Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Kathryn McCabe"'
Autor:
Dionnet L. Bhatti, Junghee Jin, Jia Cheng, Kathryn McCabe, Ko-Woon Lee, Clara Berdasco, Yu Young Jeong, Subhash C. Sinha, Yong Kim
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 17 (2024)
The prefrontal cortex (PFC) is a key neural node mediating behavioral responses to stress and the actions of ketamine, a fast-acting antidepressant. The molecular mechanisms underlying these processes, however, are not fully understood. Our recent st
Externí odkaz:
https://doaj.org/article/845b09bf82bf497e8e027498e00a068f
Publikováno v:
POCUS Journal, Vol 5, Iss 1 (2020)
A previously healthy 46-year-old female patient presented to the Emergency Department (ED) with a primary complaint of binocular diplopia worsening over the past 48 hours. Physical exam revealed minor left inferior lid ecchymosis and was significant
Externí odkaz:
https://doaj.org/article/7b7ede80aded486abc47696c48796a1f
Autor:
Lynne McCormack, Linda Swaab, Linda E. Campbell, Emily Freeman, Kathryn McCabe, Kathleen Angkustsiri, Tony J. Simon
Publikováno v:
Journal of Autism and Developmental Disorders. 52:3076-3087
Chromosome 22q11.2 deletion syndrome (22q11DS) is characterised by a complex behavioural phenotype including anxiety, attention-deficit/hyperactivity disorder and psychosis. In the current study, we aimed at improving our understanding of the heterog
Autor:
Joshua Y. Kim, Chunfeng Liu, Rafael A. Calvo, Kathryn McCabe, Silas C. R. Taylor, Björn W. Schuller, Kaihang Wu
Publikováno v:
Lecture Notes in Electrical Engineering ISBN: 9789811955372
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de57bb5d3801c302c4f0e0387dcef126
https://doi.org/10.1007/978-981-19-5538-9_8
https://doi.org/10.1007/978-981-19-5538-9_8
Autor:
Therese van Amelsvoort, Eva W.C. Chow, Marianne Bernadette van den Bree, Paul M. Thompson, Wendy R. Kates, Jacob A. S. Vorstman, Nancy J. Butcher, Julio E Villalon Reina, Clodagh M. Murphy, Eileen Daly, Ania Fiksinski, Donna M. McDonald-McGinn, Raquel E. Gur, Wanda Fremont, David Edmund Johannes Linden, Daqiang Sun, Courtney A. Durdle, Rachel K. Jonas, Hayley Moss, Kosha Ruparel, Tony J. Simon, Nicolas Crossley, J. Eric Schmitt, David R. Roalf, Michael John Owen, Kevin M. Antshel, Sanne Koops, Linda E. Campbell, Beverly S. Emanuel, Anjanibhargavi Ragothaman, Maria Jalbrzikowski, Amy Lin, Kieran C. Murphy, Maria Gudbrandsen, Anne S. Bassett, Ariana Vajdi, T. Blaine Crowley, Dmitry Isaev, Joanne L. Doherty, Boris A. Gutman, Carrie E. Bearden, Kathryn McCabe, Naomi J. Goodrich-Hunsaker, Fidel Vila-Rodriguez, Laura Pacheco-Hansen, Artemis Zavaliangos-Petropulu, Christopher R.K. Ching, Elaine H. Zackai, Geor Bakker, Jennifer K. Forsyth, Adam C. Cunningham, Gabriela M. Repetto, Leila Kushan, Declan G. Murphy, Michael C. Craig
Publikováno v:
American Journal of Psychiatry, 177(7), 589-600. American Psychiatric Publishing, Inc.
