160 related articles for article (PubMed ID: 31276859)
1. Novel TBK1 LoF variant in a family with upper motor neuron predominant motor neuron disease.
Costa MR; Gromicho M; Pronto-Laborinho AC; Miltenberger Miltényi G; de Carvalho M
J Neurol Sci; 2019 Aug; 403():117-118. PubMed ID: 31276859
[No Abstract] [Full Text] [Related]
2. Clinicopathologic correlations in a family with a
Hirsch-Reinshagen V; Alfaify OA; Hsiung GR; Pottier C; Baker M; Perkerson RB; Rademakers R; Briemberg H; Foti DJ; Mackenzie IR
Amyotroph Lateral Scler Frontotemporal Degener; 2019 Nov; 20(7-8):568-575. PubMed ID: 31244341
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Familial primary lateral sclerosis or dementia associated with Arg573Gly
Gómez-Tortosa E; Van der Zee J; Ruggiero M; Gijselinck I; Esteban-Pérez J; García-Redondo A; Borrego-Hernández D; Navarro E; Sainz MJ; Pérez-Pérez J; Cruts M; Van Broeckhoven C; Guerrero-López R;
J Neurol Neurosurg Psychiatry; 2017 Nov; 88(11):996-997. PubMed ID: 28365590
[No Abstract] [Full Text] [Related]
5. Intrafamilial heterogeneity in hereditary motor neuron disease.
Appelbaum JS; Roos RP; Salazar-Grueso EF; Buchman A; Iannaccone S; Glantz R; Siddique T; Maselli R
Neurology; 1992 Aug; 42(8):1488-92. PubMed ID: 1641141
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese origin.
Williams KL; McCann EP; Fifita JA; Zhang K; Duncan EL; Leo PJ; Marshall M; Rowe DB; Nicholson GA; Blair IP
Neurobiol Aging; 2015 Dec; 36(12):3334.e1-3334.e5. PubMed ID: 26350399
[TBL] [Abstract][Full Text] [Related]
8. Familial clustering of primary lateral sclerosis and amyotrophic lateral sclerosis: Supplementary evidence for a continuum.
Corcia P; Lunetta C; Couratier P; Vourc'h P; Gromicho M; Desnuelle C; Soriani MH; Pinto S; de Carvalho M
Eur J Neurol; 2021 Aug; 28(8):2780-2783. PubMed ID: 34110677
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosis.
Tohnai G; Nakamura R; Sone J; Nakatochi M; Yokoi D; Katsuno M; Watanabe H; Watanabe H; Ito M; Li Y; Izumi Y; Morita M; Taniguchi A; Kano O; Oda M; Kuwabara S; Abe K; Aiba I; Okamoto K; Mizoguchi K; Hasegawa K; Aoki M; Hattori N; Onodera O; Naruse H; Mitsui J; Takahashi Y; Goto J; Ishiura H; Morishita S; Yoshimura J; Doi K; Tsuji S; Nakashima K; Kaji R; Atsuta N; Sobue G;
Neurobiol Aging; 2018 Apr; 64():158.e15-158.e19. PubMed ID: 29398122
[TBL] [Abstract][Full Text] [Related]
11.
Pozzi L; Valenza F; Mosca L; Dal Mas A; Domi T; Romano A; Tarlarini C; Falzone YM; Tremolizzo L; Sorarù G; Cerri F; Ferraro PM; Basaia S; Agosta F; Fazio R; Comola M; Comi G; Ferrari M; Quattrini A; Lunetta C; Penco S; Bonanomi D; Carrera P; Riva N
J Neurol Neurosurg Psychiatry; 2017 Oct; 88(10):869-875. PubMed ID: 28822984
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Novel VRK1 Mutations in a Patient with Childhood-onset Motor Neuron Disease.
Yamaura G; Higashiyama Y; Kusama K; Kunii M; Tanaka K; Koyano S; Nakashima M; Tsurusaki Y; Miyake N; Saitsu H; Iwahashi Y; Joki H; Matsumoto N; Doi H; Tanaka F
Intern Med; 2019 Sep; 58(18):2715-2719. PubMed ID: 31178479
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Adult onset Sandhoff disease: a rare mimicker of amyotrophic lateral sclerosis.
Khoueiry M; Malek E; Salameh JS
Amyotroph Lateral Scler Frontotemporal Degener; 2020 Feb; 21(1-2):144-146. PubMed ID: 31512525
[TBL] [Abstract][Full Text] [Related]
16. Amyotrophic lateral sclerosis and motor neuron syndromes in Asia.
Shahrizaila N; Sobue G; Kuwabara S; Kim SH; Birks C; Fan DS; Bae JS; Hu CJ; Gourie-Devi M; Noto Y; Shibuya K; Goh KJ; Kaji R; Tsai CP; Cui L; Talman P; Henderson RD; Vucic S; Kiernan MC
J Neurol Neurosurg Psychiatry; 2016 Aug; 87(8):821-30. PubMed ID: 27093948
[TBL] [Abstract][Full Text] [Related]
17. Genetic epidemiology of motor neuron disease-associated variants in the Scottish population.
Black HA; Leighton DJ; Cleary EM; Rose E; Stephenson L; Colville S; Ross D; Warner J; Porteous M; Gorrie GH; Swingler R; Goldstein D; Harms MB; Connick P; Pal S; Aitman TJ; Chandran S
Neurobiol Aging; 2017 Mar; 51():178.e11-178.e20. PubMed ID: 28089114
[TBL] [Abstract][Full Text] [Related]
18. Motor neuron disease: loss-of-function mutations in TBK1 can cause familial ALS.
Chase A
Nat Rev Neurol; 2015 May; 11(5):246. PubMed ID: 25848921
[No Abstract] [Full Text] [Related]
19. Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain.
Dols-Icardo O; Nebot I; Gorostidi A; Ortega-Cubero S; Hernández I; Rojas-García R; García-Redondo A; Povedano M; Lladó A; Álvarez V; Sánchez-Juan P; Pardo J; Jericó I; Vázquez-Costa J; Sevilla T; Cardona F; Indakoechea B; Moreno F; Fernández-Torrón R; Muñoz-Llahuna L; Moreno-Grau S; Rosende-Roca M; Vela Á; Muñoz-Blanco JL; Combarros O; Coto E; Alcolea D; Fortea J; Lleó A; Sánchez-Valle R; Esteban-Pérez J; Ruiz A; Pastor P; López De Munain A; Pérez-Tur J; Clarimón J;
Brain; 2015 Dec; 138(Pt 12):e400. PubMed ID: 26152333
[No Abstract] [Full Text] [Related]
20. Neuropathological characterization of a novel TANK binding kinase (TBK1) gene loss of function mutation associated with amyotrophic lateral sclerosis.
Weinreich M; Shepheard SR; Verber N; Wyles M; Heath PR; Highley JR; Kirby J; Shaw PJ
Neuropathol Appl Neurobiol; 2020 Apr; 46(3):279-291. PubMed ID: 31498468
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
