944 related articles for article (PubMed ID: 26476236)
1. TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts.
Le Ber I; De Septenville A; Millecamps S; Camuzat A; Caroppo P; Couratier P; Blanc F; Lacomblez L; Sellal F; Fleury MC; Meininger V; Cazeneuve C; Clot F; Flabeau O; LeGuern E; Brice A;
Neurobiol Aging; 2015 Nov; 36(11):3116.e5-3116.e8. PubMed ID: 26476236
[TBL] [Abstract][Full Text] [Related]
2. Association between TBK1 mutations and risk of amyotrophic lateral sclerosis/frontotemporal dementia spectrum: a meta-analysis.
Cui R; Tuo M; Li P; Zhou C
Neurol Sci; 2018 May; 39(5):811-820. PubMed ID: 29349657
[TBL] [Abstract][Full Text] [Related]
3. TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
van der Zee J; Gijselinck I; Van Mossevelde S; Perrone F; Dillen L; Heeman B; Bäumer V; Engelborghs S; De Bleecker J; Baets J; Gelpi E; Rojas-García R; Clarimón J; Lleó A; Diehl-Schmid J; Alexopoulos P; Perneczky R; Synofzik M; Just J; Schöls L; Graff C; Thonberg H; Borroni B; Padovani A; Jordanova A; Sarafov S; Tournev I; de Mendonça A; Miltenberger-Miltényi G; Simões do Couto F; Ramirez A; Jessen F; Heneka MT; Gómez-Tortosa E; Danek A; Cras P; Vandenberghe R; De Jonghe P; De Deyn PP; Sleegers K; Cruts M; Van Broeckhoven C; Goeman J; Nuytten D; Smets K; Robberecht W; Damme PV; Bleecker J; Santens P; Dermaut B; Versijpt J; Michotte A; Ivanoiu A; Deryck O; Bergmans B; Delbeck J; Bruyland M; Willems C; Salmon E; Pastor P; Ortega-Cubero S; Benussi L; Ghidoni R; Binetti G; Hernández I; Boada M; Ruiz A; Sorbi S; Nacmias B; Bagnoli S; Sorbi S; Sanchez-Valle R; Llado A; Santana I; Rosário Almeida M; Frisoni GB; Maetzler W; Matej R; Fraidakis MJ; Kovacs GG; Fabrizi GM; Testi S
Hum Mutat; 2017 Mar; 38(3):297-309. PubMed ID: 28008748
[TBL] [Abstract][Full Text] [Related]
4. Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.
Gijselinck I; Van Mossevelde S; van der Zee J; Sieben A; Philtjens S; Heeman B; Engelborghs S; Vandenbulcke M; De Baets G; Bäumer V; Cuijt I; Van den Broeck M; Peeters K; Mattheijssens M; Rousseau F; Vandenberghe R; De Jonghe P; Cras P; De Deyn PP; Martin JJ; Cruts M; Van Broeckhoven C;
Neurology; 2015 Dec; 85(24):2116-25. PubMed ID: 26581300
[TBL] [Abstract][Full Text] [Related]
5. Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.
Van Mossevelde S; van der Zee J; Gijselinck I; Engelborghs S; Sieben A; Van Langenhove T; De Bleecker J; Baets J; Vandenbulcke M; Van Laere K; Ceyssens S; Van den Broeck M; Peeters K; Mattheijssens M; Cras P; Vandenberghe R; De Jonghe P; Martin JJ; De Deyn PP; Cruts M; Van Broeckhoven C;
Brain; 2016 Feb; 139(Pt 2):452-67. PubMed ID: 26674655
[TBL] [Abstract][Full Text] [Related]
6. Association of Mutations in TBK1 With Sporadic and Familial Amyotrophic Lateral Sclerosis and Frontotemporal Dementia.
Freischmidt A; Müller K; Ludolph AC; Weishaupt JH; Andersen PM
JAMA Neurol; 2017 Jan; 74(1):110-113. PubMed ID: 27892983
[TBL] [Abstract][Full Text] [Related]
7. Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients.
Chaussenot A; Le Ber I; Ait-El-Mkadem S; Camuzat A; de Septenville A; Bannwarth S; Genin EC; Serre V; Augé G; ; Brice A; Pouget J; Paquis-Flucklinger V
Neurobiol Aging; 2014 Dec; 35(12):2884.e1-2884.e4. PubMed ID: 25155093
[TBL] [Abstract][Full Text] [Related]
8. TBK1 variants in Chinese patients with amyotrophic lateral sclerosis: Genetic analysis and clinical features.
Zhao B; Jiang Q; Lin J; Wei Q; Li C; Hou Y; Cao B; Zhang L; Ou R; Liu K; Yang T; Xiao Y; Shang H
Eur J Neurol; 2023 Oct; 30(10):3079-3089. PubMed ID: 37422901
[TBL] [Abstract][Full Text] [Related]
9. Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.
