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11401“…Adolescents (12–17) with at least one self-harm episode in the previous 6 months referred for community treatment, who had no intellectual disability, psychosis or autism were eligible for START. …”
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11402por Gonda, Kenji, Akama, Takanori, Nakamura, Takayuki, Hashimoto, Eiko, Kyoya, Naomi, Rokkaku, Yuichi, Maejima, Yuko, Horita, Shoichiro, Tachibana, Kazunoshin, Abe, Noriko, Ohtake, Tohru, Shimomura, Kenju, Kono, Koji, Saji, Shigehira, Takenoshita, Seiichi, Higashihara, Eiji“…Another brother had a syndrome of kidney failure, intellectual disability, and diabetes mellitus, which seemed to be caused by mutation in the CREBBP gene. …”
Publicado 2019
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11403por Marshall, Helen, McMillan, Mark, Wang, Bing, Booy, Robert, Afzali, Hossein, Buttery, Jim, Blyth, Christopher C, Richmond, Peter, Shaw, David, Gordon, David, Barton, Belinda“…Primary outcome measures include general intellectual functioning from the Wechsler Adult Intelligence Scale and overall quality of life from the Health Utilities Index. …”
Publicado 2019
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11404por Zhuang, Yuan, Xu, Haifeng C, Shinde, Prashant V, Warfsmann, Jens, Vasilevska, Jelena, Sundaram, Balamurugan, Behnke, Kristina, Huang, Jun, Hoell, Jessica I, Borkhardt, Arndt, Pfeffer, Klaus, Taha, Mohamed S, Herebian, Diran, Mayatepek, Ertan, Brenner, Dirk, Ahmadian, Mohammad Reza, Keitel, Verena, Wieczorek, Dagmar, Häussinger, Dieter, Pandyra, Aleksandra A, Lang, Karl S, Lang, Philipp A“…OBJECTIVE: The Fragile X mental retardation (FMR) syndrome is a frequently inherited intellectual disability caused by decreased or absent expression of the FMR protein (FMRP). …”
Publicado 2020
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11405por Neth, Bryan J., Graff-Radford, Jonathan, Mielke, Michelle M., Przybelski, Scott A., Lesnick, Timothy G., Schwarz, Christopher G., Reid, Robert I., Senjem, Matthew L., Lowe, Val J., Machulda, Mary M., Petersen, Ronald C., Jr., Clifford R. Jack, Knopman, David S., Vemuri, Prashanthi“…METHODS: We examined multimodal [structural and diffusion Magnetic Resonance Imaging (MRI), FDG PET] neuroimaging measures in 50–65 year olds to examine the associations between risk factors (Intellectual/Physical Activity: education-occupation composite, physical, and cognitive-based activity engagement; General Health Factors: presence of cardiovascular and metabolic conditions (CMC), body mass index, hemoglobin A1c, smoking status (ever/never), CAGE Alcohol Questionnaire (>2, yes/no), Beck Depression Inventory score), brain reserve measures [Dynamic: genu corpus callosum fractional anisotropy (FA), posterior cingulate cortex FDG uptake, superior parietal cortex thickness, AD signature cortical thickness; Static: intracranial volume], and cognition (global, memory, attention, language, visuospatial) from a population-based sample. …”
Publicado 2020
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11406por Startin, Carla M., D’Souza, Hana, Ball, George, Hamburg, Sarah, Hithersay, Rosalyn, Hughes, Kate M. O., Massand, Esha, Karmiloff-Smith, Annette, Thomas, Michael S. C., Strydom, Andre“…BACKGROUND: Down syndrome (DS) is associated with variable intellectual disability and multiple health and psychiatric comorbidities. …”
Publicado 2020
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11407por Melby, Linde, Indredavik, Marit S., Løhaugen, Gro, Brubakk, Ann Mari, Skranes, Jon, Vik, Torstein“…Previous studies have shown that individuals with intellectual disability, IQ < 70, have increased risk of being diagnosed with one or more mental disorders. …”
Publicado 2020