The American journal of psychiatry, vol 177, iss 7
Ching, C R K, Gutman, B A, Sun, D, Villalon Reina, J, Ragothaman, A, Isaev, D, Zavaliangos-petropulu, A, Lin, A, Jonas, R K, Kushan, L, Pacheco-hansen, L, Vajdi, A, Forsyth, J K, Jalbrzikowski, M, Bakker, G, Van Amelsvoort, T, Antshel, K M, Fremont, W, Kates, W R, Campbell, L E, Mccabe, K L, Craig, M C, Daly, E, Gudbrandsen, M, Murphy, C M, Murphy, D G, Murphy, K C, Fiksinski, A, Koops, S, Vorstman, J, Crowley, T B, Emanuel, B S, Gur, R E, Mcdonald-mcginn, D M, Roalf, D R, Ruparel, K, Schmitt, J E, Zackai, E H, Durdle, C A, Goodrich-hunsaker, N J, Simon, T J, Bassett, A S, Butcher, N J, Chow, E W C, Vila-rodriguez, F, Cunningham, A, Doherty, J, Linden, D E, Moss, H, Owen, M J, Van Den Bree, M, Crossley, N A, Repetto, G M, Thompson, P M & Bearden, C E 2020, ' Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome : Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness ', American Journal of Psychiatry, vol. 177, no. 7, pp. 589-600 . https://doi.org/10.1176/appi.ajp.2019.19060583
Am J Psychiatry
The American journal of psychiatry, vol 177, iss 7
Ching, C R K, Gutman, B A, Sun, D, Villalon Reina, J, Ragothaman, A, Isaev, D, Zavaliangos-petropulu, A, Lin, A, Jonas, R K, Kushan, L, Pacheco-hansen, L, Vajdi, A, Forsyth, J K, Jalbrzikowski, M, Bakker, G, Van Amelsvoort, T, Antshel, K M, Fremont, W, Kates, W R, Campbell, L E, Mccabe, K L, Craig, M C, Daly, E, Gudbrandsen, M, Murphy, C M, Murphy, D G, Murphy, K C, Fiksinski, A, Koops, S, Vorstman, J, Crowley, T B, Emanuel, B S, Gur, R E, Mcdonald-mcginn, D M, Roalf, D R, Ruparel, K, Schmitt, J E, Zackai, E H, Durdle, C A, Goodrich-hunsaker, N J, Simon, T J, Bassett, A S, Butcher, N J, Chow, E W C, Vila-rodriguez, F, Cunningham, A, Doherty, J, Linden, D E, Moss, H, Owen, M J, Van Den Bree, M, Crossley, N A, Repetto, G M, Thompson, P M & Bearden, C E 2020, ' Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome : Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness ', American Journal of Psychiatry, vol. 177, no. 7, pp. 589-600 . https://doi.org/10.1176/appi.ajp.2019.19060583
Am J Psychiatry
Objective: 22q11.2 deletion syndrome (22q11DS) is among the strongest known genetic risk factors for schizophrenia. Previous studies have reported variable alterations in subcortical brain structures in 22q11DS. To better characterize subcortical alt
Autor:
Carrie E. Bearden, Geor Bakker, Jennifer K. Forsyth, Laura Hansen, Naomi J. Goodrich-Hunsaker, David Edmund Johannes Linden, Eileen Daly, Neda Jahanshad, Wanda Fremont, Conor K. Corbin, Maria Jalbrzikowski, Tony J. Simon, Amy Lin, Marianne Bernadette van den Bree, David R. Roalf, Xiaoping Qu, Kevin M. Antshel, Donna M. McDonald-McGinn, Courtney A. Durdle, Jacob A. S. Vorstman, Raquel E. Gur, Declan G. Murphy, Leila Kushan, Therese van Amelsvoort, Clodagh M. Murphy, Beverly S. Emanuel, Kathryn McCabe, Rachel K. Jonas, Kenia Martínez, J. Eric Schmitt, Christopher R.K. Ching, Hayley Moss, Daqiang Sun, Gary Donohoe, Maria Gudbrandsen, Talia M. Nir, C. Arango, Ariana Vajdi, Sinead Kelly, Julio E. Villalon-Reina, Wendy R. Kates, Kosha Ruparel, Joanne L. Doherty, Michael John Owen, Sanne Koops, Kieran C. Murphy, Michael C. Craig, Ania Fiksinski, Linda E. Campbell, Adam C. Cunningham, Paul M. Thompson, Deydeep Kothapalli
