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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Frontotemporal Lobar Degeneration and SQSTM1[original query]
SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Neurology 2012 Oct 79 (15): 1556-62.
Rubino Elisa, Rainero Innocenzo, Chiò Adriano, Rogaeva Ekaterina, Galimberti Daniela, Fenoglio Pierpaola, Grinberg Yakov, Isaia Giancarlo, Calvo Andrea, Gentile Salvatore, Bruni Amalia Cecilia, St George-Hyslop Peter Henry, Scarpini Elio, Gallone Salvatore, Pinessi Lorenzo,
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.
Acta neuropathologica 2014 Sep 128 (3): 397-410.
van der Zee Julie, Van Langenhove Tim, Kovacs Gabor G, Dillen Lubina, Deschamps William, Engelborghs Sebastiaan, Mat?j Radoslav, Vandenbulcke Mathieu, Sieben Anne, Dermaut Bart, Smets Katrien, Van Damme Philip, Merlin Céline, Laureys Annelies, Van Den Broeck Marleen, Mattheijssens Maria, Peeters Karin, Benussi Luisa, Binetti Giuliano, Ghidoni Roberta, Borroni Barbara, Padovani Alessandro, Archetti Silvana, Pastor Pau, Razquin Cristina, Ortega-Cubero Sara, Hernández Isabel, Boada Mercè, Ruiz Agustín, de Mendonça Alexandre, Miltenberger-Miltényi Gabriel, do Couto Frederico Simões, Sorbi Sandro, Nacmias Benedetta, Bagnoli Silvia, Graff Caroline, Chiang Huei-Hsin, Thonberg Håkan, Perneczky Robert, Diehl-Schmid Janine, Alexopoulos Panagiotis, Frisoni Giovanni B, Bonvicini Christian, Synofzik Matthis, Maetzler Walter, vom Hagen Jennifer Müller, Schöls Ludger, Haack Tobias B, Strom Tim M, Prokisch Holger, Dols-Icardo Oriol, Clarimón Jordi, Lleó Alberto, Santana Isabel, Almeida Maria Rosário, Santiago Beatriz, Heneka Michael T, Jessen Frank, Ramirez Alfredo, Sanchez-Valle Raquel, Llado Albert, Gelpi Ellen, Sarafov Stayko, Tournev Ivailo, Jordanova Albena, Parobkova Eva, Fabrizi Gian Maria, Testi Silvia, Salmon Eric, Ströbel Thomas, Santens Patrick, Robberecht Wim, De Jonghe Peter, Martin Jean-Jacques, Cras Patrick, Vandenberghe Rik, De Deyn Peter Paul, Cruts Marc, Sleegers Kristel, Van Broeckhoven Christi
Clinicopathological description of two cases with SQSTM1 gene mutation associated with frontotemporal dementia.
Neuropathology : official journal of the Japanese Society of Neuropathology 2015 Aug .
Kovacs Gabor G, van der Zee Julie, Hort Jakub, Kristoferitsch Wolfgang, Leitha Thomas, Höftberger Romana, Ströbel Thomas, Van Broeckhoven Christine, Matej Radosl
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations.
Journal of Alzheimer's disease : JAD 2016 May .
Luis Elkin, Ortiz Alexandra, Eudave Luis, Ortega-Cubero Sara, Borroni Barbara, van der Zee Julie, Gazzina Stefano, Caroppo Paola, Rubino Elisa, D'Agata Federico, Le Ber Isabelle, Santana Isabel, Cunha Gil, Almeida Maria R, Boutoleau-Bretonnière Claire, Hannequin Didier, Wallon David, Rainero Innocenzo, Galimberti Daniela, Van Broeckhoven Christine, Pastor Maria A, Pastor P
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