Zobrazeno 1 - 10
of 21
pro vyhledávání: '"genetics [Progranulins]"'
Autor:
Foster, Phoebe H, Russell, Lucy L, Moreno, Fermin, Meeter, Lieke, Miltenberger, Gabriel, van Minkelen, Rick, Mitchell, Sara, Moore, Katrina, Nacmias, Benedetta, Nelson, Annabel, Öijerstedt, Linn, Olives, Jaume, Ourselin, Sebastien, Sanchez-Valle, Raquel, Padovani, Alessandro, Panman, Jessica, Papma, Janne M, Pijnenburg, Yolande, Polito, Cristina, Premi, Enrico, Prioni, Sara, Prix, Catharina, Rademakers, Rosa, Redaelli, Veronica, Laforce, Robert, Rinaldi, Daisy, Rittman, Tim, Rogaeva, Ekaterina, Rollin, Adeline, Rosa-Neto, Pedro, Rossi, Giacomina, Rossor, Martin, Santiago, Beatriz, Saracino, Dario, Sayah, Sabrina, Graff, Caroline, Scarpini, Elio, Schönecker, Sonja, Seelaar, Harro, Semler, Elisa, Shafei, Rachelle, Shoesmith, Christen, Swift, Imogen, Tábuas-Pereira, Miguel, Tainta, Mikel, Taipa, Ricardo, Masellis, Mario, Tang-Wai, David, Thomas, David L, Thompson, Paul, Thonberg, Hakan, Timberlake, Carolyn, Tiraboschi, Pietro, Todd, Emily, Van Damme, Philip, Vandenbulcke, Mathieu, Veldsman, Michele, Tartaglia, Carmela, Verdelho, Ana, Villanua, Jorge, Warren, Jason, Wilke, Carlo, Woollacott, Ione, Wlasich, Elisabeth, Zetterberg, Henrik, Zulaica, Miren, Rowe, James B, Borroni, Barbara, Finger, Elizabeth, Synofzik, Matthis, Peakman, Georgia, Galimberti, Daniela, Vandenberghe, Rik, de Mendonça, Alexandre, Butler, Chris R, Gerhard, Alex, Ducharme, Simon, Le Ber, Isabelle, Tagliavini, Fabrizio, Santana, Isabel, Pasquier, Florence, Convery, Rhian S, Levin, Johannes, Danek, Adrian, Otto, Markus, Sorbi, Sandro, Rohrer, Jonathan D, Initiative, Genetic FTD, Afonso, Sónia, Almeida, Maria Rosario, Anderl-Straub, Sarah, Andersson, Christin, Bouzigues, Arabella, Antonell, Anna, Archetti, Silvana, Arighi, Andrea, Balasa, Mircea, Barandiaran, Myriam, Bargalló, Nuria, Bartha, Robart, Bender, Benjamin, Benussi, Alberto, Bertoux, Maxime, Greaves, Caroline V, Bertrand, Anne, Bessi, Valentina, Black, Sandra, Borrego-Ecija, Sergi, Bras, Jose, Brice, Alexis, Bruffaerts, Rose, Camuzat, Agnès, Cañada, Marta, Cantoni, Valentina, Bocchetta, Martina, Caroppo, Paola, Cash, David, Castelo-Branco, Miguel, Colliot, Olivier, Cope, Thomas, Deramecourt, Vincent, de Arriba, María, Di Fede, Giuseppe, Díez, Alina, Duro, Diana, Cash, David M, Fenoglio, Chiara, Ferrari, Camilla, Ferreira, Catarina B, Fox, Nick, Freedman, Morris, Fumagalli, Giorgio, Funkiewiez, Aurélie, Gabilondo, Alazne, Gasparotti, Roberto, Gauthier, Serge, van Swieten, John C, Gazzina, Stefano, Giaccone, Giorgio, Gorostidi, Ana, Greaves, Caroline, Guerreiro, Rita, Heller, Carolin, Hoegen, Tobias, Indakoetxea, Begoña, Jelic, Vesna, Karnath, Hans Otto, Jiskoot, Lize C, Keren, Ron, Kuchcinski, Gregory, Langheinrich, Tobias, Lebouvier, Thibaud, Leitão, Maria João, Lladó, Albert, Lombardi, Gemma, Loosli, Sandra, Maruta, Carolina, Mead, Simon
Publikováno v:
the Genetic FTD Initiative (GENFI) 2022, ' Examining empathy deficits across familial forms of frontotemporal dementia within the GENFI cohort ', Cortex, vol. 150, pp. 12-28 . https://doi.org/10.1016/j.cortex.2022.01.012
Neuroscience Institute Publications
Cortex 150, 12-28 (2022). doi:10.1016/j.cortex.2022.01.012
Cortex, 150, 12-28. Masson SpA
Neuroscience Institute Publications
Cortex 150, 12-28 (2022). doi:10.1016/j.cortex.2022.01.012
Cortex, 150, 12-28. Masson SpA
© 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).
