Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Dementia/diagnostic imaging"'
Autor:
Muriel Vélez, Andrea Falconí Paez, Bryan Nicolalde, Camila Esquetini-Vernon, Yana Lara-Taranchenko, Kevin Zambrano, Andrés Caicedo
Publikováno v:
European Neuropsychopharmacology, 61, 91-93. Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e88f9a64e8b01807d2fbe9a62f0b87f
https://cris.maastrichtuniversity.nl/en/publications/54de87e9-249d-4e5a-8bc7-85f553a509ba
https://cris.maastrichtuniversity.nl/en/publications/54de87e9-249d-4e5a-8bc7-85f553a509ba
Autor:
Alexander Drzezga, Silvia Morbelli, Henryk Barthel, Adriaan A. Lammertsma, Ian Law, Elsmarieke van de Giessen, Javier Arbizu, Valentina Garibotto, Gaël Chételat
Publikováno v:
European Journal of Nuclear Medicine and Molecular Imaging, 48(8), 2320-2324. Springer Verlag
European journal of nuclear medicine and molecular imaging, 48(8), 2320-2324. Springer Verlag
European journal of nuclear medicine and molecular imaging 48(8), 2320-2324 (2021). doi:10.1007/s00259-021-05301-7
European journal of nuclear medicine and molecular imaging, Vol. 48, No 8 (2021) pp. 2320-2324
Chételat, G, Arbizu, J, Barthel, H, Garibotto, V, Lammertsma, A A, Law, I, Morbelli, S, van de Giessen, E & Drzezga, A 2021, ' Finding our way through the labyrinth of dementia biomarkers ', European Journal of Nuclear Medicine and Molecular Imaging, vol. 48, no. 8, pp. 2320-2324 . https://doi.org/10.1007/s00259-021-05301-7
European Journal of Nuclear Medicine and Molecular Imaging, 48(8), 2320-2324. SPRINGER
European journal of nuclear medicine and molecular imaging, 48(8), 2320-2324. Springer Verlag
European journal of nuclear medicine and molecular imaging 48(8), 2320-2324 (2021). doi:10.1007/s00259-021-05301-7
European journal of nuclear medicine and molecular imaging, Vol. 48, No 8 (2021) pp. 2320-2324
Chételat, G, Arbizu, J, Barthel, H, Garibotto, V, Lammertsma, A A, Law, I, Morbelli, S, van de Giessen, E & Drzezga, A 2021, ' Finding our way through the labyrinth of dementia biomarkers ', European Journal of Nuclear Medicine and Molecular Imaging, vol. 48, no. 8, pp. 2320-2324 . https://doi.org/10.1007/s00259-021-05301-7
European Journal of Nuclear Medicine and Molecular Imaging, 48(8), 2320-2324. SPRINGER
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39ae9fcaa6ad6fefc2ad3e0b374d32de
https://research.vumc.nl/en/publications/af68e987-5532-4c58-8d2d-7510e00e386f
https://research.vumc.nl/en/publications/af68e987-5532-4c58-8d2d-7510e00e386f
Autor:
Premi, Enrico, Calhoun, Vince D, Galimberti, Daniela, Panman, Jessica, Papma, Janne, Patzig, Maximilian, Pievani, Michela, Prioni, Sara, Prix, Catharina, Rademakers, Rosa, Redaelli, Veronica, Rittman, Tim, Rogaeva, Ekaterina, Sanchez-Valle, Raquel, Rosa-Neto, Pedro, Rossi, Giacomina, Rossor, Martin, Santiago, Beatriz, Scarpini, Elio, Semler, Elisa, Shafei, Rachelle, Shoesmith, Christen, Tábuas-Pereira, Miguel, Tainta, Mikel, Laforce, Robert, Tang-Wai, David, Thomas, David L, Thonberg, Hakan, Timberlake, Carolyn, Tiraboschi, Pietro, Vandamme, Philip, Vandenbulcke, Mathieu, Veldsman, Michele, Verdelho, Ana, Villanua, Jorge, Moreno, Fermin, Warren, Jason, Wilke, Carlo, Zetterberg, Henrik, Zulaica, Miren, Synofzik, Matthis, Graff, Caroline, Masellis, Mario, Tartaglia, Maria