Differential early subcortical involvement in genetic FTD within the GENFI cohort

Archive ouverte

Bocchetta, Martina | Todd, Emily, G | Peakman, Georgia | Cash, David, M | Convery, Rhian, S | Russell, Lucy, L | Thomas, David, L | Eugenio Iglesias, Juan | van Swieten, John, C | Jiskoot, Lize, C | Seelaar, Harro | Borroni, Barbara | Galimberti, Daniela | Sanchez-Valle, Raquel | Laforce, Robert | Moreno, Fermin | Synofzik, Matthis | Graff, Caroline | Masellis, Mario | Carmela Tartaglia, Maria | Rowe, James, B | Vandenberghe, Rik | Finger, Elizabeth | Tagliavini, Fabrizio | de Mendonça, Alexandre | Santana, Isabel | Butler, Chris, R | Ducharme, Simon | Gerhard, Alexander | Danek, Adrian | Levin, Johannes | Otto, Markus | Sorbi, Sandro | Le Ber, Isabelle | Pasquier, Florence | Rohrer, Jonathan, D | Afonso, Sónia | Rosario Almeida, Maria | Anderl-Straub, Sarah | Andersson, Christin | Antonell, Anna | Archetti, Silvana | Arighi, Andrea | Balasa, Mircea | Barandiaran, Myriam | Bargalló, Nuria | Bartha, Robart | Bender, Benjamin | Benussi, Alberto | Bertoux, Maxime | Bertrand, Anne | Bessi, Valentina | Black, Sandra | Borrego-Ecija, Sergi | Bras, Jose | Brice, Alexis | Bruffaerts, Rose | Camuzat, Agnès | Cañada, Marta | Cantoni, Valentina | Caroppo, Paola | Castelo-Branco, Miguel | Colliot, Olivier | Cope, Thomas | Deramecourt, Vincent | de Arriba, María | Di Fede, Giuseppe | Díez, Alina | Duro, Diana | Fenoglio, Chiara | Ferrari, Camilla | Ferreira, Catarina, B | Fox, Nick | Freedman, Morris | Fumagalli, Giorgio | Funkiewiez, Aurélie | Gabilondo, Alazne | Gasparotti, Roberto | Gauthier, Serge | Gazzina, Stefano | Giaccone, Giorgio | Gorostidi, Ana | Greaves, Caroline | Guerreiro, Rita | Heller, Carolin | Hoegen, Tobias | Indakoetxea, Begoña | Jelic, Vesna | Karnath, Hans-Otto | Keren, Ron | Kuchcinski, Gregory | Langheinrich, Tobias | Lebouvier, Thibaud | João Leitão, Maria | Lladó, Albert | Lombardi, Gemma | Loosli, Sandra | Maruta, Carolina | Mead, Simon | Meeter, Lieke | Miltenberger, Gabriel | van Minkelen, Rick | Mitchell, Sara | Moore, Katrina | Nacmias, Benedetta | Nelson, Annabel | Nicholas, Jennifer | Öijerstedt, Linn | Olives, Jaume | Ourselin, Sebastien | Padovani, Alessandro | Panman, Jessica | Papma, Janne, M | Pijnenburg, Yolande | Polito, Cristina | Premi, Enrico | Prioni, Sara | Prix, Catharina | Rademakers, Rosa | Rinaldi, Daisy | Redaelli, Veronica | Rittman, Tim | Rogaeva, Ekaterina | Rollin, Adeline | Rosa-Neto, Pedro | Rossi, Giacomina | Rossor, Martin | Santiago, Beatriz | Saracino, Dario | Sayah, Sabrina | Scarpini, Elio | Schönecker, Sonja | Semler, Elisa | Shafei, Rachelle | Shoesmith, Christen | Swift, Imogen | Tábuas-Pereira, Miguel | Tainta, Mikel | Taipa, Ricardo | Tang-Wai, David | Thompson, Paul | Thonberg, Hakan | Timberlake, Carolyn | Tiraboschi, Pietro | van Damme, Philip | Vandenbulcke, Mathieu | Veldsman, Michele | Verdelho, Ana | Villanua, Jorge | Warren, Jason | Wilke, Carlo | Woollacott, Ione | Wlasich, Elisabeth | Zetterberg, Henrik | Zulaica, Miren

Edité par CCSD ; Elsevier -

International audience

Suggestions

Du même auteur

Examining empathy deficits across familial forms of frontotemporal dementia within the GENFI cohort

Archive ouverte | Foster, Phoebe, H | CCSD

International audience. BackgroundReduced empathy is a common symptom in frontotemporal dementia (FTD). Although empathy deficits have been extensively researched in sporadic cases, few studies have explored the dif...

The Revised Self-Monitoring Scale detects early impairment of social cognition in genetic frontotemporal dementia within the GENFI cohort

Archive ouverte | Franklin, Hannah, D | CCSD

International audience. Background: Although social cognitive dysfunction is a major feature of frontotemporal dementia (FTD), it has been poorly studied in familial forms. A key goal of studies is to detect early c...

Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort: comparison with sporadic primary progressive aphasia

Archive ouverte | Samra, Kiran | CCSD

International audience. Primary progressive aphasia is most commonly a sporadic disorder, but in some cases, it can be genetic. This study aimed to understand the clinical, cognitive and imaging phenotype of the gen...

Chargement des enrichissements...