Background: Reduced empathy is a common symptom in frontotemporal dementia (FTD). Although e
Background: Reduced empathy is a common symptom in frontotemporal dementia (FTD). Although e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fcb8bde2e6d9f515b9bfd97df43f61f
https://doi.org/10.1016/j.cortex.2022.01.012
https://doi.org/10.1016/j.cortex.2022.01.012
Autor:
Premi, Enrico, Costa, Tommaso, Moreno, Fermin, Panman, Jessica, Papma, Janne, Pievani, Michela, Pijnenburg, Yolande, Polito, Cristina, Prioni, Sara, Prix, Catharina, Rademakers As London Ontario Geneticist, Rosa, Redaelli, Veronica, Rittman, Tim, Santana, Isabel, Rogaeva, Ekaterina, Rosa-Neto, Pedro, Rossi, Giacomina, Rossor, Martin, Santiago, Beatriz, Scarpini, Elio, Schönecker, Sonja, Semler, Elisa, Shafei, Rachelle, Shoesmith, Christen, Laforce, Robert, Tábuas-Pereira, Miguel, Tainta, Mikel, Taipa, Ricardo, Tang-Wai, David, L Thomas, David, Thompson, Paul, Thonberg, Hakan, Timberlake, Carolyn, Tiraboschi, Pietro, Van Damme, Philip, Ducharme, Simon, Vandenbulcke, Mathieu, Veldsman, Michele, Verdelho, Ana, Villanua, Jorge, Warren, Jason, Wilke, Carlo, Woollacott, Ione, Wlasich, Elisabeth, Zetterberg, Henrik, Zulaica, Miren, Graff, Caroline, Galimberti, Daniela, Masellis, Mario, Tartaglia, Carmela, Rowe, James B, Finger, Elizabeth, Gazzina, Stefano, Tagliavini, Fabrizio, de Mendonça, Alexandre, Vandenberghe, Rik, Gerhard, Alexander, Butler, Chris R, Danek, Adrian, Synofzik, Matthis, Levin, Johannes, Otto, Markus, Ghidoni, Roberta, Benussi, Alberto, Frisoni, Giovanni B, Sorbi, Sandro, Peakman, Georgia, Todd, Emily, Bocchetta, Martina, Rohrer, Johnathan D, Borroni, Barbara, Members, GENFI Consortium, Afonso, Sónia, Rosario Almeida, Maria, Cauda, Franco, Anderl-Straub, Sarah, Andersson, Christin, Antonell, Anna, Arighi, Andrea, Balasa, Mircea, Barandiaran, Myriam, Bargalló, Nuria, Bartha, Robart, Bender, Benjamin, Benussi, Luisa, Gasparotti, Roberto, Bessi, Valentina, Binetti, Giuliano, Black, Sandra, Borrego-Ecija, Sergi, Bras, Jose, Bruffaerts, Rose, Caroppo, Paola, Cash, David, Castelo-Branco, Miguel, Convery, Rhian, Archetti, Silvana, Cope, Thomas, de Arriba, María, Di Fede, Giuseppe, Díaz, Zigor, Duro, Diana, Fenoglio, Chiara, Ferrari, Camilla, B Ferreira, Catarina, Fox, Nick, Freedman, Morris, Alberici, Antonella, Fumagalli, Giorgio, Gabilondo, Alazne, Gauthier, Serge, Giaccone, Giorgio, Gorostidi, Ana, Greaves, Caroline, Guerreiro, Rita, Heller, Carolin, Hoegen, Tobias, Indakoetxea, Begoña, van Swieten, John C, Jelic, Vesna, Jiskoot, Lize, Karnath, Hans Otto, Keren, Ron, Langheinrich, Tobias, João Leitão, Maria, Lladó, Albert, Lombardi, Gemma, Loosli, Sandra, Maruta, Carolina, Sanchez-Valle, Raquel, Mead, Simon, Meeter, Lieke, Miltenberger, Gabriel, van Minkelen, Rick, Mitchell, Sara, Moore, Katrina, Nacmias, Benedetta, Nicholas, Jennifer, Öijerstedt, Linn, Olives, Jaume
Publikováno v:
Journal of Alzheimer's Disease, 86(1), 205-218. IOS Press BV
Neuroscience Institute Publications
Journal of Alzheimer's disease 86(1), 205-218 (2022). doi:10.3233/JAD-215447
Neuroscience Institute Publications
Journal of Alzheimer's disease 86(1), 205-218 (2022). doi:10.3233/JAD-215447
Background:Magnetic resonance imaging (MRI) measures may be used as outcome markers in frontotemporal dementia (FTD). Objectives:To predict MRI cortical thickness (CT) at follow-up at the single subject level, using brain MRI acquired at baseline in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::815e0a4f9ebcf6d5142f8900ca6d705a
https://doi.org/10.3233/jad-215447
https://doi.org/10.3233/jad-215447
Autor:
Tipton, Philip Wade, Deutschlaender, Angela B, Savica, Rodolfo, Heckman, Michael G, Brushaber, Danielle E, Dickerson, Bradford C, Gavrilova, Ralitza H, Geschwind, Daniel H, Ghoshal, Nupur, Graff-Radford, Jonathan, Graff-Radford, Neill R, Grossman, Murray, Hsiung, Ging-Yuek R, Huey, Edward D, Irwin, David John, Jones, David T, Knopman, David S, McGinnis, Scott M, Rademakers, Rosa, Ramos, Eliana Marisa, Forsberg, Leah K, Heuer, Hilary W, Onyike, Chiadi, Tartaglia, Carmela, Domoto-Reilly, Kimiko, Roberson, Erik D, Mendez, Mario F, Litvan, Irene, Appleby, Brian S, Grant, Ian, Kaufer, Daniel, Boxer, Adam L, Rosen, Howard J, Boeve, Brad F, Wszolek, Zbigniew K
Publikováno v:
Neurology, vol 99, iss 11
Familial frontotemporal lobar degeneration (f-FTLD) is a phenotypically heterogeneous spectrum of neurodegenerative disorders most often caused by variants within chromosome 9 open reading frame 72 (C9orf72), microtubule-associated protein tau (MAPT)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::072cc1d298afc8bfdcbde772d2a41851
https://escholarship.org/uc/item/2vq438vx
https://escholarship.org/uc/item/2vq438vx
Autor:
