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11241“…Separate investigations of cognitive abilities have established the prevalence of general intellectual impairment, although the actual extent to which a single individual is affected varies greatly within the population. …”
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11242“…Interviewees and other sources for the case study suggest the use of inspirational motivation, idealized influence, individualized consideration and intellectual stimulation, four factors in the transformational leadership model, had significant impact upon the attitudes and motivation of staff within KHCC. …”
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11243por Jusko, Todd A., Henderson, Charles R., Lanphear, Bruce P., Cory-Slechta, Deborah A., Parsons, Patrick J., Canfield, Richard L.“…CONCLUSIONS: Evidence from this cohort indicates that children’s intellectual functioning at 6 years of age is impaired by blood lead concentrations well below 10 μg/dL, the Centers for Disease Control and Prevention definition of an elevated blood lead level.…”
Publicado 2008
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11244“…Other clinical findings may include cardiac valve disease, reduced pulmonary function, hepatosplenomegaly, sinusitis, otitis media, hearing loss, sleep apnea, corneal clouding, carpal tunnel disease, and inguinal or umbilical hernia. Although intellectual deficit is generally absent in MPS VI, central nervous system findings may include cervical cord compression caused by cervical spinal instability, meningeal thickening and/or bony stenosis, communicating hydrocephalus, optic nerve atrophy and blindness. …”
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11245“…The tests were grouped into five main domains; (1) learning and memory, (2) visual scanning, planning and attention, (3) executive function, (4) visuo-motor speed and dexterity and (5) general intellectual ability RESULTS: No children in the study had test results in the clinical range in any domain. …”
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11246por Cho, Soo-Churl, Bhang, Soo-Young, Hong, Yun-Chul, Shin, Min-Sup, Kim, Boong-Nyun, Kim, Jae-Won, Yoo, Hee-Jung, Cho, In Hee, Kim, Hyo-Won“…OBJECTIVE: We investigated the relationship between the urinary concentrations of phthalate metabolites and children’s intellectual functioning. METHODS: This study enrolled 667 children at nine elementary schools in five South Korean cities. …”
Publicado 2010
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11247por Kamunyori, Sheila, Al-Bader, Sara, Sewankambo, Nelson, Singer, Peter A, Daar, Abdallah S“…Classified as a least developed country, Uganda has opted for exemptions from the TRIPS intellectual property protection regime that include permitting parallel importation and providing for compulsory licenses for pharmaceuticals. …”
Publicado 2010
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11248“…Lifestyle factors such as intellectual stimulation, cognitive and social engagement, nutrition, and various types of exercise appear to reduce the risk for common age-associated disorders such as Alzheimer’s disease (AD) and vascular dementia. …”
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11249por Freund, Romain, Le Ray, Camille, Charlier, Caroline, Avenell, Carolyn, Truster, Van, Tréluyer, Jean-Marc, Skalli, Dounia, Ville, Yves, Goffinet, François, Launay, Odile“…Determinants associated with non-vaccination in a multivariate logistic regression were: geographic origin (Sub-Saharan African origin, adjusted Odd Ratio aOR = 5.4[2.3–12.7], North African origin, aOR = 2.5[1.3–4.7] and Asian origin, aOR = 2.1[1.7–2.6] compared to French and European origin) and socio-professional categories (farmers, craftsmen and tradesmen, aOR = 2.3[2.0–2.6], intermediate professionals, aOR = 1.3[1.0–1.6], employees and manual workers, aOR = 2.5[1.4–4.4] compared to managers and intellectual professionals). The probability of not receiving pandemic flu vaccine was lower among women vaccinated against seasonal flu in the previous 5 years (aOR = 0.6[0.4–0.8]) and among those who stopped smoking before or early during pregnancy (aOR = 0.6[0.4–0.8]). …”
