1127por Woodbury-Smith, M., Bilder, D. A., Morgan, J., Jerominski, L., Darlington, T., Dyer, T., Paterson, A. D., Coon, H.“…CONCLUSIONS: Although this region does not overlap with ASD linkage signals in these same samples, it has been associated with other psychiatric risk, including ADHD, developmental dyslexia, schizophrenia, specific language impairment, and juvenile bipolar disorder. …”
Publicado 2017
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1128por Borsani, Oscar, Piga, Daniela, Costa, Stefania, Govoni, Alessandra, Magri, Francesca, Artoni, Andrea, Cinnante, Claudia M., Fagiolari, Gigliola, Ciscato, Patrizia, Moggio, Maurizio, Bresolin, Nereo, Comi, Giacomo P., Corti, Stefania“…Stormorken syndrome is a rare autosomal dominant disease that is characterized by a complex phenotype that includes tubular aggregate myopathy (TAM), bleeding diathesis, hyposplenism, mild hypocalcemia and additional features, such as miosis and a mild intellectual disability (dyslexia). Stormorken syndrome is caused by autosomal dominant mutations in the STIM1 gene, which encodes an endoplasmic reticulum Ca(2+) sensor. …”
Publicado 2018
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1129“…Previous studies have demonstrated that the ability to perceptually bind stimuli is impaired in various clinical conditions such as autism, dyslexia, schizophrenia, as well as aging. However, it remains unknown if adult-onset hearing loss, separate from aging, influences audiovisual temporal acuity. …”
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1130“…To assess the reading and spelling abilities the Hungarian version of the 3DM (Dyslexia Differential Diagnosis) was used. Cognitive abilities were tested using the Hungarian adaptation of the WISC-IV and the Rey Complex Figure Test. …”
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1132“…METHODS: A narrative synthesis of the findings is presented to highlight how AV rehabilitation impacts on patients with hemianopia including visual oculomotor function, functional ability in activities of daily living, hemianopic dyslexia, visual scanning and searching tasks, maintaining of functional ability post training and the effect on brain multisensory integration by using neuroimaging. …”
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1133“…OBJECTIVES/GOALS: Developmental dyslexia is a common reading disability (RD) which negatively impacts academic success. …”
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1134por Fraga-González, Gorka, Di Pietro, Sarah V., Pleisch, Georgette, Walitza, Susanne, Brandeis, Daniel, Karipidis, Iliana I., Brem, Silvia“…A combination of cross-sectional and longitudinal EEG data of a total of 62 children (35 female) at varying familial risk for dyslexia were available to form groups of 23, 22, 27, 27, and 42 participants for each of the five time points. …”
Publicado 2022
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1135por Schippers, Lessa M., Horstman, Lisa I., van de Velde, Hans, Pereira, Rob Rodrigues, Zinkstok, Janneke, Mostert, Jeanette C., Greven, Corina U., Hoogman, Martine“…Here we performed qualitative research to identify positive aspects and strengths associated with ADHD in a large convenience sample from the Dutch organization for people with ADHD, dyslexia and dyscalculia. We sent out open-ended questionnaires to the members of the organization, asking what they consider to be positive aspects of their ADHD. …”
Publicado 2022
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1136“…BACKGROUND: Theoretical models posit abnormalities in cortico-striatal pathways in two of the most common neurodevelopmental disorders (Developmental dyslexia, DD, and Attention deficit hyperactive disorder, ADHD), but it is still unclear what distinct cortico-striatal dysfunction might distinguish language disorders from others that exhibit very different symptomatology. …”
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1137“…KIAA0319, a well-studied candidate gene, has been shown to be associated with reading ability and developmental dyslexia. In the present study, we investigated whether KIAA0319 affects reading ability by interacting with the parental education level and whether rapid automatized naming (RAN), phonological awareness and morphological awareness mediate the relationship between KIAA0319 and reading ability. …”
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1138por Jenson, Ronda J., Lee, Michele S, Day, Arden D., Hughes, Amy E., Maroushek, Emma E., Roberts, Kelly D.“…Neurodiversity is a subgroup of neurodevelopmental conditions, such as autism, attention deficit disorder, dyslexia, dyspraxia, and other neurological conditions. …”
Publicado 2023
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1139“…CONCLUSION: What emerges from multiple studies is the essential role of timing deficits in the dorsal stream that are prevalent in developmental disorders like dyslexia, in aging, and following a TBI. Training visual dorsal stream function at low levels significantly improved high-level cognitive functions, including processing speed, selective and sustained attention, both auditory and visual working memory, problem solving, and reading fluency. …”
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1140por Kwok, Fu Yu, Wilkey, Eric D., Peters, Lien, Khiu, Ellyn, Bull, Rebecca, Lee, Kerry, Ansari, Daniel“…While significant advances have been made in characterizing the neural correlates of reading difficulties (developmental dyslexia), comparatively little is known about the neurobiological correlates of mathematical learning difficulties, such as developmental dyscalculia (DD). …”
Publicado 2023
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