Zobrazeno 1 - 10
of 41
pro vyhledávání: '"BA, Brodmann area"'
Akademický článek
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Autor:
Geraint Rees, Parashkev Nachev, Robert Gray, Hans Rolf Jäger, Tianbo Xu, Amy Nelson, Jorge Cardoso, Sebastien Ourselin, Anna K. Bonkhoff, Ashwani Jha
Publikováno v:
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior
Cognitive and behavioural outcomes in stroke reflect the interaction between two complex anatomically-distributed patterns: the functional organization of the brain and the structural distribution of ischaemic injury. Conventional outcome models—fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c45c7b9a2ae495f37fa113b6c0787dd
http://europepmc.org/articles/PMC8650827
http://europepmc.org/articles/PMC8650827
Autor:
Stephan Wolpert, Lukas Rüttiger, Dennis Zelle, Moritz Walter, John Thiericke, B Hofmeier, Christoph Braun, Ebrahim Saad Aldamer, Marlies Knipper, Uwe Klose
Publikováno v:
NeuroImage : Clinical
NeuroImage: Clinical, Vol 20, Iss, Pp 637-649 (2018)
NeuroImage: Clinical, Vol 20, Iss, Pp 637-649 (2018)
The exact neurophysiological basis of chronic tinnitus, which affects 10-15% of the population, remains unknown and is controversial at many levels. It is an open question whether phantom sound perception results from increased central neural gain or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57784b61b3c178889a1875ae03668571
https://doi.org/10.1016/j.nicl.2018.08.029
https://doi.org/10.1016/j.nicl.2018.08.029
Autor:
David J. Irwin, James C. Gee, Vivianna M. Van Deerlin, Christopher Olm, Philip A. Cook, Murray Grossman, Corey T. McMillan
Publikováno v:
NeuroImage : Clinical
NeuroImage: Clinical, Vol 19, Iss, Pp 497-506 (2018)
NeuroImage: Clinical, Vol 19, Iss, Pp 497-506 (2018)
Introduction Mutations in the progranulin (GRN) gene are a major source of inherited frontotemporal degeneration (FTD) spectrum disorders associated with TDP-43 proteinopathy. We use structural MRI to identify regions of baseline differences and long
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d85a4b488666bff120c93271c00fd7f
https://doi.org/10.1016/j.nicl.2018.05.017
https://doi.org/10.1016/j.nicl.2018.05.017
Akademický článek
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Publikováno v:
Muñoz-Neira, C, Tedde, A, Coulthard, E J, Thai, N J & Pennington, C M 2019, ' Neural correlates of altered insight in frontotemporal dementia : a systematic review ', NeuroImage: Clinical, vol. 24, 102066 . https://doi.org/10.1016/j.nicl.2019.102066
NeuroImage : Clinical
Muñoz-Neira, C, Tedde, A, Coulthard, E, Thai, N J & Pennington, C 2019, ' Neural correlates of altered insight in frontotemporal dementia: a systematic review ', NeuroImage: Clinical, vol. 24, pp. 102066 . https://doi.org/10.1016/j.nicl.2019.102066
NeuroImage: Clinical, Vol 24, Iss, Pp-(2019)
NeuroImage : Clinical
Muñoz-Neira, C, Tedde, A, Coulthard, E, Thai, N J & Pennington, C 2019, ' Neural correlates of altered insight in frontotemporal dementia: a systematic review ', NeuroImage: Clinical, vol. 24, pp. 102066 . https://doi.org/10.1016/j.nicl.2019.102066
NeuroImage: Clinical, Vol 24, Iss, Pp-(2019)
Highlights • Fractionating insight into objects aids its neuroanatomical exploration in dementia. • Distinctive neural correlates seem to underpin different insight objects in FTD. • Altered insight into disease/health condition mostly involves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0089015e0250327e8f25ded62dfd45c
https://hdl.handle.net/1983/8a977835-b0a2-4cc5-9b1b-7ac6db21ed67