Bouzigues, Arabella, Russell, Lucy L, Tiraboschi, Pietro, Lladó, Albert, Antonell, Anna, Olives, Jaume, Balasa, Mircea, Bargalló, Nuria, Borrego-Ecija, Sergi, Verdelho, Ana, Maruta, Carolina, Ferreira, Catarina B, Miltenberger, Gabriel, Masellis, Mario, do Couto, Frederico Simões, Gabilondo, Alazne, Gorostidi, Ana, Villanua, Jorge, Cañada, Marta, Tainta, Mikel, Zulaica, Miren, Barandiaran, Myriam, Alves, Patricia, Bender, Benjamin, Tartaglia, Maria Carmela, Wilke, Carlo, Graf, Lisa, Vogels, Annick, Vandenbulcke, Mathieu, Van Damme, Philip, Bruffaerts, Rose, Poesen, Koen, Rosa-Neto, Pedro, Gauthier, Serge, Camuzat, Agnès, Finger, Elizabeth, Brice, Alexis, Bertrand, Anne, Funkiewiez, Aurélie, Rinaldi, Daisy, Saracino, Dario, Colliot, Olivier, Sayah, Sabrina, Prix, Catharina, Wlasich, Elisabeth, Wagemann, Olivia, van Swieten, John C, Loosli, Sandra, Schönecker, Sonja, Hoegen, Tobias, Lombardi, Jolina, Anderl-Straub, Sarah, Rollin, Adeline, Kuchcinski, Gregory, Bertoux, Maxime, Lebouvier, Thibaud, Deramecourt, Vincent, Seelaar, Harro, Santiago, Beatriz, Duro, Diana, Leitão, Maria João, Almeida, Maria Rosario, Tábuas-Pereira, Miguel, Afonso, Sónia, Engel, Annerose, Polyakova, Maryna, Jiskoot, Lize, Sorbi, Sandro, Butler, Chris R, Graff, Caroline, Peakman, Georgia, Gerhard, Alexander, Langheinrich, Tobias, Laforce, Robert, Sanchez-Valle, Raquel, de Mendonça, Alexandre, Moreno, Fermin, Synofzik, Matthis, Vandenberghe, Rik, Ducharme, Simon, Le Ber, Isabelle, Bocchetta, Martina, Levin, Johannes, Danek, Adrian, Otto, Markus, Pasquier, Florence, Santana, Isabel, Rohrer, Jonathan D, Genetic FTD Initiative, GENFI, Esteve, Aitana Sogorb, Nelson, Annabel, Greaves, Caroline V, Heller, Carolin, Cash, David, Thomas, David L, Todd, Emily, Benotmane, Hanya, Zetterberg, Henrik, Swift, Imogen J, Nicholas, Jennifer, Samra, Kiran, Convery, Rhian S, Shafei, Rachelle, Timberlake, Carolyn, Cope, Thomas, Rittman, Timothy, Benussi, Alberto, Premi, Enrico, Gasparotti, Roberto, Archetti, Silvana, Gazzina, Stefano, Cantoni, Valentina, Arighi, Andrea, Fenoglio, Chiara, Scarpini, Elio, Fumagalli, Giorgio, Borracci, Vittoria, Rossi, Giacomina, Giaccone, Giorgio, Rowe, James B, Caroppo, Paola, Prioni, Sara, Redaelli, Veronica, Tang-Wai, David, Rogaeva, Ekaterina, Castelo-Branco, Miguel, Keren, Ron, Black, Sandra, Mitchell, Sara, Borroni, Barbara, Shoesmith, Christen, Bartha, Robart, Rademakers, Rosa, Poos, Jackie, Papma, Janne M, Giannini, Lucia, Minkelen, Rick, Pijnenburg, Yolande, Nacmias, Benedetta, Ferrari, Camilla, Galimberti, Daniela, Polito, Cristina, Lombardi, Gemma, Bessi, Valentina, Veldsman, Michele, Andersson, Christin, Thonberg, Hakan, Öijerstedt, Linn, Jelic, Vesna, Thompson, Paul
Publikováno v:
Neuroscience Institute Publications
Journal of neurology
Journal of neurology 269(8), 4322-4332 (2022). doi:10.1007/s00415-022-11068-0
Journal of Neurology, 269(8), 4322-4332. D. Steinkopff-Verlag
Journal of neurology
Journal of neurology 269(8), 4322-4332 (2022). doi:10.1007/s00415-022-11068-0
Journal of Neurology, 269(8), 4322-4332. D. Steinkopff-Verlag
Funder: Alzheimer’s Research UK; doi: http://dx.doi.org/10.13039/501100002283
Funder: UCLH Biomedical Research Centre; doi: http://dx.doi.org/10.13039/501100012317
Funder: Medical Research Council; doi: http://dx.doi.org/10.13039/50110000
Funder: UCLH Biomedical Research Centre; doi: http://dx.doi.org/10.13039/501100012317
Funder: Medical Research Council; doi: http://dx.doi.org/10.13039/50110000
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::253504769e6b979d2e94f9f8340758e3
https://www.repository.cam.ac.uk/handle/1810/339275
https://www.repository.cam.ac.uk/handle/1810/339275
Autor:
Suzanne S. M. Miedema, Merel O. Mol, Frank T. W. Koopmans, David C. Hondius, Pim van Nierop, Kevin Menden, Christina F. de Veij Mestdagh, Jeroen van Rooij, Andrea B. Ganz, Iryna Paliukhovich, Shamiram Melhem, Ka Wan Li, Henne Holstege, Patrizia Rizzu, Ronald E. van Kesteren, John C. van Swieten, Peter Heutink, August B. Smit
Publikováno v:
Acta Neuropathologica Communications, 10:100, 1-20. BioMed Central
Acta Neuropathologica Communications 10, 100 (2022). doi:10.1186/s40478-022-01387-8
Acta neuropathologica communications, 10(1):100. BioMed Central
Miedema, S S M, Mol, M O, Koopmans, F T W, Hondius, D C, van Nierop, P, Menden, K, de Veij Mestdagh, C F, van Rooij, J, Ganz, A B, Paliukhovich, I, Melhem, S, Li, K W, Holstege, H, Rizzu, P, van Kesteren, R E, van Swieten, J C, Heutink, P & Smit, A B 2022, ' Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia ', Acta neuropathologica communications, vol. 10, no. 1, 100 . https://doi.org/10.1186/s40478-022-01387-8
Miedema, S S M, Mol, M O, Koopmans, F T W, Hondius, D C, van Nierop, P, Menden, K, de Veij Mestdagh, C F, van Rooij, J, Ganz, A B, Paliukhovich, I, Melhem, S, Li, K W, Holstege, H, Rizzu, P, van Kesteren, R E, van Swieten, J C, Heutink, P & Smit, A B 2022, ' Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia ', Acta Neuropathologica Communications, vol. 10, 100, pp. 1-20 . https://doi.org/10.1186/s40478-022-01387-8
Acta neuropathologica communications, 10(1):100. BioMed Central Ltd.
Acta Neuropathologica Communications 10, 100 (2022). doi:10.1186/s40478-022-01387-8
Acta neuropathologica communications, 10(1):100. BioMed Central
Miedema, S S M, Mol, M O, Koopmans, F T W, Hondius, D C, van Nierop, P, Menden, K, de Veij Mestdagh, C F, van Rooij, J, Ganz, A B, Paliukhovich, I, Melhem, S, Li, K W, Holstege, H, Rizzu, P, van Kesteren, R E, van Swieten, J C, Heutink, P & Smit, A B 2022, ' Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia ', Acta neuropathologica communications, vol. 10, no. 1, 100 . https://doi.org/10.1186/s40478-022-01387-8
Miedema, S S M, Mol, M O, Koopmans, F T W, Hondius, D C, van Nierop, P, Menden, K, de Veij Mestdagh, C F, van Rooij, J, Ganz, A B, Paliukhovich, I, Melhem, S, Li, K W, Holstege, H, Rizzu, P, van Kesteren, R E, van Swieten, J C, Heutink, P & Smit, A B 2022, ' Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia ', Acta Neuropathologica Communications, vol. 10, 100, pp. 1-20 . https://doi.org/10.1186/s40478-022-01387-8
Acta neuropathologica communications, 10(1):100. BioMed Central Ltd.