Carmela, Rowe, James, Vandenberghe, Rik, Diano, Matteo, Finger, Elizabeth, Tagliavini, Fabrizio, de Mendonça, Alexandre, Santana, Isabel, Butler, Chris, Ducharme, Simon, Gerhard, Alex, Danek, Adrian, Levin, Johannes, Otto, Markus, Gazzina, Stefano, Frisoni, Giovanni, Cappa, Stefano, Sorbi, Sandro, Padovani, Alessandro, Rohrer, Jonathan D, Borroni, Barbara, Genetic FTD Initiative, GENFI, Almeida, Maria Rosario, Anderl-Straub, Sarah, Andersson, Christin, Cosseddu, Maura, Antonell, Anna, Arighi, Andrea, Balasa, Mircea, Barandiaran, Myriam, Bargalló, Nuria, Bartha, Robart, Bender, Benjamin, Benussi, Luisa, Binetti, Giuliano, Black, Sandra, Alberici, Antonella, Bocchetta, Martina, Borrego-Ecija, Sergi, Bras, Jose, Bruffaerts, Rose, Caroppo, Paola, Cash, David, Castelo-Branco, Miguel, Convery, Rhian, Cope, Thomas, de Arriba, María, Archetti, Silvana, Di Fede, Giuseppe, Díaz, Zigor, Dick, Katrina M, Duro, Diana, Fenoglio, Chiara, Ferreira, Carlos, Ferreira, Catarina B, Flanagan, Toby, Fox, Nick, Freedman, Morris, Paternicò, Donata, Fumagalli, Giorgio, Gabilondo, Alazne, Gauthier, Serge, Ghidoni, Roberta, Giaccone, Giorgio, Gorostidi, Ana, Greaves, Caroline, Guerreiro, Rita, Heller, Carolin, Hoegen, Tobias, Gasparotti, Roberto, Indakoetxea, Begoña, Jelic, Vesna, Jiskoot, Lize, Karnath, Hans-Otto, Keren, Ron, Leitão, Maria João, Lladó, Albert, Lombardi, Gemma, Loosli, Sandra, Maruta, Carolina, van Swieten, John, Mead, Simon, Meeter, Lieke, Miltenberger, Gabriel, van Minkelen, Rick, Mitchell, Sara, Nacmias, Benedetta, Neason, Mollie, Nicholas, Jennifer, Öijerstedt, Linn, Olives, Jaume
Publikováno v:
NeuroImage 189, 645-654 (2019). doi:10.1016/j.neuroimage.2019.01.080
NeuroImage, 189, 645-654. Academic Press
Digital.CSIC. Repositorio Institucional del CSIC
instname
NeuroImage, 189, 645-654. Academic Press
Digital.CSIC. Repositorio Institucional del CSIC
instname
© 2019 Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
Frontotemporal Dementia (FTD) is preceded by a long period of subtle brain changes, occurring in
Frontotemporal Dementia (FTD) is preceded by a long period of subtle brain changes, occurring in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1782893dd9dfc2bcea1b493eb41c5fa6
https://doi.org/10.1016/j.neuroimage.2019.01.080
https://doi.org/10.1016/j.neuroimage.2019.01.080
Autor:
Huin, Vincent, Barbier, Mathieu, Bottani, Armand, Lobrinus, Johannes, Clot, Fabienne, Lamari, Foudil, Chat, Laureen, Rucheton, Benoît, Fluchère, Frédérique, Auvin, Stéphane, Myers, Peter, Gelot, Antoinette, Camuzat, Agnès, Caillaud, Catherine, Jornéa, Ludmila, Forlani, Sylvie, Saracino, Dario, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra, Le Ber, Isabelle
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, 2020, 143 (1), pp.303-319. ⟨10.1093/brain/awz377⟩
Brain-A Journal of Neurology, 2020, 143 (1), pp.303-319. ⟨10.1093/brain/awz377⟩
International audience; Homozygous mutations in the progranulin gene (GRN) are associated with neuronal ceroid lipofuscinosis 11 (CLN11), a rare lysosomal-storage disorder characterized by cerebellar ataxia, seizures, retinitis pigmentosa, and cognit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1398::6ccf31a88f1bb53f37d07fa49a3a3ccc
