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11961por Sagué Vilavella, M., Giménez Palomo, A., Àvila-Parcet, A., Fernández Plaza, T., Navarro Cortés, L., Oretega Hernández, G., Pons Cabrera, M., Tardón Senabre, L., Vázquez, M.“…RESULTS: A 26-year-old woman from Barcelona (Catalonia, Spain), diagnosed with mild intellectual disability, made 1447 emergency visits between 2009 and 2021 (figure 1). 946 visits (65%) took place in psychiatric emergency departments (EDs), whilst 353 (24%) in non-psychiatric EDs and 148 (10%) in urgent primary care. …”
Publicado 2023
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11962por Fasham, James, Huebner, Antje K, Liebmann, Lutz, Khalaf-Nazzal, Reham, Maroofian, Reza, Kryeziu, Nderim, Wortmann, Saskia B, Leslie, Joseph S, Ubeyratna, Nishanka, Mancini, Grazia M S, van Slegtenhorst, Marjon, Wilke, Martina, Haack, Tobias B, Shamseldin, Hanan E, Gleeson, Joseph G, Almuhaizea, Mohamed, Dweikat, Imad, Abu-Libdeh, Bassam, Daana, Muhannad, Zaki, Maha S, Wakeling, Matthew N, McGavin, Lucy, Turnpenny, Peter D, Alkuraya, Fowzan S, Houlden, Henry, Schlattmann, Peter, Kaila, Kai, Crosby, Andrew H, Baple, Emma L, Hübner, Christian A“…The cardinal clinical features of the condition include hypotonia in infancy, delayed psychomotor development across all domains and intellectual impairment. Affected individuals commonly display traits associated with autistic spectrum disorder including anxiety, hyperactivity and stereotyped movements. …”
Publicado 2023
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11963por Meng, Linxue, Huang, Dishu, Xie, Lingling, Song, Xiaojie, Luo, Hanyu, Gui, Jianxiong, Ding, Ran, Zhang, Xiaofang, Jiang, Li“…The efficacy of perampanel (PMP) in treating seizures and intellectual disability was apparent. Furthermore, 43 cases of ROGDI-related KTS were retrieved. 100% exhibited epilepsy, global developmental delay, and amelogenesis imperfecta. 17.2% received a diagnosis of attention deficit hyperactivity disorder (ADHD), and 3.4% were under suspicion of autism spectrum disorder (ASD). …”
Publicado 2023
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11964“…Children (11 boys, 7 girls) represented the spectrum of motor functioning, with comorbidities including epilepsy, intellectual disability, and communication impairments. …”
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11965por Francés, Lorena, Ruiz, Antoni, Soler, C. Virgínia, Francés, Joan, Caules, Jessica, Hervás, Amaia, Carretero, Carolina, Cardona, Bárbara, Quezada, Elizabeth, Fernández, Alberto, Quintero, Javier“…A total of 2.4% presented autism spectrum disorder (ASD); 14% presented attention-deficit hyperactivity disorder (ADHD); 0.34% presented mild intellectual disability; 9.54% presented communication disorder (CD) (5.8% language disorder, 3.4% phonological disorder, and 0.34% stuttering); 10% presented learning disorder with reading difficulties; 5.8% presented learning disorder with difficulties in writing; 3.11% presented learning disorder with difficulties in mathematics; 1% presented transitory tic disorder; 0.34% presented chronic tic disorder; 1% presented Tourette syndrome; 2% presented motor coordination disorder (MCD); and 0.34% presented stereotypic movement disorders. …”
Publicado 2023
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11966por Alsaad, Ali J., Al Khamees, Mujtaba M., Alkadi, Abdulelah N., Alsaleh, Majd A., Alshairdah, Aeshah S., Alessa, Zahra’a A.“…BACKGROUND: Neurodevelopmental disorders (NDDs) are a group of conditions that include attention-deficit/hyperactivity disorders, specific learning disorders, autism spectrum disorder, intellectual disability, and other disorders. Raising a child with an NDD can be difficult because it affects the social lives of the parents and their relationships. …”
Publicado 2023
