Results 11 to 20 of about 282,431 (259)
Stratified medicine for mental disorders [PDF]
, 2014 There is recognition that biomedical research into the causes of mental disorders and their treatment needs to adopt new approaches to research. Novel biomedical techniques have advanced our understanding of how the brain develops and is shaped by ...Meyer-Lindenberg, Andreas, Stephani, Klaas E., Haro, J.M., Frith, Chris D., de Kloet ER, Lewis, S, Vieta E, Ciccocioppo, R., Flor, Herta, Vieta, Eduard, Schumann, G., Brown, Verity J., Nutt, DJ, Kirschbaum, C, Cools R, de Kloet, E Ronald, Roiser, JP., Müller, Christian P, Holte, A, Müller, W.E., Martinot JL, Walker-Tilley, TR, Nutt, D., Heinz, A., Bitter I, Martinot, J-L, Müller, Walter E., Roiser, JP, Wykes T, Walker Tilley TR, Lesch, K., Pessiglione, M, Lewis, Shon, Lesch, K.P., Wittchen HU, Maria Haro, J., Walker-Tilley, Tom R, Mueller, Walter E., Oedegaard, K.J., Haro JM, Sandi, C, Robbins, Trevor W, Fleischhacker, W, Holte, A., Maier, Wolfgang, Oedegaard, K., Robbins, T.W., Buitelaar J, Preuss, Ulrich W., Perugi, G, Flor, H., Rybakowski, Janusz, Persico, A., Binder, Elisabeth B., Roiser, J., de Kloet, E.R., Müller, C.P., Haro, Josep Maria, Rossini, Paolo M., Schumann, Gunter, Johnsen, Erik, Roiser, Jonathan P, Schumann, G, Sandi, Carmen, Ciccocioppo R, Escera, C., Oedegaard, KJ, Nutt, David J, Binder, Elizabeth B., Perugi, Giulio, Brown, Verity J, Martinot, JL., Lewis, S., Wittchen, H., Müller, Walter E, Fleischhacker, Wolfgang W., Flor H, Cools, R., Lewis S, Rossini, P.M., Rybakowski, Janusz K., Stephan, K.E., Escera, Carles, Lesch, K.-P., Wittchen, Hans Ulrich, Klingberg, Torkel, Maier, W., Wykes, T., Lesch KP, Walker-Tilley, Tom R., Walker-Tilley, T., Heinz A, Holte, Arne, van der Wee N, Wittchen, HU, Stephan KE, Meyer-Lindenberg A, Meyer-Lindenberg, A., Maier W, Binder EB, Oedegaard, Ketil J, van der Wee, N., Nutt, David J., Undurraga, J., Pessiglione, M., Binder, Elisabeth B, Lewis, Shon; id_orcid, et al, Wittchen, Hans-Ulrich, Flor, H, Nutt DJ, Pessiglione, Mathias, Mueller, CP, Lesch, KP., Ciccocioppo, R, Heinz, A, Binder, E.B., Frith, C.D., Buitelaar, Jan, Oedegaard KJ, Nutt, D.J., Rybakowski, J.K., CICCOCIOPPO, Roberto, Rybakowski, J., Walker-Tilley TR, Johnsen E, Perugi, G., Rybakowski, Janusz K, Mueller, C., Brown, V.J., Lesch, K-P, Roiser, Jonathan P., Persico, Antonio, Johnsen, E, Rybakowski, JK, Martinot, J.L., van der Wee, Nic, Wykes, Til, Preuss, U.W., Wittchen, H.U., Müller, CP., Preuss, U., Rybakowski JK, Sandi C, M?ller CP, Stephan, K., Brown VJ, de Kloet, E. Ronald, Rossini PM, Rybakowski, JK., Wee, N. van der, Pessiglione M, Rossini, PM., Wittchen, HU., Roiser JP, Cools, Roshan, Persico, A, Stephan, KE, Rossini, Paolo M, Wykes, T, Frith, C., Mueller, W., Kloet, E.R. de, Klingberg, T, Maria Haro, Josep, Undurraga J, Mann, K, Robbins TW, Maier, W, Frith CD, Preuss, UW, Buitelaar, J.K., Buitelaar, J., Mann K, van der Wee, N, Buitelaar, J, Sandi, C., Muller WE, Preuss, Ulrich W, Meyer-Lindenberg, A, Müller, WE., Escera, C, Stephan, Klaas E., Perugi, Guilio, de Kloet, ER, Oedegaard, Ketil J., de Kloet, E. R., Escera C, Kirschbaum, Clemens, Wee, N.J.A. van der, Bitter, István, Stephan, KE., Bitter, I., Klingberg T, Mueller, WE, Meyer Lindenberg A, Robbins, Trevor W., Binder, E., Lesch, Klaus-Peter, Johnsen, E., Holte A, de Kloet, E., Cools, R, Undurraga, J, Frith, CD, Undurraga, Juan, Nutt, DJ., Martinot, J., Martinot, J.-L., Robbins, T., Maria Haro, J, Rossini, Paolo Maria, Mann, Karl, Schumann G, Frith, Chris D, Binder, EB, Stephan, Klaas E, Fleischhacker, W., Rossini, PM, Martinot, Jean-Luc, Mueller, Christian P., Bitter, I, Walker-Tilley, T.R., Müller, Christian P., Klingberg, T., Heinz, Andreas, Brown, VJ, Persico A, Brown, V., Kirschbaum, C., Muller CP, Vieta, E., Fleischhacker W, Preuss, UW., M?ller WE, Robbins, TW, Rossini, P., Mann, K., Vieta, E, Kirschbaum C, Wykes, Til; id_orcid, Roiser, J.P., Fleischhacker, Wolfgang, Haro, JM., Perugi G, Preuss UW +245 morecore +1 more sourceSocial cognition in Williams Syndrome: genotype/phenotype insights from partial deletion patients [PDF]
