Materias dentro de su búsqueda.
Materias dentro de su búsqueda.
Historia
22
Intelectuales
12
Filosofía
11
Intellectual life
9
Vida intelectual
8
History
7
Derechos de autor
6
Administración
4
Educación
4
Filósofos
4
Inteligencia
4
Política y gobierno
4
Ciencia política
3
Civilización
3
Etnología
3
Filosofía moderna
3
Física
3
Historia y crítica
3
Propiedad intelectual
3
Teoría del conocimiento
3
American literature
2
Antropología filosófica
2
Biografías
2
Capital intelectual
2
Ciencia
2
Civilización antigua
2
Civilización moderna
2
Cognición en niños
2
Condiciones sociales
2
Copyright
2
-
10581por Moncaster, Juliet A., Pineda, Roberto, Moir, Robert D., Lu, Suqian, Burton, Mark A., Ghosh, Joy G., Ericsson, Maria, Soscia, Stephanie J., Mocofanescu, Anca, Folkerth, Rebecca D., Robb, Richard M., Kuszak, Jer R., Clark, John I., Tanzi, Rudolph E., Hunter, David G., Goldstein, Lee E.“…Down syndrome (DS, trisomy 21) is the most common chromosomal disorder and the leading genetic cause of intellectual disability in humans. In DS, triplication of chromosome 21 invariably includes the APP gene (21q21) encoding the Alzheimer's disease (AD) amyloid precursor protein (APP). …”
Publicado 2010
Enlace del recurso
Enlace del recurso
Enlace del recurso
Texto -
10582por Durkin, Maureen S., Maenner, Matthew J., Meaney, F. John, Levy, Susan E., DiGuiseppi, Carolyn, Nicholas, Joyce S., Kirby, Russell S., Pinto-Martin, Jennifer A., Schieve, Laura A.“…The SES gradient was significantly stronger in children with a pre-existing diagnosis than in those meeting criteria for ASD but with no previous record of an ASD diagnosis (p<0.001), and was not present in children with co-occurring ASD and intellectual disability. CONCLUSIONS: The stronger SES gradient in ASD prevalence in children with versus without a pre-existing ASD diagnosis points to potential ascertainment or diagnostic bias and to the possibility of SES disparity in access to services for children with autism. …”
Publicado 2010
Enlace del recurso
Enlace del recurso
Enlace del recurso
Texto -
10583“…The neurological features of JSRD include hypotonia, ataxia, developmental delay, intellectual disability, abnormal eye movements, and neonatal breathing dysregulation. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Texto -
10584“…Other manifestations vary between patients in their nature and severity and include frequent episodes of acute liver failure, renal dysfunction, exocrine pancreas insufficiency, intellectual deficit, hypothyroidism, neutropenia and recurrent infections. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Texto -
10585por Reyes-García, Victoria“…CONCLUSIONS: Ethical considerations in the ethnopharmacology of the 21st century should go beyond the recognition of the Intellectual Property Rights or the acquisition of research permits, to include considerations on the healthcare of the original holders of ethnopharmacological knowledge. …”
Publicado 2010
Enlace del recurso
Enlace del recurso
Enlace del recurso
Texto -
10586por Qi, Hank H., Sarkissian, Madathia, Hu, Gang-Qing, Wang, Zhibin, Bhattacharjee, Arindam, Gordon, D. Benjamin, Gonzales, Michelle, Lan, Fei, Ongusaha, Pat P., Huarte, Maite, Yaghi, Nasser K., Lim, Huijun, Garcia, Benjamin A., Brizuela, Leonardo, Zhao, Keji, Roberts, Thomas M., Shi, Yang“…X-linked mental retardation (XLMR) is a complex human disease that causes intellectual disability1. Causal mutations have been found in approximately 90 X-linked genes2; however, molecular and biological functions of many of these genetically defined XLMR genes remain unknown. …”
Publicado 2010
Enlace del recurso
Enlace del recurso
Enlace del recurso
Texto -
10587por McCarthy, Mark“…Two of six thematic sessions related to research: one was solely concerned with drug development and the protection of intellectual property. Two European Union-supported health research projects in India show a similar trend. …”
Publicado 2011
Enlace del recurso
Enlace del recurso
Enlace del recurso
Texto -
10588“…Government and civil society reaction to expected increases in drug prices precipitated a series of events challenging these rules, culminating in the 2001 World Trade Organization's Doha Declaration on the Agreement on Trade-Related Aspects of Intellectual Property Rights and Public Health. The Declaration affirmed that patent rules should be interpreted and implemented to protect public health and to promote access to medicines for all. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Texto -
10589por Shrivatava, Amresh“…There was neither dedicated time nor any funding for conducting research. It came from the intellectual insight of our fore fathers in the field of mental health to gradually grow to the state of strategic education in research, training in research, international research collaborations and setting up of internationally accredited centers. …”
Publicado 2010
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10590“…Fragile X syndrome (FXS), caused by loss of the fragile X mental retardation 1 (FMR1) product (FMRP), is the most common cause of inherited intellectual disability and autism spectrum disorders. …”