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11408por Pei, Ya-ping, Wang, Yue-yi, Liu, Dan, Lei, Hui-yang, Yang, Zhi-hao, Zhang, Zi-wei, Han, Man, Cheng, Ke, Chen, Yu-shan, Li, Jin-quan, Cheng, Gui-rong, Xu, Lang, Wu, Qing-ming, McClintock, Shawn M., Yang, Ying, Zhang, Yong, Zeng, Yan“…Fragile X syndrome (FXS) is the most common inherited form of intellectual disability, resulted from the silencing of the Fmr1 gene and the subsequent loss of fragile X mental retardation protein (FMRP). …”
Publicado 2020
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11409Publicado 2020“…Undernourished children are more likely to experience cognitive, physical, and metabolic developmental impairments that can lead to later cardiovascular disease, reduced intellectual ability and school attainment, and reduced economic productivity in adulthood(2). …”
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11410por Liao, Jianxiang, Huang, Tieshuan, Srour, Myriam, Xiao, Yuhan, Chen, Yan, Lin, Sufang, Chen, Li, Hu, Yan, Men, Lina, Wen, Jialun, Li, Bing, Wen, Feiqiu, Xiong, Lan“…However, the long-term outcomes were extremely poor in the patients with defined electro-clinical epilepsy syndromes, including severe motor and intellectual developmental deficits (follow-up of 4.94 ± 1.56 years), despite early diagnosis and treatment. …”
Publicado 2020
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11411por da Cruz Netto, Ovidio Lopes, Rodrigues, Silvia Cristina Martini, de Castro, Marcus Vasconcelos, da Silva, Diego Pereira, da Silva, Robson Rodrigues, de Souza, Richard Ribeiro Brancato, de Souza, Adriana A. Ferreira, Bissaco, Marcia Aparecida Silva“…The work involved a multidisciplinary team and assessed the effectiveness of the test performed by 30 children with Down syndrome from APAE, a special education school for children with intellectual disabilities in São Paulo, Brazil. The children were separated into two groups (Experimental - GE and Control - GC) with homogeneity and normality of the data. …”
Publicado 2020
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11412por Husson, Thomas, Lecoquierre, François, Cassinari, Kevin, Charbonnier, Camille, Quenez, Olivier, Goldenberg, Alice, Guerrot, Anne-Marie, Richard, Anne-Claire, Drouin-Garraud, Valérie, Brehin, Anne-Claire, Soleimani, Maryam, Taton, Romain, Rotharmel, Maud, Rosier, Antoine, Chambon, Pascal, Le Meur, Nathalie, Joly-Helas, Géraldine, Saugier-Veber, Pascale, Boland, Anne, Deleuze, Jean-François, Olaso, Robert, Frebourg, Thierry, Nicolas, Gael, Guillin, Olivier, Campion, Dominique“…We have performed whole-exome sequencing to identify both nucleotide variants and copy number variants (CNVs) in 253 ASD patients, including 68 patients with intellectual disability (ID) and 90 diagnosed as Asperger syndrome. …”
Publicado 2020
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11413por Rousseau, Marie-Christine, Baumstarck, Karine, Valkov, Maria, Felce, Agnés, Brisse, Catherine, Khaldi-Cherif, Sherezad, Loundou, Anderson, Auquier, Pascal, Billette de Villemeur, Thierry“…OBJECTIVES: Polyhandicap (PLH), defined by a combination of profound intellectual impairment and serious motor deficits, is a severe condition with complex disabilities. …”
Publicado 2020
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11414“…MAIN OUTCOMES AND MEASURES: The primary outcomes were extended perinatal mortality and a record of SEN (≥1 of intellectual disabilities, dyslexia, physical or motor impairment, language or speech disorder, autistic spectrum disorder, and social, emotional, or behavioral difficulties) at school (children aged 4-18 years). …”