https://hdl.handle.net/1983/8a977835-b0a2-4cc5-9b1b-7ac6db21ed67
Autor:
Ana Saitovitch, Jennifer Boisgontier, Elza Rechtman, Ludovic Fillon, David Grevent, Odile Boute, Elise Schaefer, Elodie Sanchez, Damien Sanlaville, Natacha Lehman, Laurence Faivre, David Geneviève, Vincent Gatinois, Nathalie Boddaert, Jean Marc Tacchella, Kim-Hanh Le Quang Sang, Marlène Rio, M. Zilbovicius, Hervé Lemaitre, Stanislas Lyonnet, Guilaine Boursier, Geneviève Baujat
Publikováno v:
Neuroimage-Clinical
Neuroimage-Clinical, Elsevier, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩
NeuroImage: Clinical, Vol 21, Iss, Pp-(2019)
NeuroImage : Clinical
Neuroimage-Clinical, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩
Neuroimage-Clinical, Elsevier, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩
NeuroImage: Clinical, Vol 21, Iss, Pp-(2019)
NeuroImage : Clinical
Neuroimage-Clinical, 2019, 21, pp.101610. ⟨10.1016/j.nicl.2018.11.020⟩
Kabuki syndrome (KS) is a rare congenital disorder (1/32000 births) characterized by distinctive facial features, intellectual disability, short stature, and dermatoglyphic and skeletal abnormalities. In the last decade, mutations in KMT2D and KDM6A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb98025bcde8087c27465afe3e28b583
https://hal.umontpellier.fr/hal-02573243/file/IRMB_156_main.pdf
https://hal.umontpellier.fr/hal-02573243/file/IRMB_156_main.pdf
Autor:
Laura R. Ment, Karen C. Schneider, Dustin Scheinost, Megan Rowlands, Cheryl Lacadie, Fangyong Li, Betty R. Vohr, R. Todd Constable
Publikováno v:
NeuroImage: Clinical, Vol 11, Iss C, Pp 149-157 (2016)
NeuroImage : Clinical
NeuroImage : Clinical
Background Preterm (PT) children show early cognitive and language deficits and display altered cortical connectivity for language compared to term (T) children. Developmentally, functional connectivity networks become more segregated and integrated,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b98118299e94c4cca27db417472a8ec
http://www.sciencedirect.com/science/article/pii/S2213158216300158
http://www.sciencedirect.com/science/article/pii/S2213158216300158
Autor:
Katherine Schiller, Megan Battles Parsons, Michael P. Cannito, Asim F. Choudhri, Wei Zhang, Mark S. LeDoux, Crystal G. Franklin, Peter T. Fox, Shalini Narayana
Publikováno v:
NeuroImage: Clinical, Vol 27, Iss, Pp 102285-(2020)
NeuroImage : Clinical
NeuroImage : Clinical
Highlights • Developed and validated an overt continuous speech paradigm for use in fMRI. • The speech paradigm successfully identified the neural circuit of speech production. • The speech paradigm is effective in mapping disordered motor spee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12b5539a2376f3c0a81b31c54e4eb8ed
https://doi.org/10.1016/j.nicl.2020.102285
https://doi.org/10.1016/j.nicl.2020.102285
Autor:
Baroukh M. Assael, Giada Zoccatelli, Franco Alessandrini, Sandra Perobelli, Alberto Beltramello, Elena Nicolis, Marco Cipolli
Publikováno v:
NeuroImage : Clinical
NeuroImage: Clinical, Vol 7, Iss C, Pp 721-731 (2015)
NeuroImage: Clinical, Vol 7, Iss C, Pp 721-731 (2015)
Shwachman–Diamond syndrome is a rare recessive genetic disease caused by mutations in SBDS gene, at chromosome 7q11. Phenotypically, the syndrome is characterized by exocrine pancreatic insufficiency, bone marrow dysfunction, skeletal dysplasia and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26ad6e4e3b4c7c00015c124b7af7a270
http://europepmc.org/articles/PMC4375735
http://europepmc.org/articles/PMC4375735