Pottier C; Bieniek KF; Finch N; van de Vorst M; Baker M; Perkersen R; Brown P; Ravenscroft T; van Blitterswijk M; Nicholson AM; DeTure M; Knopman DS; Josephs KA; Parisi JE; Petersen RC; Boylan KB; Boeve BF; Graff-Radford NR; Veltman JA; Gilissen C; Murray ME; Dickson DW; Rademakers R
Acta Neuropathol; 2015 Jul; 130(1):77-92. PubMed ID: 25943890
[TBL] [Abstract][Full Text] [Related]
10. Functional and structural consequences of TBK1 missense variants in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Gurfinkel Y; Polain N; Sonar K; Nice P; Mancera RL; Rea SL
Neurobiol Dis; 2022 Nov; 174():105859. PubMed ID: 36113750
[TBL] [Abstract][Full Text] [Related]
11. Analysis of known amyotrophic lateral sclerosis and frontotemporal dementia genes reveals a substantial genetic burden in patients manifesting both diseases not carrying the
Dols-Icardo O; García-Redondo A; Rojas-García R; Borrego-Hernández D; Illán-Gala I; Muñoz-Blanco JL; Rábano A; Cervera-Carles L; Juárez-Rufián A; Spataro N; De Luna N; Galán L; Cortes-Vicente E; Fortea J; Blesa R; Grau-Rivera O; Lleó A; Esteban-Pérez J; Gelpi E; Clarimón J
J Neurol Neurosurg Psychiatry; 2018 Feb; 89(2):162-168. PubMed ID: 28889094
[TBL] [Abstract][Full Text] [Related]
12. Novel TBK1 variant associated with Frontotemporal Dementia overlap syndrome.
Arshad F; Vengalil S; Nalini A; Polavarapu K; Shamim U; Jabeen S; Nagaraj C; Ramakrishnan S; Faruq M; Alladi S
Acta Neurol Scand; 2022 Apr; 145(4):399-406. PubMed ID: 34841512
[TBL] [Abstract][Full Text] [Related]
13. Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline.
Piaceri I; Bessi V; Matà S; Polito C; Tedde A; Berti V; Bagnoli S; Braccia A; Del Mastio M; Pignone AM; Pupi A; Sorbi S; Nacmias B
J Alzheimers Dis; 2018; 61(1):41-46. PubMed ID: 29103041
[TBL] [Abstract][Full Text] [Related]
14. TBK1 is associated with ALS and ALS-FTD in Sardinian patients.
Borghero G; Pugliatti M; Marrosu F; Marrosu MG; Murru MR; Floris G; Cannas A; Occhineri P; Cau TB; Loi D; Ticca A; Traccis S; Manera U; Canosa A; Moglia C; Calvo A; Barberis M; Brunetti M; Gibbs JR; Renton AE; Errichiello E; Zoledziewska M; Mulas A; Qian Y; Din J; Pliner HA; Traynor BJ; Chiò A;
Neurobiol Aging; 2016 Jul; 43():180.e1-5. PubMed ID: 27156075
[TBL] [Abstract][Full Text] [Related]
15. [A Pair of Siblings with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis and a Novel Thr462Lysfs Mutation in the TBK1 Gene].
Schönecker S; Brendel M; van der Zee J; van Broeckhoven C; Rominger A; Danek A; Levin J
Fortschr Neurol Psychiatr; 2016 Aug; 84(8):494-8. PubMed ID: 27570907
[TBL] [Abstract][Full Text] [Related]
16. FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees.
Brenner D; Müller K; Lattante S; Yilmaz R; Knehr A; Freischmidt A; Ludolph AC; Andersen PM; Weishaupt JH
Neurogenetics; 2022 Jan; 23(1):59-65. PubMed ID: 34518945
[TBL] [Abstract][Full Text] [Related]
17. Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort.
Verheijen J; van der Zee J; Gijselinck I; Van den Bossche T; Dillen L; Heeman B; Gómez-Tortosa E; Lladó A; Sanchez-Valle R; Graff C; Pastor P; Pastor MA; Benussi L; Ghidoni R; Binetti G; Clarimon J; de Mendonça A; Gelpi E; Tsolaki M; Diehl-Schmid J; Nacmias B; Almeida MR; Borroni B; Matej R; Ruiz A; Engelborghs S; Vandenberghe R; De Deyn PP; Cruts M; Van Broeckhoven C; Sleegers K; ;
Neurobiol Aging; 2018 Feb; 62():245.e1-245.e7. PubMed ID: 29146049
[TBL] [Abstract][Full Text] [Related]
18. Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes.
Wilke C; Baets J; De Bleecker JL; Deconinck T; Biskup S; Hayer SN; Züchner S; Schüle R; De Jonghe P; Synofzik M
Neurobiol Aging; 2018 Feb; 62():244.e9-244.e13. PubMed ID: 29137817
[TBL] [Abstract][Full Text] [Related]
19. Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients.
Millecamps S; De Septenville A; Teyssou E; Daniau M; Camuzat A; Albert M; LeGuern E; Galimberti D; ; Brice A; Marie Y; Le Ber I
Neurobiol Aging; 2014 Dec; 35(12):2882.e13-2882.e15. PubMed ID: 25158920
[TBL] [Abstract][Full Text] [Related]
20. SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis.
Le Ber I; Camuzat A; Guerreiro R; Bouya-Ahmed K; Bras J; Nicolas G; Gabelle A; Didic M; De Septenville A; Millecamps S; Lenglet T; Latouche M; Kabashi E; Campion D; Hannequin D; Hardy J; Brice A;
JAMA Neurol; 2013 Nov; 70(11):1403-10. PubMed ID: 24042580
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