https://www.hal.inserm.fr/inserm-03014481v2/document
https://www.hal.inserm.fr/inserm-03014481v2/document
Autor:
HUIN, Vincent, Barbier, Mathieu, Bottani, Armand, Lobrinus, Johannes, Clot, Fabienne, Lamari, Foudil, Chat, Laureen, Rucheton, Benoît, Fluchère, Frédérique, Auvin, Stéphane, Myers, Peter, Gelot, Antoinette, Camuzat, Agnès, Caillaud, Catherine, Jornéa, Ludmila, Forlani, Sylvie, Saracino, Dario, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra, Le Ber, Isabelle
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2020, 143 (1), pp.303-319. ⟨10.1093/brain/awz377⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2020, 143 (1), pp.303-319. ⟨10.1093/brain/awz377⟩
International audience; Homozygous mutations in the progranulin gene (GRN) are associated with neuronal ceroid lipofuscinosis 11 (CLN11), a rare lysosomal-storage disorder characterized by cerebellar ataxia, seizures, retinitis pigmentosa, and cognit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::03f48b939ec6322f8c0e08f5d5a546c1
https://www.hal.inserm.fr/inserm-03014481v2/document
https://www.hal.inserm.fr/inserm-03014481v2/document
Autor:
Frans R.J. Verhey, Dimo Ivanov, David H. Salat, Lies Clerx, Ed H.B.M. Gronenschild, Whitney M. Freeze, Heidi I.L. Jacobs, Joost M. Riphagen, Pauline Aalten
Publikováno v:
Neurobiology of Aging, 68, 48-58. Elsevier Science
The underlying pathology of white matter signal abnormalities (WMSAs) is heterogeneous and may vary dependent on the magnetic resonance imaging contrast used to define them. We investigated differences in white matter diffusivity as an indicator for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c495d558fc454c6c74d786b1ea1e73f0
https://doi.org/10.1016/j.neurobiolaging.2018.03.029
https://doi.org/10.1016/j.neurobiolaging.2018.03.029
Autor:
Antoinette Gelot, Alexis Brice, Agnès Camuzat, Benoit Rucheton, Laureen Chat, Dario Saracino, Frédérique Fluchère, Johannes Alexander Lobrinus, Fabienne Clot, Sylvie Forlani, Peter Myers, Alexandra Durr, Ludmila Jornea, Isabelle Le Ber, Vincent Huin, Foudil Lamari, Mathieu Barbier, Armand Bottani, Catherine Caillaud, Stéphane Auvin, Charles Duyckaerts
Publikováno v:
Brain, Vol. 143, No 1 (2020) pp. 303-319
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2020, 143 (1), pp.303-319. ⟨10.1093/brain/awz377⟩
Brain-A Journal of Neurology, 2020, 143 (1), pp.303-319. ⟨10.1093/brain/awz377⟩
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2020, 143 (1), pp.303-319. ⟨10.1093/brain/awz377⟩
Brain-A Journal of Neurology, 2020, 143 (1), pp.303-319. ⟨10.1093/brain/awz377⟩
Homozygous mutations in the progranulin gene (GRN) are associated with neuronal ceroid lipofuscinosis 11 (CLN11), a rare lysosomal-storage disorder characterized by cerebellar ataxia, seizures, retinitis pigmentosa, and cognitive disorders, usually b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2606313088e1f00ce84d434e32646b88
https://pubmed.ncbi.nlm.nih.gov/33844830
https://pubmed.ncbi.nlm.nih.gov/33844830
Autor:
Guillaume Martin-Blondel, Marie Benaiteau, Florian Perez, Hélène Mirabel, Laura Guerrier, Emilie Rigal, Jérémie Pariente, Eve Salleles, El Hadji Makhtar Ba
Publikováno v:
Journal of Neuropsychiatry and Clinical Neurosciences
Journal of Neuropsychiatry and Clinical Neurosciences, 2019, 31 (3), pp.268-271. ⟨10.1176/appi.neuropsych.18050100⟩
Journal of Neuropsychiatry and Clinical Neurosciences, 2019, 31 (3), pp.268-271. ⟨10.1176/appi.neuropsych.18050100⟩
International audience; Subacute cognitive disorders are frequently encountered in clinical practice, and many pathologies result in such presentations. Consequently, prompt and precise etiologic diagnosis is necessary because, in some cases, introdu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e89cdc135e88c932a506905c89024c9d
https://doi.org/10.1176/appi.neuropsych.18050100
https://doi.org/10.1176/appi.neuropsych.18050100
Autor:
Federica Agosta, Javier Arbizu, Peter J. Nestor, Alexander Drzezga, Stefania Orini, Daniele Altomare, Cristina Festari, Femke H. Bouwman, Flavio Nobili, Koen Van Laere, Zuzana Walker, Marina Boccardi
Publikováno v:
European Journal of Nuclear Medicine and Molecular Imaging, Vol. 45, No 9 (2018) pp. 1557-1566
For the EANM-EAN Task Force for the Prescription of FDG-PET for Dementing Neurodegenerative Disorders 2018, ' Automated assessment of FDG-PET for differential diagnosis in patients with neurodegenerative disorders ', European Journal of Nuclear Medicine and Molecular Imaging, vol. 45, no. 9, pp. 1557-1566 . https://doi.org/10.1007/s00259-018-4030-3
European journal of nuclear medicine and molecular imaging 45(9), 1557-1566 (2018). doi:10.1007/s00259-018-4030-3
For the EANM-EAN Task Force for the Prescription of FDG-PET for Dementing Neurodegenerative Disorders 2018, ' Automated assessment of FDG-PET for differential diagnosis in patients with neurodegenerative disorders ', European Journal of Nuclear Medicine and Molecular Imaging, vol. 45, no. 9, pp. 1557-1566 . https://doi.org/10.1007/s00259-018-4030-3
European journal of nuclear medicine and molecular imaging 45(9), 1557-1566 (2018). doi:10.1007/s00259-018-4030-3
PURPOSE: To review literature until November 2015 and reach a consensus on whether automatic semi-quantification of brain FDG-PET is useful in the clinical setting for neurodegenerative disorders. METHODS: A literature search was conducted in Medline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2855427d0b31d73b1317e803367b92eb
https://archive-ouverte.unige.ch/unige:114049
https://archive-ouverte.unige.ch/unige:114049
Autor:
Valentina Garibotto, Maura Cosseddu, Marinella Turla, Barbara Borroni, Barbara Paghera, Alessandro Padovani, Enrico Premi, Stefano Gazzina, Mario Grassi
Publikováno v:
Behavioural Brain Research, Vol. 245 (2013) pp. 58-62
a b s t r a c t Background: The brain reserve hypothesis posits that there are individual differences in the ability to cope with brain pathology, and that brain damage extent and clinical symptoms are not tightly linked. If cognitive reserve hypothe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2af987a73619b0d222633e63c617e3b7
https://doi.org/10.1016/j.bbr.2013.01.030
https://doi.org/10.1016/j.bbr.2013.01.030