Frontotemporal dementia is characterized by progressive atrophy of frontal and/or temporal cortices at an early age of onset. The disorder shows considerable clinical, pathological, and genetic heterogeneity. Here we investigated the proteomic signat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16ed3f5c28d1f7163a6a79c1cdeb0f90
https://pure.eur.nl/en/publications/0bf4ae4a-7b76-48e9-a5b6-f7b814f744c3
https://pure.eur.nl/en/publications/0bf4ae4a-7b76-48e9-a5b6-f7b814f744c3
Autor:
Nelson, Annabel, Russell, Lucy L., Moreno, Fermin, Minkelen, Rick, Mitchell, Sara, Moore, Katrina, Nacmias, Benedetta, Öijerstedt, Linn, Olives, Jaume, Ourselin, Sebastien, Padovani, Alessandro, Panman, Jessica, Sanchez-Valle, Raquel, Papma, Janne M., Pijnenburg, Yolande, Polito, Cristina, Premi, Enrico, Prioni, Sara, Prix, Catharina, Rademakers, Rosa, Redaelli, Veronica, Rinaldi, Daisy, Rittman, Tim, Laforce, Robert, Rogaeva, Ekaterina, Rollin, Adeline, Rosa-Neto, Pedro, Rossi, Giacomina, Rossor, Martin, Santiago, Beatriz, Saracino, Dario, Sayah, Sabrina, Scarpini, Elio, Schönecker, Sonja, Graff, Caroline, Seelaar, Harro, Semler, Elisa, Shafei, Rachelle, Shoesmith, Christen, Swift, Imogen, Tábuas-Pereira, Miguel, Tainta, Mikel, Taipa, Ricardo, Tang-Wai, David, Thomas, David L., Masellis, Mario, Thompson, Paul, Thonberg, Hakan, Timberlake, Carolyn, Tiraboschi, Pietro, Todd, Emily, Van Damme, Philip, Vandenbulcke, Mathieu, Veldsman, Michele, Verdelho, Ana, Villanua, Jorge, Tartaglia, Maria Carmela, Warren, Jason, Wilke, Carlo, Wlasich, Elisabeth, Zetterberg, Henrik, Zulaica, Miren, Rowe, James B., Borroni, Barbara, Finger, Elizabeth, Synofzik, Matthis, Peakman, Georgia, Galimberti, Daniela, Vandenberghe, Rik, Mendonça, Alexandre, Butler, Chris R., Gerhard, Alexander, Ducharme, Simon, Le Ber, Isabelle, Santana, Isabel, Pasquier, Florence, Levin, Johannes, Convery, Rhian S., Otto, Markus, Sorbi, Sandro, Rohrer, Jonathan D., Afonso, Sónia, Almeida, Maria Rosario, Anderl-Straub, Sarah, Andersson, Christin, Antonell, Anna, Archetti, Silvana, Arighi, Andrea, Bouzigues, Arabella, Balasa, Mircea, Barandiaran, Myriam, Bargalló, Nuria, Bartha, Robart, Bender, Benjamin, Benussi, Alberto, Bertoux, Maxime, Bertrand, Anne, Bessi, Valentina, Black, Sandra, Greaves, Caroline V., Bocchetta, Martina, Borrego-Ecija, Sergi, Bras, Jose, Brice, Alexis, Bruffaerts, Rose, Camuzat, Agnès, Cañada, Marta, Cantoni, Valentina, Caroppo, Paola, Cash, David, Castelo-Branco, Miguel, Colliot, Olivier, Cope, Thomas, Deramecourt, Vincent, Arriba, María, Di Fede, Giuseppe, Díez, Alina, Duro, Diana, Fenoglio, Chiara, Ferrari, Camilla, Cash, David M., Ferreira, Catarina B., Fox, Nick, Freedman, Morris, Fumagalli, Giorgio, Funkiewiez, Aurélie, Gabilondo, Alazne, Gasparotti, Roberto, Gauthier, Serge, Gazzina, Stefano, Giaccone, Giorgio, Swieten, John C., Gorostidi, Ana, Greaves, Caroline, Guerreiro, Rita, Heller, Carolin, Hoegen, Tobias, Indakoetxea, Begoña, Jelic, Vesna, Karnath, Hans Otto, Keren, Ron, Kuchcinski, Gregory, Jiskoot, Lize, Langheinrich, Tobias, Lebouvier, Thibaud, Leitão, Maria João, Lladó, Albert, Lombardi, Gemma, Loosli, Sandra, Maruta, Carolina, Mead, Simon, Meeter, Lieke, Miltenberger, Gabriel
Publikováno v:
Annals of Clinical and Translational Neurology, 9(5), 644-658. John Wiley & Sons Inc.
Genetic FTD Initiative (GENFI) 2022, ' The CBI-R detects early behavioural impairment in genetic frontotemporal dementia ', Annals of Clinical and Translational Neurology, vol. 9, no. 5, pp. 644-658 . https://doi.org/10.1002/acn3.51544
Annals of Clinical and Translational Neurology 9(5), 644-658 (2022). doi:10.1002/acn3.51544
Neuroscience Institute Publications
Annals of Clinical and Translational Neurology, 9(5), 644-658. John Wiley and Sons Ltd
Genetic FTD Initiative (GENFI) 2022, ' The CBI-R detects early behavioural impairment in genetic frontotemporal dementia ', Annals of Clinical and Translational Neurology, vol. 9, no. 5, pp. 644-658 . https://doi.org/10.1002/acn3.51544
Annals of Clinical and Translational Neurology 9(5), 644-658 (2022). doi:10.1002/acn3.51544
Neuroscience Institute Publications
Annals of Clinical and Translational Neurology, 9(5), 644-658. John Wiley and Sons Ltd
Funder: UK Dementia Research Institute
Funder: NIHR UCL/H Biomedical Research Centre
Funder: The Wolfson Foundation
Funder: Brain Research UK; Id: http://dx.doi.org/10.13039/100013790
Funder: Alzheimer’s Research UK; Id: http://
Funder: NIHR UCL/H Biomedical Research Centre
Funder: The Wolfson Foundation
Funder: Brain Research UK; Id: http://dx.doi.org/10.13039/100013790
Funder: Alzheimer’s Research UK; Id: http://
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86be0d40188c38b37122db009034d261
https://pure.eur.nl/en/publications/ef3221c8-d0ab-4e8c-a674-961b339da3bc