Publikováno v:
Molecular psychiatry, vol 25, iss 11
Villalon-Reina, J E, Martínez, K, Qu, X, Ching, C R K, Nir, T, Kothapalli, D, Corbin, C, Sun, D, Lin, A, Forsyth, J K, Kushan, L, Vajdi, A, Jalbrzikowski, M, Hansen, L, Jonas, R K, Van Amelsvoort, T, Bakker, G, Kates, W R, Antshel, K M, Fremont, W, Campbell, L E, McCabe, K L, Gudbrandsen, C M, Daly, E M, Gudbrandsen, C M, Murphy, C, Murphy, D G, Craig, M, Emanuel, B S, McDonald-McGinn, D M, Vorstman, J A S, Fiksinski, A, Koops, S, Ruparel, K, Roalf, D R, Gur, R E, Schmitt, J E, Simon, T J, Goodrich-hunsaker, N J, Durdle, C A, Doherty, J, Cunningham, A C, van den Bree, M, Linden, D E J, Owen, M J, Moss, H, Kelly, S, Donohoe, G, Murphy, K C, Arango, C, Jahanshad, N, Thompson, P M & Bearden, C E 2019, ' Altered white matter microstructure in 22q11.2 deletion syndrome : a multisite diffusion tensor imaging study ', Molecular Psychiatry . https://doi.org/10.1038/s41380-019-0450-0
Molecular Psychiatry
Molecular Psychiatry, 25(11), 2818-2831. Nature Publishing Group
Villalon-Reina, J E, Martínez, K, Qu, X, Ching, C R K, Nir, T, Kothapalli, D, Corbin, C, Sun, D, Lin, A, Forsyth, J K, Kushan, L, Vajdi, A, Jalbrzikowski, M, Hansen, L, Jonas, R K, Van Amelsvoort, T, Bakker, G, Kates, W R, Antshel, K M, Fremont, W, Campbell, L E, McCabe, K L, Gudbrandsen, C M, Daly, E M, Gudbrandsen, C M, Murphy, C, Murphy, D G, Craig, M, Emanuel, B S, McDonald-McGinn, D M, Vorstman, J A S, Fiksinski, A, Koops, S, Ruparel, K, Roalf, D R, Gur, R E, Schmitt, J E, Simon, T J, Goodrich-hunsaker, N J, Durdle, C A, Doherty, J, Cunningham, A C, van den Bree, M, Linden, D E J, Owen, M J, Moss, H, Kelly, S, Donohoe, G, Murphy, K C, Arango, C, Jahanshad, N, Thompson, P M & Bearden, C E 2019, ' Altered white matter microstructure in 22q11.2 deletion syndrome : a multisite diffusion tensor imaging study ', Molecular Psychiatry . https://doi.org/10.1038/s41380-019-0450-0
Molecular Psychiatry
Molecular Psychiatry, 25(11), 2818-2831. Nature Publishing Group
22q11.2 deletion syndrome (22q11DS)—a neurodevelopmental condition caused by a hemizygous deletion on chromosome 22—is associated with an elevated risk of psychosis and other developmental brain disorders. Prior single-site diffusion magnetic res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dec4bc884702f6509b996d8477f481cc
https://escholarship.org/uc/item/3st981z8
https://escholarship.org/uc/item/3st981z8
Autor:
Therese van Amelsvoort, Maria Jalbrzikowski, Geor Bakker, Jacob A. S. Vorstman, Amy Lin, Donna M. McDonald-McGinn, Raquel E. Gur, Anne S. Bassett, Courtney A. Durdle, Eileen Daly, David Edmund Johannes Linden, Jennifer K. Forsyth, Daqiang Sun, Fidel Vila-Rodriguez, Kathryn McCabe, Laura Hansen, Leila Kushan, J. Eric Schmitt, Carrie E. Bearden, Xiaoping Qu, Clodagh M. Murphy, Kevin M. Antshel, Michael John Owen, Sanne Koops, Beverly S. Emanuel, Kieran C. Murphy, Hayley Moss, Eva W.C. Chow, Julio E. Villalon-Reina, Wendy R. Kates, Nancy J. Butcher, Kosha Ruparel, Naomi J. Goodrich-Hunsaker, Joanne L. Doherty, Rachel K. Jonas, Maria Gudbrandsen, Marianne Bernadette van den Bree, Ariana Vajdi, Christopher R.K. Ching, Declan G. Murphy, Theo G.M. van Erp, David R. Roalf, Ania Fiksinski, Michael C. Craig, Wanda Fremont, Linda E. Campbell, Tony J. Simon, Adam C. Cunningham, Jessica A. Turner, Paul M. Thompson