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11967por Harvard, Chansonette, Strong, Emma, Mercier, Eloi, Colnaghi, Rita, Alcantara, Diana, Chow, Eva, Martell, Sally, Tyson, Christine, Hrynchak, Monica, McGillivray, Barbara, Hamilton, Sara, Marles, Sandra, Mhanni, Aziz, Dawson, Angelika J, Pavlidis, Paul, Qiao, Ying, Holden, Jeanette J, Lewis, Suzanne ME, O'Driscoll, Mark, Rajcan-Separovic, Evica“…BACKGROUND: 1q21.1 Copy Number Variant (CNV) is associated with a highly variable phenotype ranging from congenital anomalies, learning deficits/intellectual disability (ID), to a normal phenotype. …”
Publicado 2011
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11968por Mefford, Heather C, Rosenfeld, Jill A, Shur, Natasha, Slavotinek, Anne M, Cox, Victoria A, Hennekam, Raoul C, Firth, Helen V, Willatt, Lionel, Wheeler, Patricia, Morrow, Eric M, Cook, Joseph, Sullivan, Rachel, Oh, Albert, McDonald, Marie T, Zonana, Jonathan, Keller, Kory, Hannibal, Mark C, Ball, Susie, Kussmann, Jennifer, Gorski, Jerome, Zelewski, Susan, Banks, Valerie, Smith, Wendy, Smith, Rosemarie, Paull, Lindsay, Rosenbaum, Kenneth N, Amor, David J, Silva, Joao, Lamb, Allen, Eichler, Evan E“…BACKGROUND: Chromosome 15q24 microdeletion syndrome is a rare genomic disorder characterised by intellectual disability, growth retardation, unusual facial morphology and other anomalies. …”
Publicado 2011
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11969por Cukier, Holly N, Dueker, Nicole D, Slifer, Susan H, Lee, Joycelyn M, Whitehead, Patrice L, Lalanne, Eminisha, Leyva, Natalia, Konidari, Ioanna, Gentry, Ryan C, Hulme, William F, Booven, Derek Van, Mayo, Vera, Hofmann, Natalia K, Schmidt, Michael A, Martin, Eden R, Haines, Jonathan L, Cuccaro, Michael L, Gilbert, John R, Pericak-Vance, Margaret A“…A subset of these genes has been implicated in other neurobehavioral disorders including depression (SLIT3), epilepsy (CLCN2, PRICKLE1), intellectual disability (AP4M1), schizophrenia (WDR60), and Tourette syndrome (OFCC1). …”
Publicado 2014
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11970“…We built the Memorial brand around the flame of individual passion ignited by the four intelligences: spiritual, emotional, intellectual, and physical. We enlisted the executive leaders as our “fire starters,” charging them with being the “Keepers of the Flame.” …”
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11971por Serret, Sylvie, Hun, Stephanie, Iakimova, Galina, Lozada, Jose, Anastassova, Margarita, Santos, Andreia, Vesperini, Stephanie, Askenazy, Florence“…We have developed a computer-based game called JeStiMulE based on logical skills to teach emotions to individuals with ASC, independently of their age, intellectual, verbal and academic level. The aim of the present study was to verify the usability of JeStiMulE (which is its adaptability, effectiveness and efficiency) on a heterogeneous ASC group. …”
Publicado 2014
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11972por D’Angelo, Carla S, Varela, Monica C, de Castro, Cláudia IE, Kim, Chong A, Bertola, Débora R, Lourenço, Charles M, Perez, Ana Beatriz A, Koiffmann, Celia P“…BACKGROUND: Certain rare syndromes with developmental delay or intellectual disability caused by genomic copy number variants (CNVs), either deletions or duplications, are associated with higher rates of obesity. …”
Publicado 2014
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11973por Tabet, Anne-Claude, Verloes, Alain, Pilorge, Marion, Delaby, Elsa, Delorme, Richard, Nygren, Gudrun, Devillard, Françoise, Gérard, Marion, Passemard, Sandrine, Héron, Delphine, Siffroi, Jean-Pierre, Jacquette, Aurelia, Delahaye, Andrée, Perrin, Laurence, Dupont, Céline, Aboura, Azzedine, Bitoun, Pierre, Coleman, Mary, Leboyer, Marion, Gillberg, Christopher, Benzacken, Brigitte, Betancur, Catalina“…BACKGROUND: Apparently balanced chromosomal rearrangements can be associated with an abnormal phenotype, including intellectual disability and autism spectrum disorder (ASD). …”
Publicado 2015