https://pure.eur.nl/en/publications/ef3221c8-d0ab-4e8c-a674-961b339da3bc
Autor:
Johannes Levin, James B. Rowe, Raquel Sánchez-Valle, Fabrizio Tagliavini, Markus Otto, Jonathan D. Rohrer, Barbara Borroni, Robert Laforce, Adrian Danek, Isabel Santana, Daniela Galimberti, Caroline Graff, Christen Shoesmith, Giovanni B. Frisoni, Maria Carmela Tartaglia, Rik Vandenberghe, Tamara P. Tavares, Mario Masellis, Alexander Gerhard, Simon Ducharme, Roberta Ghidoni, Fermin Moreno, Sandro Sorbi, Elizabeth Finger, John C. van Swieten, Kristy Coleman, Matthis Synofzik, Derek G.V. Mitchell, Christopher C Butler, Alexandre de Mendonça, Brenda L. Coleman
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry 91(9), 975-984 (2020). doi:10.1136/jnnp-2020-322987
Journal of Neurology Neurosurgery and Psychiatry, 91(9), 975-984. BMJ Publishing Group
Journal of Neurology Neurosurgery and Psychiatry, 91(9), 975-984. BMJ Publishing Group
Funder: UK Medical Research Council
Funder: The Bluefield Project
Funder: NIHR Cambridge Biomedical Research Centre
Funder: Weston Brain Institute
Funder: Swedish Brain Foundation
Funder: StratNeuro, Swedish Demensfonden
Funder: The Bluefield Project
Funder: NIHR Cambridge Biomedical Research Centre
Funder: Weston Brain Institute
Funder: Swedish Brain Foundation
Funder: StratNeuro, Swedish Demensfonden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efcf5485858da8cc36f7cb18c5f06772
https://doi.org/10.1136/jnnp-2020-322987
https://doi.org/10.1136/jnnp-2020-322987
Autor:
Yolande A.L. Pijnenburg, Alessandro Padovani, Lieke H.H. Meeter, Rita Guerreiro, Mathieu Vandenbulcke, Rose Bruffaerts, Sonja Schönecker, Sofia Bergström, Florence Pasquier, Mikel Tainta, Beatriz Santiago, Roberto Gasparotti, Maria Rosário Almeida, Núria Bargalló, Abbe Ullgren, Martina Bocchetta, James B. Rowe, Pietro Tiraboschi, Robart Bartha, Rachelle Shafei, Benjamin Bender, Anna Månberg, Enrico Premi, Sergi Borrego-Écija, Sandro Sorbi, Christopher C Butler, Rick van Minkelen, Alberto Benussi, Marta Cañada, Carlo Wilke, Christin Andersson, Caroline Graff, Isabel Santana, Elisa Semler, Valentina Bessi, Miren Zulaica, Benedetta Nacmias, Tobias Langheinrich, Christen Shoesmith, Philip Van Damme, Camilla Ferrari, Martin Rosser, Pedro Rosa-Neto, Alexandre de Mendonça, Jennifer M. Nicholas, Catharina Prix, Sebastien Ourselin, Michele Veldsman, Jessica L. Panman, Håkan Thonberg, Jennie Olofsson, Paul M. Thompson, Ana Gorostidi, Andrea Arighi, Raquel Sánchez-Valle, Anna Antonell, Vesna Jelic, Ana Verdelho, Sara Mitchell, Janne M. Papma, Alina Díez, Giuliano Binetti, Rhian S Convery, Silvana Archetti, Ekaterina Rogaeva, Michela Pievani, C. Ferreira, Hans-Otto Karnath, Veronica Redaelli, Giuseppe Di Fede, Giovanni B. Frisoni, Carolina Maruta, Giacomina Rossi, Jaume Olives, Simon Ducharme, Roberta Ghidoni, Alexander Gerhard, Ron Keren, Johannes Levin, Sandra V. Loosli, Jose Bras, Isabelle Le Ber, Emily Todd, Robert Laforce, Sónia Afonso, Matthis Synofzik, Alazne Gabilondo, Elizabeth Finger, Thomas E. Cope, Paola Caroppo, Jorge Villanua, Diana Duro, Georgia Peakman, Giorgio G. Fumagalli, Serge Gauthier, Mario Masellis, Markus Otto, Caroline V. Greaves, Carolyn Timberlake, Harro Seelaar, Ione O.C. Woollacott, Sara Prioni, Jason D. Warren, Cristina Polito, Miguel Tábuas-Pereira, David F. Tang-Wai, Carmela Tartaglia, Linn Öijerstedt, Luisa Benussi, Barbara Borroni, Ricardo Taipa, Albert Lladó, Mircea Balasa, Rosa Rademakers, Lize C. Jiskoot, Miguel Castelo-Branco, Julia Remnestål, Fabrizio Tagliavini, Giorgio Giaccone, Maria João Leitão, Henrik Zetterberg, Valentina Cantoni, Daniela Galimberti, Sarah Anderl-Straub, Simon Mead, Myriam Barandiaran, Adrian Danek, Timothy Rittman, Chiara Fenoglio, Katrina M. Moore, David M. Cash, Rik Vandenberghe, Peter Nilsson, Elisabeth Wlasich, John C. van Swieten, Morris Freedman, Sandra E. Black, Carolin Heller, Stefano Gazzina, Gabriel Miltenberger, Fermin Moreno, Nick C. Fox, David L. Thomas, Jonathan D. Rohrer, Begoña Indakoetxea, Tobias Hoegen, Gemma Lombardi, Elio Scarpini
Publikováno v:
MOLECULAR NEURODEGENERATION, 16(1):79. BioMed Central
Molecular Neurodegeneration
Molecular Neurodegeneration, Vol 16, Iss 1, Pp 1-14 (2021)
Molecular Neurodegeneration, 16(1):79. BioMed Central Ltd.
Molecular neurodegeneration 16(1), 79 (2021). doi:10.1186/s13024-021-00499-4
on behalf of the Genetic Frontotemporal Dementia Initiative (GENFI) 2021, ' A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers : a GENFI study ', MOLECULAR NEURODEGENERATION, vol. 16, no. 1, 79 . https://doi.org/10.1186/s13024-021-00499-4
Molecular Neurodegeneration
Molecular Neurodegeneration, Vol 16, Iss 1, Pp 1-14 (2021)
Molecular Neurodegeneration, 16(1):79. BioMed Central Ltd.