, 2012 Identifying genotype/phenotype relations in human social cognition has been enhanced by the study of Williams syndrome (WS). Indeed, individuals with WS present with a particularly strong social drive, and researchers have sought to link deleted genes in Kay eMetcalfe, Metcalfe, K., Annette Karmiloff-Smith, Senju, Atsushi, Peter Turnpenny, Wu, Racehl, Longhi, Elena, Happé, Francesca, Kay Metcalfe, Sansbury, F., Hannah Broadbent, Longhi, E, Metcalfe, Kay, Farran, EK, D'Souza, D, Happé, F., Turnpenny, Peter, Annette eKarmiloff-Smith, Wu, Rachel, Elena eLonghi, Longhi, E., Sansbury, Francis, Francesca eHappé, D'Souza, Dean, Farran, Emily, Elena Longhi, Tassabehji, M., Emily K. Farran, Turnpenny, P., Metcalfe, K, Tassabehji, May, Karmiloff-Smith, A, Dean eD'Souza, Broadbent, H., Broadbent, Hannah, Tassabehji, M, Atsushi Senju, Broadbent, H, Francis eSansbury, Rachel Wu, Wu, R, Peter eTurnpenny, May eTassabehji, Happé, F, Farran, E.K., Atsushi eSenju, Francis Sansbury, Turnpenny, P, Dean D’Souza, Francesca Happé, Senju, A, Hannah eBroadbent, Rachel eWu, Sansbury, F, May Tassabehji, Karmiloff-Smith, Annette, Farran, Emily K +56 morecore +1 more sourceVascular Cognitive Disorder
Seminars in Neurology, 2019 AbstractThe term vascular cognitive disorder (VCD) refers to a heterogeneous group of disorders in which the primary feature is cognitive impairment attributable to cerebrovascular disease (CVD). This includes not only vascular dementia (VaD) but also cognitive impairment of insufficient severity to meet diagnostic criteria for dementia.Paradise, Matt, Sachdev, PSopenaire +3 more sourcesInertial-Magnetic Sensors for Assessing Spatial Cognition in Infants [PDF]
, 2011 This paper describes a novel approach to the
assessment of spatial cognition in children. In particular we
present a wireless instrumented toy embedding magneto-inertial
sensors for orientation tracking, specifically developed to assess
the ability to ...Campolo, Domenico, Domenico Campolo, Eugenio Guglielmelli, Formica, Domenico, Guglielmelli, Eugenio, Giuseppina Schiavone, Keller, Flavio, Flavio Keller, Domenico Formica, Schiavone, Giuseppina, Taffoni, Fabrizio, Fabrizio Taffoni +11 morecore +1 more sourceCognitions and Emotions in Eating Disorders [PDF]
, 2010 The cognitive model of eating disorders (EDs) states that the processing of external and internal stimuli might be biased in mental disorders. These biases, or cognitive errors, systematically distort the individual's experiences and, in that way, maintains the eating disorder.Siep, N., Jansen, A., Havermans, R., Roefs, A. +3 moreopenaire +3 more sourcesNeurocognitive phenomics: examining the genetic basis of cognitive abilities [PDF]
, 2013 Cognitive deficits are core to the disability associated with many psychiatric disorders. Both variation in cognition and psychiatric risk show substantial heritability, with overlapping genetic variants contributing to both.D. C. Glahn, Malhotra, A. K., I. J. Deary, Glahn, D. C., Deary, I. J., Donohoe, G., G. Donohoe, K. E. Burdick, A. K. Malhotra, Burdick, K. E. +9 morecore +1 more sourceHospitalization Through Families’ Eyes: Comparing Inpatient Care Quality for Children With Sickle Cell Disease and Cystic Fibrosis in Canada
Pediatric Blood &Cancer, EarlyView.ABSTRACT Background
Sickle cell disease (SCD) is a chronic, inherited hemoglobinopathy that requires frequent hospitalization for disease‐related complications. Canadian data on inpatient care is limited. This study compared caregiver‐reported hospital experiences of children with SCD to those with cystic fibrosis (CF), a chronic, autosomal recessive ...Hailey M. Zwicker, Kyle Kemp, Perri Tutelman, Sharon H. J. Hou, Paul Fairie, Maria Santana, Gregory M. T. Guilcher, Taryn Fay‐McClymont, Glenda Bendiak, Wendy Pelletier, Nicola Wright, Fiona Schulte +11 morewiley +1 more sourceIncreased Risk of Sarcomas in Children With Congenital Anomalies: Findings From the Genetic Overlap Between Anomalies and Cancer in Kids (GOBACK) Registry Linkage Study
Pediatric Blood &Cancer, EarlyView.ABSTRACT Background
Pediatric sarcomas are a heterogeneous group of tumors that contribute disproportionately to cancer mortality in children. Although congenital anomalies are among the strongest known risk factors for childhood cancer, the risk of specific sarcoma subtypes among affected individuals has not yet been thoroughly evaluated. Procedure
We Russ Wolters, Ji Yun Tark, Tiffany M. Chambers, Tania A. Desrosiers, Michael E. Scheurer, Charles Shumate, Wendy N. Nembhard, Mahsa M. Yazdy, Eirini Nestoridi, Amanda E. Janitz, Jean Paul Tanner, Russell S. Kirby, Jason L. Salemi, Yao Yu, Chad D. Huff, Sharon E. Plon, Philip J. Lupo, Jeremy M. Schraw +17 morewiley +1 more source