Publicado 2011
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11250por Lacaze, Catherine, Kauss, Tina, Kiechel, Jean-René, Caminiti, Antonella, Fawaz, Fawaz, Terrassin, Laurent, Cuart, Sylvie, Grislain, Luc, Navaratnam, Visweswaran, Ghezzoul, Bellabes, Gaudin, Karen, White, Nick J, Olliaro, Piero L, Millet, Pascal“…Lack of public funding was the main obstacle hampering the development process, and no intellectual property right was claimed. This approach resulted in a rapid technology transfer to the drug company Sanofi-Aventis, finalizing the process of development, registration and WHO pre-qualification of the fixed-dose co-formulation together with DNDi. …”
Publicado 2011
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11251“…In humans, loss of erlin function appears to cause progressive intellectual disability, motor dysfunction and joint contractures. …”
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11252por Chung, Ren-Hua, Ma, Deqiong, Wang, Kai, Hedges, Dale J, Jaworski, James M, Gilbert, John R, Cuccaro, Michael L, Wright, Harry H, Abramson, Ruth K, Konidari, Ioanna, Whitehead, Patrice L, Schellenberg, Gerard D, Hakonarson, Hakon, Haines, Jonathan L, Pericak-Vance, Margaret A, Martin, Eden R“…Deletions in the Xp22.2 to Xp22.3 region containing TBL1X and surrounding genes are associated with several genetic syndromes that include intellectual disability and autistic features. Our results, based on meta-analysis, joint analysis and replication analysis, suggest that TBL1X may play a role in ASD risk.…”
Publicado 2011
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11253por Poretti, Andrea, Vitiello, Giuseppina, Hennekam, Raoul CM, Arrigoni, Filippo, Bertini, Enrico, Borgatti, Renato, Brancati, Francesco, D'Arrigo, Stefano, Faravelli, Francesca, Giordano, Lucio, Huisman, Thierry AGM, Iannicelli, Miriam, Kluger, Gerhard, Kyllerman, Marten, Landgren, Magnus, Lees, Melissa M, Pinelli, Lorenzo, Romaniello, Romina, Scheer, Ianina, Schwarz, Christoph E, Spiegel, Ronen, Tibussek, Daniel, Valente, Enza Maria, Boltshauser, Eugen“…In the original report polydactyly, oral findings, intellectual disability, and absence of the cerebellar vermis at post-mortem characterized the syndrome. …”
Publicado 2012
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11254por Crowther, Caroline A, Aghajafari, Fariba, Askie, Lisa M, Asztalos, Elizabeth V, Brocklehurst, Peter, Bubner, Tanya K, Doyle, Lex W, Dutta, Sourabh, Garite, Thomas J, Guinn, Debra A, Hallman, Mikko, Hannah, Mary E, Hardy, Pollyanna, Maurel, Kimberly, Mazumder, Premasish, McEvoy, Cindy, Middleton, Philippa F, Murphy, Kellie E, Peltoniemi, Outi M, Peters, Dawn, Sullivan, Lisa, Thom, Elizabeth A, Voysey, Merryn, Wapner, Ronald J, Yelland, Lisa, Zhang, Sasha“…For the children, the primary study outcomes will be death or any neurological disability (however defined by trialists at childhood follow up and may include developmental delay or intellectual impairment (developmental quotient or intelligence quotient more than one standard deviation below the mean), cerebral palsy (abnormality of tone with motor dysfunction), blindness (for example, corrected visual acuity worse than 6/60 in the better eye) or deafness (for example, hearing loss requiring amplification or worse)). …”
Publicado 2012