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10591por Sheridan, Steven D., Theriault, Kraig M., Reis, Surya A., Zhou, Fen, Madison, Jon M., Daheron, Laurence, Loring, Jeanne F., Haggarty, Stephen J.“…Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. In addition to cognitive deficits, FXS patients exhibit hyperactivity, attention deficits, social difficulties, anxiety, and other autistic-like behaviors. …”
Publicado 2011
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10592por Strømme, Petter, Dobrenis, Kostantin, Sillitoe, Roy V., Gulinello, Maria, Ali, Nafeeza F., Davidson, Cristin, Micsenyi, Matthew C., Stephney, Gloria, Ellevog, Linda, Klungland, Arne, Walkley, Steven U.“…Three resulting phenotypes have so far been reported: an X-linked Angelman syndrome-like condition, Christianson syndrome and corticobasal degeneration with tau deposition, with each characterized by severe intellectual disability, epilepsy, autistic behaviour and ataxia. …”
Publicado 2011
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10593por Parvez, Faruque, Wasserman, Gail A., Factor-Litvak, Pam, Liu, Xinhua, Slavkovich, Vesna, Siddique, Abu B., Sultana, Rebeka, Sultana, Ruksana, Islam, Tariqul, Levy, Diane, Mey, Jacob L., van Geen, Alexander, Khan, Khalid, Kline, Jennie, Ahsan, Habibul, Graziano, Joseph H.“…Background: Several reports indicate that drinking water arsenic (WAs) and manganese (WMn) are associated with children’s intellectual function. Very little is known, however, about possible associations with other neurologic outcomes such as motor function. …”
Publicado 2011
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10594por Bouchard, Maryse F., Chevrier, Jonathan, Harley, Kim G., Kogut, Katherine, Vedar, Michelle, Calderon, Norma, Trujillo, Celina, Johnson, Caroline, Bradman, Asa, Barr, Dana Boyd, Eskenazi, Brenda“…Conclusions: Prenatal but not postnatal urinary DAP concentrations were associated with poorer intellectual development in 7-year-old children. Maternal urinary DAP concentrations in the present study were higher but nonetheless within the range of levels measured in the general U.S. population.…”
Publicado 2011
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10595por Stewart, Larissa R, Hall, April L, Kang, Sung-Hae L, Shaw, Chad A, Beaudet, Arthur L“…BACKGROUND: Many copy number variants (CNVs) are documented to be associated with neuropsychiatric disorders, including intellectual disability, autism, epilepsy, schizophrenia, and bipolar disorder. …”
Publicado 2011
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10596por Berry, Jay G., Poduri, Annapurna, Bonkowsky, Joshua L., Zhou, Jing, Graham, Dionne A., Welch, Chelsea, Putney, Heather, Srivastava, Rajendu“…Children with NI were identified with International Classification of Diseases, 9th Revision, Clinical Modification diagnoses resulting in functional and/or intellectual impairment. We assessed trends in inpatient resource utilization for children with NI with a Mantel-Haenszel chi-square test using all 4 y of data combined. …”
Publicado 2012
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10597por Ersland, Kari M., Christoforou, Andrea, Stansberg, Christine, Espeseth, Thomas, Mattheisen, Manuel, Mattingsdal, Morten, Hardarson, Gudmundur A., Hansen, Thomas, Fernandes, Carla P. D., Giddaluru, Sudheer, Breuer, René, Strohmaier, Jana, Djurovic, Srdjan, Nöthen, Markus M., Rietschel, Marcella, Lundervold, Astri J., Werge, Thomas, Cichon, Sven, Andreassen, Ole A., Reinvang, Ivar, Steen, Vidar M., Le Hellard, Stephanie“…CONCLUSION: Our gene-based approach suggests that RORB could be involved in verbal intelligence differences, while the genes enriched in the temporal cortex might be important to intellectual functions as measured by a test of reasoning in the healthy population. …”
Publicado 2012
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10598por Lee, Ok Jeong, Kim, Su-Jin, Sohn, Young Bae, Park, Hyung-Doo, Lee, Soo-Youn, Kim, Chi-Hwa, Ko, Ah-Ra, Yook, Yeon-Joo, Lee, Su-Jin, Park, Sung Won, Kim, Se-Hwa, Cho, Sung-Yoon, Kwon, Eun-Kyung, Han, Sun Ju, Jin, Dong-Kyu“…We classified 43 Hunter syndrome patients as having attenuated or severe disease types based on clinical characteristics, especially intellectual and cognitive status. There were 27 patients with the severe type and 16 with the attenuated type. …”
Publicado 2012
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10599por Knox, Andrew, Schneider, Andrea, Abucayan, Floridette, Hervey, Crystal, Tran, Christina, Hessl, David, Berry-Kravis, Elizabeth“…Only minor differences in performance on the KiTAP were seen between mental age-matched cohorts of subjects with FXS and non-FXS intellectual disability. CONCLUSIONS: The KiTAP can be administered to cohorts with FXS over a wide range of function with valid reproducible scores. …”
Publicado 2012
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto -
10600por Schälte, Gereon, Stoppe, Christian, Rossaint, Rolf, Gilles, Laura, Heuser, Maike, Rex, Steffen, Coburn, Mark, Zoremba, Norbert, Rieg, Annette“…This indicates some basic procedural understanding and intellectual transfer in principle. Operating errors (n = 91) were frequently not recognized and corrected (n = 77). …”
Publicado 2012
Enlace del recurso
Enlace del recurso
Enlace del recurso
Online Artículo Texto