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11415por Bauer, Michael, Kölsch, Uwe, Krüger, Renate, Unterwalder, Nadine, Hameister, Karin, Kaiser, Fabian Marc, Vignoli, Aglaia, Rossi, Rainer, Botella, Maria Pilar, Budisteanu, Magdalena, Rosello, Monica, Orellana, Carmen, Tejada, Maria Isabel, Papuc, Sorina Mihaela, Patat, Oliver, Julia, Sophie, Touraine, Renaud, Gomes, Thusari, Wenner, Kirsten, Xu, Xiu, Afenjar, Alexandra, Toutain, Annick, Philip, Nicole, Jezela-Stanek, Aleksandra, Gortner, Ludwig, Martinez, Francisco, Echenne, Bernard, Wahn, Volker, Meisel, Christian, Wieczorek, Dagmar, El-Chehadeh, Salima, Van Esch, Hilde, von Bernuth, Horst“…MECP2 (methyl CpG binding protein 2) duplication causes syndromic intellectual disability. Patients often suffer from life-threatening infections, suggesting an additional immunodeficiency. …”
Publicado 2015
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11416por Fregeac, Julien, Moriceau, Stéphanie, Poli, Antoine, Nguyen, Lam Son, Oury, Franck, Colleaux, Laurence“…BACKGROUND: Formation and maintenance of appropriate neural networks require tight regulation of neural stem cell proliferation, differentiation, and neurogenesis. microRNAs (miRNAs) play an important role in brain development and plasticity, and dysregulated miRNA profiles have been linked to neurodevelopmental disorders including autism, schizophrenia, or intellectual disability. Yet, the functional role of miRNAs in neural development and postnatal brain functions remains unclear. …”
Publicado 2020
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11417por Tulchinsky, Theodore H.“…This more holistic approach to population health has become a leading element in modern public health largely based on the intellectual contribution of Marc Lalonde.…”
Publicado 2018
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11418por Lilamand, Matthieu, Porte, Baptiste, Cognat, Emmanuel, Hugon, Jacques, Mouton-Liger, François, Paquet, Claire“…These nutritional interventions are validated treatments of pharmacoresistant epilepsy, consequently leading to a better intellectual development in epileptic children. In neurodegenerative diseases and cognitive decline, potential benefits of KD were previously pointed out, but the published evidence remains scarce. …”
Publicado 2020
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11419por Zhao, Qian, Tian, Zhiyuan, Zhou, Guoyu, Niu, Qiang, Chen, Jingwen, Li, Pei, Dong, Lixin, Xia, Tao, Zhang, Shun, Wang, Aiguo“…Noteworthy, epidemiological data indicated intimate correlations between disturbed circulating levels of mitochondrial biogenesis signaling molecules and fluoride-caused intellectual loss in children. Conclusions: Our data suggest the pivotal role of impaired mitochondrial biogenesis in developmental fluoride neurotoxicity and the underlying SIRT1 signaling dysfunction in such neurotoxic process, which emphasizes RSV as a potential therapeutic dietary agent for relieving developmental fluoride neurotoxicity.…”
Publicado 2020
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11420por Cuvertino, Sara, Hartill, Verity, Colyer, Alice, Garner, Terence, Nair, Nisha, Al-Gazali, Lihadh, Canham, Natalie, Faundes, Victor, Flinter, Frances, Hertecant, Jozef, Holder-Espinasse, Muriel, Jackson, Brian, Lynch, Sally Ann, Nadat, Fatima, Narasimhan, Vagheesh M., Peckham, Michelle, Sellers, Robert, Seri, Marco, Montanari, Francesca, Southgate, Laura, Squeo, Gabriella Maria, Trembath, Richard, van Heel, David, Venuto, Santina, Weisberg, Daniel, Stals, Karen, Ellard, Sian, Barton, Anne, Kimber, Susan J., Sheridan, Eamonn, Merla, Giuseppe, Stevens, Adam, Johnson, Colin A., Banka, Siddharth“…None of the individuals had intellectual disability. The frequency of clinical features, objective software-based facial analysis metrics, and genome-wide peripheral blood DNA methylation patterns in these patients were significantly different from that of KS1. …”
Publicado 2020
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