Molecular neurodegeneration 16(1), 79 (2021). doi:10.1186/s13024-021-00499-4
on behalf of the Genetic Frontotemporal Dementia Initiative (GENFI) 2021, ' A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers : a GENFI study ', MOLECULAR NEURODEGENERATION, vol. 16, no. 1, 79 . https://doi.org/10.1186/s13024-021-00499-4
Availability of data and materials: The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request. Supplementary Information: Additional file 1 of A panel of CSF proteins separates geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01cfb7cc7522f0efcc55d0021b444921
https://doi.org/10.1186/s13024-021-00499-4
https://doi.org/10.1186/s13024-021-00499-4
Autor:
Heller, Carolin, Foiani, Martha S, Shafei, Rachelle, Miltenberger, Gabriel, Maruta, Carolina, Verdelho, Ana, Afonso, Sónia, Taipa, Ricardo, Caroppo, Paola, Fede, Giuseppe Di, Giaccone, Giorgio, Prioni, Sara, Redaelli, Veronica, Van Swieten, John C, Rossi, Giacomina, Tiraboschi, Pietro, Duro, Diana, Almeida, Maria Rosario, Castelo-Branco, Miguel, Leitão, Maria João, Tabuas-Pereira, Miguel, Santiago, Beatriz, Gauthier, Serge, Rosa-Neto, Pedro, Moreno, Fermin, Veldsman, Michele, Flanagan, Toby, Prix, Catharina, Hoegen, Tobias, Wlasich, Elisabeth, Loosli, Sandra, Schonecker, Sonja, Semler, Elisa, Anderl-Straub, Sarah, Benussi, Luisa, Sanchez-Valle, Raquel, Binetti, Giuliano, Ghidoni, Roberta, Pievani, Michela, Lombardi, Gemma, Nacmias, Benedetta, Ferrari, Camilla, Bessi, Valentina, Borroni, Barbara, Laforce, Robert, Masellis, Mario, Tartaglia, Maria Carmela, Graff, Caroline, Galimberti, Daniela, Moore, Katrina, Rowe, James B, Finger, Elizabeth, Synofzik, Matthis, Vandenberghe, Rik, de Mendonca, Alexandre, Tagliavini, Fabrizio, Santana, Isabel, Ducharme, Simon, Butler, Christopher R, Gerhard, Alex, Convery, Rhian, Levin, Johannes, Danek, Adrian, Frisoni, Giovanni, Sorbi, Sandro, Otto, Markus, Heslegrave, Amanda J, Zetterberg, Henrik, Rohrer, Jonathan D, GENFI, Rossor, Martin N, Bocchetta, Martina, Warren, Jason D, Fox, Nick C, Guerreiro, Rita, Bras, Jose, Nicholas, Jennifer, Mead, Simon, Jiskoot, Lize, Meeter, Lieke, Panman, Jessica, Papma, Janne, Neason, Mollie, Minkelen, Rick van, Pijnenburg, Yolanda, Barandiaran, Myriam, Indakoetxea, Begoña, Gabilondo, Alazne, Tainta, Mikel, Arriba, Maria de, Gorostidi, Ana, Zulaica, Miren, Villanua, Jorge, Cash, David M, Diaz, Zigor, Borrego-Ecija, Sergi, Olives, Jaume, Lladó, Albert, Balasa, Mircea, Antonell, Anna, Bargallo, Nuria, Premi, Enrico, Cosseddu, Maura, Gazzina, Stefano, Thomas, David, Padovani, Alessandro, Gasparotti, Roberto, Archetti, Silvana, Black, Sandra, Mitchell, Sara, Rogaeva, Ekaterina, Freedman, Morris, Keren, Ron, Tang-Wai, David, Öijerstedt, Linn, Greaves, Caroline V, Andersson, Christin, Jelic, Vesna, Thonberg, Hakan, Arighi, Andrea, Fenoglio, Chiara, Scarpini, Elio, Fumagalli, Giorgio, Cope, Thomas, Timberlake, Carolyn, Rittman, Timothy, Woollacott, Ione Oc, Shoesmith, Christen, Bartha, Robart, Rademakers, Rosa, Wilke, Carlo, Karnarth, Hans-Otto, Bender, Benjamin, Bruffaerts, Rose, Vandamme, Philip, Vandenbulcke, Mathieu, Ferreira, Catarina B
Publikováno v:
Medical Biophysics Publications
Journal of Neurology, Neurosurgery and Psychiatry, 91(3):2019321954. BMJ Publishing Group
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Heller, C, Foiani, M S, Moore, K, Convery, R, Bocchetta, M, Neason, M, Cash, D M, Thomas, D, Greaves, C V, Woollacott, I O C, Shafei, R, van Swieten, J C, Moreno, F, Sanchez-Valle, R, Borroni, B, Laforce, R, Masellis, M, Tartaglia, M C, Graff, C, Galimberti, D, Rowe, J B, Finger, E, Synofzik, M, Vandenberghe, R, de Mendonca, A, Tagliavini, F, Santana, I, Ducharme, S, Butler, C R, Gerhard, A, Levin, J, Danek, A, Frisoni, G, Sorbi, S, Otto, M, Heslegrave, A J, Zetterberg, H, Rohrer, J D, Rossor, M N, Warren, J D, Fox, N C, Guerreiro, R, Bras, J, Nicholas, J, Mead, S, Jiskoot, L, Meeter, L, Panman, J, Papma, J, van Minkelen, R, Pijnenburg, Y, Barandiaran, M, Indakoetxea, B, Gabilondo, A, Tainta, M, de Arriba, M, Gorostidi, A, Zulaica, M, Villanua, J, Diaz, Z, Borrego-Ecija, S, Olives, J, Lladó, A, Balasa, M, Antonell, A, Bargallo, N, Premi, E, Cosseddu, M, Gazzina, S, Padovani, A, Gasparotti, R, Archetti, S, Black, S, Mitchell, S, Rogaeva, E, Freedman, M, Keren, R, Tang-Wai, D, Öijerstedt, L, Andersson, C, Jelic, V, Thonberg, H, Arighi, A, Fenoglio, C, Scarpini, E, Fumagalli, G, Cope, T, Timberlake, C, Rittman, T, Shoesmith, C, Bartha, R, Rademakers, R, Wilke, C, Karnarth, H O, Bender, B, Bruffaerts, R, Vandamme, P, Vandenbulcke, M, Ferreira, C B, Miltenberger, G, Maruta, C, Verdelho, A, Afonso, S, Taipa, R, Caroppo, P, Di Fede, G, Giaccone, G, Prioni, S, Redaelli, V, Rossi, G, Tiraboschi, P, Dura, D, Almeida, M R, Castelo-Branco, M, João Leitão, M, Tabuas-Pereira, M, Santiago, B, Gauthier, S, Rosa-Neto, P, Veldsman, M, Flanagan, T, Prix, C, Hoegen, T, Wlasich, E, Loosli, S, Schonecker, S, Semler, E, Anderl-Straub, S, Benussi, L, Binetti, G, Ghidoni, R, Pievani, M, Lombardi, G, Nacmias, B, Ferrari, C, Bessi, V & GENFI 2020, ' Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia ', Journal of Neurology, Neurosurgery and Psychiatry, vol. 91, no. 3, 2019321954 . https://doi.org/10.1136/jnnp-2019-321954