Publikováno v:
Molecular Psychiatry, 25(8), 1822-1834. Nature Publishing Group
Molecular psychiatry, vol 25, iss 8
Molecular psychiatry
Sun, D, Ching, C R K, Lin, A, Forsyth, J K, Kushan, L, Vajdi, A, Jalbrzikowski, M, Hansen, L, Villalon-reina, J E, Qu, X, Jonas, R K, Van Amelsvoort, T, Bakker, G, Kates, W R, Antshel, K M, Fremont, W, Campbell, L E, Mccabe, K L, Daly, E, Gudbrandsen, M, Murphy, C M, Murphy, D, Craig, M, Vorstman, J, Fiksinski, A, Koops, S, Ruparel, K, Roalf, D R, Gur, R E, Schmitt, J E, Simon, T J, Goodrich-hunsaker, N J, Durdle, C A, Bassett, A S, Chow, E W C, Butcher, N J, Vila-rodriguez, F, Doherty, J, Cunningham, A, Van Den Bree, M B M, Linden, D E J, Moss, H, Owen, M J, Murphy, K C, Mcdonald-mcginn, D M, Emanuel, B, Van Erp, T G M, Turner, J A, Thompson, P M & Bearden, C E 2018, ' Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome : Convergence with idiopathic psychosis and effects of deletion size ', Molecular Psychiatry, vol. 25, no. 8, pp. 1822–1834 . https://doi.org/10.1038/s41380-018-0078-5
Sun, D; Ching, CRK; Lin, A; Forsyth, JK; Kushan, L; Vajdi, A; et al.(2018). Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Molecular Psychiatry, 1-13. doi: 10.1038/s41380-018-0078-5. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/26s9n67w
Molecular psychiatry, vol 25, iss 8
Molecular psychiatry
Sun, D, Ching, C R K, Lin, A, Forsyth, J K, Kushan, L, Vajdi, A, Jalbrzikowski, M, Hansen, L, Villalon-reina, J E, Qu, X, Jonas, R K, Van Amelsvoort, T, Bakker, G, Kates, W R, Antshel, K M, Fremont, W, Campbell, L E, Mccabe, K L, Daly, E, Gudbrandsen, M, Murphy, C M, Murphy, D, Craig, M, Vorstman, J, Fiksinski, A, Koops, S, Ruparel, K, Roalf, D R, Gur, R E, Schmitt, J E, Simon, T J, Goodrich-hunsaker, N J, Durdle, C A, Bassett, A S, Chow, E W C, Butcher, N J, Vila-rodriguez, F, Doherty, J, Cunningham, A, Van Den Bree, M B M, Linden, D E J, Moss, H, Owen, M J, Murphy, K C, Mcdonald-mcginn, D M, Emanuel, B, Van Erp, T G M, Turner, J A, Thompson, P M & Bearden, C E 2018, ' Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome : Convergence with idiopathic psychosis and effects of deletion size ', Molecular Psychiatry, vol. 25, no. 8, pp. 1822–1834 . https://doi.org/10.1038/s41380-018-0078-5
Sun, D; Ching, CRK; Lin, A; Forsyth, JK; Kushan, L; Vajdi, A; et al.(2018). Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Molecular Psychiatry, 1-13. doi: 10.1038/s41380-018-0078-5. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/26s9n67w
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for psychotic illness. Prior studies reported widespread cortical changes in 22q11DS, but were generally underpowered to characterize neuroanatomic abnormal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea36ffa73074e5892b395c1549bccf6b