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11974por Koschack, Janka, Weibezahl, Lara, Friede, Tim, Himmel, Wolfgang, Makedonski, Philip, Grabowski, Jens“…But we should be cautious to interpret this dissociation as a sign of an intellectual incapability to understand scientific evidence or a naïve trust in experiential knowledge. …”
Publicado 2015
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11975por Mroske, Cameron, Rasmussen, Kristen, Shinde, Deepali N., Huether, Robert, Powis, Zoe, Lu, Hsiao-Mei, Baxter, Ruth M., McPherson, Elizabeth, Tang, Sha“…Further, recent independent reports describe two unrelated families in whom p.E1799K co-segregated with megalencephaly and intellectual disability (ID); in both cases, p.E1799K was shown to have originated due to germline mosaicism. …”
Publicado 2015
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11976por Brasa, Sarah, Mueller, Arne, Jacquemont, Sébastien, Hahne, Florian, Rozenberg, Izabela, Peters, Thomas, He, Yunsheng, McCormack, Christine, Gasparini, Fabrizio, Chibout, Salah-Dine, Grenet, Olivier, Moggs, Jonathan, Gomez-Mancilla, Baltazar, Terranova, Rémi“…BACKGROUND: Fragile X syndrome (FXS) is the most common form of inherited intellectual disability, resulting from the loss of function of the fragile X mental retardation 1 (FMR1) gene. …”
Publicado 2016
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11977por Tilahun, Dejene, Hanlon, Charlotte, Fekadu, Abebaw, Tekola, Bethlehem, Baheretibeb, Yonas, Hoekstra, Rosa A.“…The majority (66.7 %; n = 68) had a diagnosis of intellectual disability (ID); 34 children (33.3 %) had autism spectrum disorder (ASD) as their primary diagnosis. …”
Publicado 2016
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11978“…BACKGROUND: The RNA polymerase II transcriptional Mediator subunit Med12 is broadly implicated in vertebrate brain development, and genetic variation in human MED12 is associated with X-linked intellectual disability and neuropsychiatric disorders. …”
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11979por Bennett, Deborah, Bellinger, David C., Birnbaum, Linda S., Bradman, Asa, Chen, Aimin, Cory-Slechta, Deborah A., Engel, Stephanie M., Fallin, M. Daniele, Halladay, Alycia, Hauser, Russ, Hertz-Picciotto, Irva, Kwiatkowski, Carol F., Lanphear, Bruce P., Marquez, Emily, Marty, Melanie, McPartland, Jennifer, Newschaffer, Craig J., Payne-Sturges, Devon, Patisaul, Heather B., Perera, Frederica P., Ritz, Beate, Sass, Jennifer, Schantz, Susan L., Webster, Thomas F., Whyatt, Robin M., Woodruff, Tracey J., Zoeller, R. Thomas, Anderko, Laura, Campbell, Carla, Conry, Jeanne A., DeNicola, Nathaniel, Gould, Robert M., Hirtz, Deborah, Huffling, Katie, Landrigan, Philip J., Lavin, Arthur, Miller, Mark, Mitchell, Mark A., Rubin, Leslie, Schettler, Ted, Tran, Ho Luong, Acosta, Annie, Brody, Charlotte, Miller, Elise, Miller, Pamela, Swanson, Maureen, Witherspoon, Nsedu Obot“…Summary: Children in America today are at an unacceptably high risk of developing neurodevelopmental disorders that affect the brain and nervous system including autism, attention deficit hyperactivity disorder, intellectual disabilities, and other learning and behavioral disabilities. …”
Publicado 2016
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11980por Kovshoff, Hanna, Banaschewski, Tobias, Buitelaar, Jan K., Carucci, Sara, Coghill, David, Danckaerts, Marina, Dittmann, Ralf W., Falissard, Bruno, Grimshaw, Dina Gojkovic, Hollis, Chris, Inglis, Sarah, Konrad, Kerstin, Liddle, Elizabeth, McCarthy, Suzanne, Nagy, Peter, Thompson, Margaret, Wong, Ian C.K., Zuddas, Alessandro, Sonuga-Barke, Edmund J.S.“…Methods: Following a literature search aimed at identifying associations between MPH and cognition and/or motivation, a qualitative semistructured interview was designed to focus specifically on the domains of cognition (i.e., reasoning, depth/breadth of thinking, intellectual capacity, and creativity) and motivation (i.e., drive, effort, and attitudes toward rewards/incentives). …”
Publicado 2016
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