Journal of neurology, neurosurgery, and psychiatry 91(3), 263-270 (2020). doi:10.1136/jnnp-2019-321954
Journal of Neurology Neurosurgery and Psychiatry, 91(3), 263-270. BMJ Publishing Group
Journal of Neurology, Neurosurgery and Psychiatry, 91(3):2019321954. BMJ Publishing Group
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Heller, C, Foiani, M S, Moore, K, Convery, R, Bocchetta, M, Neason, M, Cash, D M, Thomas, D, Greaves, C V, Woollacott, I O C, Shafei, R, van Swieten, J C, Moreno, F, Sanchez-Valle, R, Borroni, B, Laforce, R, Masellis, M, Tartaglia, M C, Graff, C, Galimberti, D, Rowe, J B, Finger, E, Synofzik, M, Vandenberghe, R, de Mendonca, A, Tagliavini, F, Santana, I, Ducharme, S, Butler, C R, Gerhard, A, Levin, J, Danek, A, Frisoni, G, Sorbi, S, Otto, M, Heslegrave, A J, Zetterberg, H, Rohrer, J D, Rossor, M N, Warren, J D, Fox, N C, Guerreiro, R, Bras, J, Nicholas, J, Mead, S, Jiskoot, L, Meeter, L, Panman, J, Papma, J, van Minkelen, R, Pijnenburg, Y, Barandiaran, M, Indakoetxea, B, Gabilondo, A, Tainta, M, de Arriba, M, Gorostidi, A, Zulaica, M, Villanua, J, Diaz, Z, Borrego-Ecija, S, Olives, J, Lladó, A, Balasa, M, Antonell, A, Bargallo, N, Premi, E, Cosseddu, M, Gazzina, S, Padovani, A, Gasparotti, R, Archetti, S, Black, S, Mitchell, S, Rogaeva, E, Freedman, M, Keren, R, Tang-Wai, D, Öijerstedt, L, Andersson, C, Jelic, V, Thonberg, H, Arighi, A, Fenoglio, C, Scarpini, E, Fumagalli, G, Cope, T, Timberlake, C, Rittman, T, Shoesmith, C, Bartha, R, Rademakers, R, Wilke, C, Karnarth, H O, Bender, B, Bruffaerts, R, Vandamme, P, Vandenbulcke, M, Ferreira, C B, Miltenberger, G, Maruta, C, Verdelho, A, Afonso, S, Taipa, R, Caroppo, P, Di Fede, G, Giaccone, G, Prioni, S, Redaelli, V, Rossi, G, Tiraboschi, P, Dura, D, Almeida, M R, Castelo-Branco, M, João Leitão, M, Tabuas-Pereira, M, Santiago, B, Gauthier, S, Rosa-Neto, P, Veldsman, M, Flanagan, T, Prix, C, Hoegen, T, Wlasich, E, Loosli, S, Schonecker, S, Semler, E, Anderl-Straub, S, Benussi, L, Binetti, G, Ghidoni, R, Pievani, M, Lombardi, G, Nacmias, B, Ferrari, C, Bessi, V & GENFI 2020, ' Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia ', Journal of Neurology, Neurosurgery and Psychiatry, vol. 91, no. 3, 2019321954 . https://doi.org/10.1136/jnnp-2019-321954
Journal of neurology, neurosurgery, and psychiatry 91(3), 263-270 (2020). doi:10.1136/jnnp-2019-321954
Journal of Neurology Neurosurgery and Psychiatry, 91(3), 263-270. BMJ Publishing Group
© Author(s) (or their employer(s)). No commercial re-use. See rights and permissions. Published by BMJ.
Background: There are few validated fluid biomarkers in frontotemporal dementia (FTD). Glial fibrillary acidic protein (GFAP) is a measure o
Background: There are few validated fluid biomarkers in frontotemporal dementia (FTD). Glial fibrillary acidic protein (GFAP) is a measure o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e104fbfc148264015ec3e00c8d0e5f4d
https://doi.org/10.1136/jnnp-2019-321954
https://doi.org/10.1136/jnnp-2019-321954
Autor:
Rachelle Shafei, Benjamin Bender, Jackie M. Poos, Maria Carmela Tartaglia, Janne M. Papma, Lieke H.H. Meeter, Isabel Santana, Christen Shoesmith, Mikel Tainta, Simon Mead, Albert Lladó, Alazne Gabilondo, Emanuela Rotondo, Alexander Gerhard, Simon Ducharme, Myriam Barandiaran, Mario Masellis, Caroline V. Greaves, Jaume Olives, Rita Guerreiro, Andrea Arighi, Diana Duro NPsych, Sara Mitchell, Roberto Gasparotti, Mathieu Vandenbulcke, Tobias Langheinrich, Thomas E. Cope, Martina Bocchetta, Robart Bartha, Daid Tang-Wai, Jessica L. Panman, Maria Rosário Almeida, Christopher C Butler, Rose Bruffaerts, Núria Bargalló, Pietro Tiraboschi, Beatriz Santiago, Elisabeth Wlasich, Philip Vandamme, Giorgio Giaccone, Sergi Borrego-Écija, Sonja Schönecker, Robert Laforce, Paola Caroppo, Katrina M. Moore, Ione O.C. Woollacott, Maria de Arriba, Veronica Redaelli, Rick van Minkelen, Jorge Villanua, Sónia Afonso, Matthis Synofzik, Nick C. Fox, Jennifer M. Nicholas, David L. Thomas, James B. Rowe, Carlo Wilke, Miren Zulaica, Pedro Rosa-Neto, Jonathan D. Rohrer, Elizabeth Finger, Carolyn Timberlake, C. Ferreira, David M. Cash, Timothy Rittman, Alessandro Padovani, Barbara Borroni, Ricardo Taipa, John C. van Swieten, Sandra V. Loosli, Begoña Indakoetxea, Daniela Galimberti, Sandra E. Black, Ana Gorostidi, Vesna Jelic, Catharina Prix, Ron Keren, Y.A.L. Pijnenburg, Michele Veldsman, Rosa Rademakers, Adrian Danek, Zigor Diaz, Miguel Tábuas-Pereira, Johannes Levin, Raquel Sánchez-Valle, Jose Bras, Rhian S Convery, Silvana Archetti, Markus Otto, Miguel Castelo-Branco, Rik Vandenberghe, Anna Antonell, Fabrizio Tagliavini, Sarah Anderl-Straub, Giuseppe Di Fede, Martin N. Rossor, Carolina Maruta MPsych, Enrico Premi, Giorgio G. Fumagalli, Sara Prioni, Cristina Muscio, Maria João Leitão, Lucy L. Russell, Håkan Thonberg, Ana Verdelho, Gabriel Miltenberger, Ekaterina Rogaeva, Giacomina Rossi, Linn Öijerstedt, Christin Andersson, Caroline Graff, Serge Gauthier, Maura Cosseddu MPsych, Carolin Heller, Stefano Gazzina, Jason D. Warren, Chiara Fenoglio, Tobias Hoegen, Elio Scarpini, Morris Freedman, Fermin Moreno, Mircea Balasa, Lize C. Jiskoot, Alexandre de Mendonça, Paul Thompson, Elisa Semler, Hans-Otto Karnarth