https://cris.maastrichtuniversity.nl/en/publications/08f62d42-344a-4c68-a3a8-a4ea1ecf7d47
https://cris.maastrichtuniversity.nl/en/publications/08f62d42-344a-4c68-a3a8-a4ea1ecf7d47
Autor:
Richard Duncan, Tao Wang, Carrie E. Bearden, David J. Cutler, Stephen T. Warren, Maria Pontillo, Robert Sean Gallagher, Elemi J. Breetvelt, Tingwei Guo, Nancy J. Butcher, Jennifer G. Mulle, Claudia Ornstein, Claudia Vingerhoets, Clodagh M. Murphy, Ehud Mekori-Domachevsky, Wendy R. Kates, Jacob A. S. Vorstman, Tracy Heung, Joris Vermeesch, Maria Gudbrandsen, Ann Swillen, H. Richard Johnston, Oanh Tran, Marco Armando, Joseph F. Cubells, Raoul Belzeaux, Jeroen Breckpot, Bruno Marino, Tony J. Simon, Harold I. Salmons, Maria Jalbrzikowski, Wanda Fremont, Anna J. Voss, Worrawat Engchuan, Opal Y. Ousley, Stefano Vicari, Jordi Rosell, Sixto García-Miñaur, Declan G. Murphy, Alexander Diacou, Ania Fiksinski, Abraham Weizman, Edward Moss, Stephan Eliez, Miri Carmel, Vandana Shashi, Anne S. Bassett, Ronnie Weinberger, Hayley Moss, Marianne Bernadette van den Bree, Kelly Schoch, Maude Schneider, Linda E. Campbell, Sasja N. Duijff, Eileen Daly, Annick Vogels, Stephen R. Hooper, David Fraguas, Sarah E. Prasad, Chelsea Lowther, Michael John Owen, Frédérique Béna, Gabriela M. Repetto, Eva W.C. Chow, Bernice E. Morrow, Robert J. Sharkus, Celso Arango, Christian R. Marshall, Jasna Raventos-Simic, Jaume Morey-Canyelles, Tiffany Busa, Andrea Jin, James T.R. Walters, Leila Kushan, Wolfram Demaerel, Monica E. Calkins, Jhih Rong Lin, Elaine H. Zackai, Esther D.A. van Duin, Antonio Buzzanca, Corrado Sandini, Kieran C. Murphy, Beverly S. Emanuel, Erik Boot, Maria Niarchou, Nigel Williams, Elfi Vergaelen, Maria Cristina Digilio, Daniele Merico, Karlene Coleman, Gregory A. Costain, Matthew S. Hestand, Peter Holmans, Michael E. Zwick, Michael P. Epstein, Damià H. Suñer, Yingjie Zhao, Marta Unolt, Kathryn McCabe, Aaron M. Holleman, Zhengdong Zhang, Rosemarie Fritsch, Alex V. Kotlar, Elena Michaelovsky, T. Blaine Crowley, Brenna Lilley, Sunny X. Tang, Rens Evers, Ruben C. Gur, Isabelle Cleynen, Flora Tassone, Nicole Philip, Kevin M. Antshel, Koen Devriendt, Antonio F. Pardiñas, Pankaj Chopra, Thomas Monfeuga, Fabio Di Fabio, Therese van Amelsvoort, Aaron Golden, Doron Gothelf, Donna M. McDonald-McGinn, Raquel E. Gur, Daniel E. McGinn
Publikováno v:
Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry (2020)
Molecular psychiatry
Molecular Psychiatry, 26(8), 4496-4510. Nature Publishing Group
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry (2020)
Molecular psychiatry
Molecular Psychiatry, 26(8), 4496-4510. Nature Publishing Group
Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors that contribute to schizophrenia, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4c91788310dcf6c66ef3ac3973170b9
http://hdl.handle.net/20.500.12278/33344
http://hdl.handle.net/20.500.12278/33344
Autor:
Claudia Ornstein, Anne S. Bassett, Matthew S. Hestand, Bruno Marino, Kelly Schoch, Tony J. Simon, Therese van Amelsvoort, Doron Gothelf, Carrie E. Bearden, Elemi J. Breetvelt, Michael P. Epstein, Tiffany Busa, Robert J. Shprintzen, David Cutler, Tao Wang, Leila Kushan-Wells, Donna M. McDonald-McGinn, Raquel E. Gur, Hayley Moss, Esther D. A. van Duin, B Dallapiccola, Joris Vermeesch, Clodagh M. Murphy, Yingjie Zhao, Rens Evers, María Angeles de la Fuente Sanches, Ann Swillen, H. Richard Johnston, Maria Pontillo, Steve Warren, Guido Lattanzi, Michael E. Zwick, Jacob A. S. Vorstman, Jeroen Breckpot, Oanh Tran, Stylianos E. Antonarakis, Stefano Vicari, Andrea Jin, Alexander Diacou, Miri Carmel, Christian R. Marshall, Abraham Weizman, Bernice E. Morrow, Fadi I Musfee, Wendy R. Kates, Michael John Owen, Fabio Di Fabio, Marco Armando, Erik Boot, Claudia Vingerhoets, Elizabeth Goldmuntz, Massimo Biondi, Kieran C. Murphy, Nancy Butcher, Declan G. Murphy, Candice K. Silversides, Isabelle Cleynen, T. Blaine Crowley, Vandana Shashi, Linda E. Campbell, Elaine H. Zackai, Ronnie Weinberger, Sixto García-Miñaur, Marianne Bernadette van den Bree, Fernando García Algas, Damian Heine-Suñer, Tracy Heung, Daniel E. McGinn, Maude Schneider, Stephan Eliez, Marta Unolt, Stephen R. Hooper, Kathryn McCabe, A. J. Agopian, Tingwei Guo, Zhengdong Zhang, Rosemarie Fritsch, Luis Fernández, Beverly S. Emanuel, Elfi Vergaelen, Alejandra Laorden-Nieto, Flora Tassone, Gabriela M. Repetto, Laura E. Mitchell, Antonino Buzzanca, Elena Michaelovsky, M. Cristina Digilio, Nicole Philip
Publikováno v:
American Journal of Human Genetics, 106(1), 26-40. Cell Press
Am J Hum Genet
American Journal of Human Genetics, Vol. 106, No 1 (2020) pp. 26-40
American journal of human genetics, vol 106, iss 1
Am J Hum Genet
American Journal of Human Genetics, Vol. 106, No 1 (2020) pp. 26-40
American journal of human genetics, vol 106, iss 1
The 22q11.2 deletion syndrome (22q11.2DS) results from non-allelic homologous recombination between low-copy repeats termed LCR22. About 60%-70% of individuals with the typical 3 megabase (Mb) deletion from LCR22A-D have congenital heart disease, mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8700304c185800fa1b2e56de201d2874
https://cris.maastrichtuniversity.nl/en/publications/fcebc151-7a92-4dbe-8f36-bd15cb7462bb
https://cris.maastrichtuniversity.nl/en/publications/fcebc151-7a92-4dbe-8f36-bd15cb7462bb
Autor:
Michele Amato, Nicole Tartaglia, Kathryn McCabe, Ling M. Wong, Danielle J Harvey, Abbie Popa, Joshua Cruz, Courtney A. Durdle, Tony J. Simon, Margarita H Cabaral
Publikováno v:
Journal of neurodevelopmental disorders, vol 11, iss 1
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-12 (2019)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-12 (2019)
Journal of Neurodevelopmental Disorders
Objectives Our ability to generate mental representation of magnitude from sensory information affects how we perceive and experience the world. Reduced resolution of the mental representations formed from sensory inputs may generate impairment in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adab0e28f50165cfd8968c3691053b16
https://escholarship.org/uc/item/79q8511r
https://escholarship.org/uc/item/79q8511r