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11255por Weissman, Charles, Zisk-Rony, Rachel Yaffa, Schroeder, Josh E, Weiss, Yoram G, Avidan, Alex, Elchalal, Uriel, Tandeter, Howard“…Selection of career specialties begins in earnest during the clinical rotations with exposure to the clinical and intellectual environments of various specialties. Career specialty selection is followed by choosing a residency program. …”
Publicado 2012
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11256por Cheillan, David, Curt, Marie Joncquel-Chevalier, Briand, Gilbert, Salomons, Gajja S, Mention-Mulliez, Karine, Dobbelaere, Dries, Cuisset, Jean-Marie, Lion-François, Laurence, Portes, Vincent Des, Chabli, Allel, Valayannopoulos, Vassili, Benoist, Jean-François, Pinard, Jean-Marc, Simard, Gilles, Douay, Olivier, Deiva, Kumaran, Afenjar, Alexandra, Héron, Delphine, Rivier, François, Chabrol, Brigitte, Prieur, Fabienne, Cartault, François, Pitelet, Gaëlle, Goldenberg, Alice, Bekri, Soumeya, Gerard, Marion, Delorme, Richard, Tardieu, Marc, Porchet, Nicole, Vianey-Saban, Christine, Vamecq, Joseph“…The only SLC6A8-deficient female patient in our series presented with the severe phenotype usually characterizing affected male patients, an observation in agreement with recent evidence that is in support of the fact that this X-linked disorder might be more frequent than expected in the female population with intellectual disability.…”
Publicado 2012
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11257por Raikkonen, Katri, Kajantie, Eero, Pesonen, Anu-Katriina, Heinonen, Kati, Alastalo, Hanna, Leskinen, Jukka T., Nyman, Kai, Henriksson, Markus, Lahti, Jari, Lahti, Marius, Pyhälä, Riikka, Tuovinen, Soile, Osmond, Clive, Barker, David J. P., Eriksson, Johan G.“…MAIN OUTCOME MEASURES: The Finnish Defense Forces Basic Intellectual Ability Test assessed twice over nearly five decades apart. …”
Publicado 2013
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11258por Hanchard, Neil A, Carvalho, Claudia MB, Bader, Patricia, Thome, Aaron, Omo-Griffith, Lisa, del Gaudio, Daniela, Pehlivan, Davut, Fang, Ping, Schaaf, Christian P, Ramocki, Melissa B, Lupski, James R, Cheung, Sau Wai“…BACKGROUND: Duplications of the X-linked MECP2 gene are associated with moderate to severe intellectual disability, epilepsy, and neuropsychiatric illness in males, while triplications are associated with a more severe phenotype. …”
Publicado 2012
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11259por Lopes, Alexandra M., Aston, Kenneth I., Thompson, Emma, Carvalho, Filipa, Gonçalves, João, Huang, Ni, Matthiesen, Rune, Noordam, Michiel J., Quintela, Inés, Ramu, Avinash, Seabra, Catarina, Wilfert, Amy B., Dai, Juncheng, Downie, Jonathan M., Fernandes, Susana, Guo, Xuejiang, Sha, Jiahao, Amorim, António, Barros, Alberto, Carracedo, Angel, Hu, Zhibin, Hurles, Matthew E., Moskovtsev, Sergey, Ober, Carole, Paduch, Darius A., Schiffman, Joshua D., Schlegel, Peter N., Sousa, Mário, Carrell, Douglas T., Conrad, Donald F.“…By contrasting the properties of our case-specific CNVs with those of CNV callsets from cases of autism, schizophrenia, bipolar disorder, and intellectual disability, we propose that the CNV burden in spermatogenic impairment is distinct from the burden of large, dominant mutations described for neurodevelopmental disorders. …”
Publicado 2013
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11260por Davidovic, Laetitia, Durand, Nelly, Khalfallah, Olfa, Tabet, Ricardo, Barbry, Pascal, Mari, Bernard, Sacconi, Sabrina, Moine, Hervé, Bardoni, Barbara“…The Fragile X-Related 1 gene (FXR1) is a paralog of the Fragile X Mental Retardation 1 gene (FMR1), whose absence causes the Fragile X syndrome, the most common form of inherited intellectual disability. FXR1P plays an important role in normal muscle development, and its absence causes muscular abnormalities in mice, frog, and zebrafish. …”
Publicado 2013
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