Publikováno v:
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior
Cortex 133, 384-398 (2020). doi:10.1016/j.cortex.2020.08.023
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Genetic FTD Initiative (GENFI) 2020, ' Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort ', Cortex, vol. 133, pp. 384-398 . https://doi.org/10.1016/j.cortex.2020.08.023
Cortex, 133, 384-398. Masson SpA
Russell, L L, Greaves, C V, Bocchetta, M, Nicholas, J, Convery, R S, Moore, K, Cash, D M, van Swieten, J, Jiskoot, L, Moreno, F, Sanchez-Valle, R, Borroni, B, Laforce, R, Masellis, M, Tartaglia, M C, Graff, C, Rotondo, E, Galimberti, D, Rowe, J B, Finger, E, Synofzik, M, Vandenberghe, R, de Mendonça, A, Tagliavini, F, Santana, I, Ducharme, S, Butler, C, Gerhard, A, Levin, J, Danek, A, Otto, M, Warren, J D, Rohrer, J D, Rossor, M N, Fox, N C, Woollacott, I O C, Shafei, R, Heller, C, Guerreiro, R, Bras, J, Thomas, D L, Mead, S, Meeter, L, Panman, J, Papma, J, Poos, J, van Minkelen, R, Pijnenburg, Y, Barandiaran, M, Indakoetxea, B, Gabilondo, A, Tainta, M, de Arriba, M, Gorostidi, A, Zulaica, M, Villanua, J, Diaz, Z, Borrego-Ecija, S, Olives, J, Lladó, A, Balasa, M, Antonell, A, Bargallo, N, Premi, E, Cosseddu MPsych, M, Gazzina, S, Padovani, A, Gasparotti, R, Archetti, S, Black, S, Mitchell, S, Rogaeva, E, Freedman, M, Keren, R, Tang-Wai, D, Öijerstedt, L, Andersson, C, Jelic, V, Thonberg, H, Arighi, A, Fenoglio, C, Scarpini, E, Fumagalli, G, Cope, T, Timberlake, C, Rittman, T, Shoesmith, C, Bartha, R, Rademakers, R, Wilke, C, Karnarth, H-O, Bender, B, Bruffaerts, R, Vandamme, P, Vandenbulcke, M, Ferreira, C B, Miltenberger, G, Maruta MPsych, C, Verdelho, A, Afonso, S N, Taipa, R, Caroppo, P, di Fede, G, Giaccone, G, Muscio, C, Prioni, S, Redaelli, V, Rossi, G, Tiraboschi, P, Duro NPsych, D, Almeida, M R, Castelo-Branco, M, Leitão, M J, Tabuas-Pereira, M, Santiago, B, Gauthier, S, Rosa-Neto, P, Veldsman, M, Thompson, P, Langheinrich, T, Prix, C, Hoegen, T, Wlasich, E, Loosli, S, Schonecker, S, the Genetic FTD Initiative, GENFI, Semler, E & Anderl-Straub, S 2020, ' Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort ', Cortex, vol. 133, pp. 384-398 . https://doi.org/10.1016/j.cortex.2020.08.023
Medical Biophysics Publications
Cortex 133, 384-398 (2020). doi:10.1016/j.cortex.2020.08.023
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Genetic FTD Initiative (GENFI) 2020, ' Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort ', Cortex, vol. 133, pp. 384-398 . https://doi.org/10.1016/j.cortex.2020.08.023
Cortex, 133, 384-398. Masson SpA
Russell, L L, Greaves, C V, Bocchetta, M, Nicholas, J, Convery, R S, Moore, K, Cash, D M, van Swieten, J, Jiskoot, L, Moreno, F, Sanchez-Valle, R, Borroni, B, Laforce, R, Masellis, M, Tartaglia, M C, Graff, C, Rotondo, E, Galimberti, D, Rowe, J B, Finger, E, Synofzik, M, Vandenberghe, R, de Mendonça, A, Tagliavini, F, Santana, I, Ducharme, S, Butler, C, Gerhard, A, Levin, J, Danek, A, Otto, M, Warren, J D, Rohrer, J D, Rossor, M N, Fox, N C, Woollacott, I O C, Shafei, R, Heller, C, Guerreiro, R, Bras, J, Thomas, D L, Mead, S, Meeter, L, Panman, J, Papma, J, Poos, J, van Minkelen, R, Pijnenburg, Y, Barandiaran, M, Indakoetxea, B, Gabilondo, A, Tainta, M, de Arriba, M, Gorostidi, A, Zulaica, M, Villanua, J, Diaz, Z, Borrego-Ecija, S, Olives, J, Lladó, A, Balasa, M, Antonell, A, Bargallo, N, Premi, E, Cosseddu MPsych, M, Gazzina, S, Padovani, A, Gasparotti, R, Archetti, S, Black, S, Mitchell, S, Rogaeva, E, Freedman, M, Keren, R, Tang-Wai, D, Öijerstedt, L, Andersson, C, Jelic, V, Thonberg, H, Arighi, A, Fenoglio, C, Scarpini, E, Fumagalli, G, Cope, T, Timberlake, C, Rittman, T, Shoesmith, C, Bartha, R, Rademakers, R, Wilke, C, Karnarth, H-O, Bender, B, Bruffaerts, R, Vandamme, P, Vandenbulcke, M, Ferreira, C B, Miltenberger, G, Maruta MPsych, C, Verdelho, A, Afonso, S N, Taipa, R, Caroppo, P, di Fede, G, Giaccone, G, Muscio, C, Prioni, S, Redaelli, V, Rossi, G, Tiraboschi, P, Duro NPsych, D, Almeida, M R, Castelo-Branco, M, Leitão, M J, Tabuas-Pereira, M, Santiago, B, Gauthier, S, Rosa-Neto, P, Veldsman, M, Thompson, P, Langheinrich, T, Prix, C, Hoegen, T, Wlasich, E, Loosli, S, Schonecker, S, the Genetic FTD Initiative, GENFI, Semler, E & Anderl-Straub, S 2020, ' Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort ', Cortex, vol. 133, pp. 384-398 . https://doi.org/10.1016/j.cortex.2020.08.023
Medical Biophysics Publications
© 2020 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
A key symptom of frontotemporal dementia (FTD) is difficulty interacting socially with others
A key symptom of frontotemporal dementia (FTD) is difficulty interacting socially with others
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7f473ba7ad713c07f0bee456df92fa2
http://europepmc.org/articles/PMC7754789
http://europepmc.org/articles/PMC7754789