311 related articles for article (PubMed ID: 32185393)
1. CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.
Dobson-Stone C; Hallupp M; Shahheydari H; Ragagnin AMG; Chatterton Z; Carew-Jones F; Shepherd CE; Stefen H; Paric E; Fath T; Thompson EM; Blumbergs P; Short CL; Field CD; Panegyres PK; Hecker J; Nicholson G; Shaw AD; Fullerton JM; Luty AA; Schofield PR; Brooks WS; Rajan N; Bennett MF; Bahlo M; Landers JE; Piguet O; Hodges JR; Halliday GM; Topp SD; Smith BN; Shaw CE; McCann E; Fifita JA; Williams KL; Atkin JD; Blair IP; Kwok JB
Brain; 2020 Mar; 143(3):783-799. PubMed ID: 32185393
[TBL] [Abstract][Full Text] [Related]
2. Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis.
Dobson-Stone C; Luty AA; Thompson EM; Blumbergs P; Brooks WS; Short CL; Field CD; Panegyres PK; Hecker J; Solski JA; Blair IP; Fullerton JM; Halliday GM; Schofield PR; Kwok JB
Acta Neuropathol; 2013 Apr; 125(4):523-33. PubMed ID: 23338750
[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. Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p.
Hsiung GY; DeJesus-Hernandez M; Feldman HH; Sengdy P; Bouchard-Kerr P; Dwosh E; Butler R; Leung B; Fok A; Rutherford NJ; Baker M; Rademakers R; Mackenzie IR
Brain; 2012 Mar; 135(Pt 3):709-22. PubMed ID: 22344582
[TBL] [Abstract][Full Text] [Related]
5. Rapid in vitro quantification of TDP-43 and FUS mislocalisation for screening of gene variants implicated in frontotemporal dementia and amyotrophic lateral sclerosis.
Oyston LJ; Ubiparipovic S; Fitzpatrick L; Hallupp M; Boccanfuso LM; Kwok JB; Dobson-Stone C
Sci Rep; 2021 Jul; 11(1):14881. PubMed ID: 34290285
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. CYLD variants identified in Alzheimer's disease and frontotemporal dementia patients.
Xiao X; Xu T; Liu H; Liu X; Liao X; Zhou Y; Zhou L; Wang X; Zhu Y; Yang Q; Hao X; Liu Y; Jiang H; Guo J; Wang J; Tang B; Li J; Shen L; Jiao B
Ann Clin Transl Neurol; 2022 Oct; 9(10):1596-1601. PubMed ID: 36000313
[TBL] [Abstract][Full Text] [Related]
8. Is amyotrophic lateral sclerosis/frontotemporal dementia an autophagy disease?
Deng Z; Sheehan P; Chen S; Yue Z
Mol Neurodegener; 2017 Dec; 12(1):90. PubMed ID: 29282133
[TBL] [Abstract][Full Text] [Related]
9. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement.
Bannwarth S; Ait-El-Mkadem S; Chaussenot A; Genin EC; Lacas-Gervais S; Fragaki K; Berg-Alonso L; Kageyama Y; Serre V; Moore DG; Verschueren A; Rouzier C; Le Ber I; Augé G; Cochaud C; Lespinasse F; N'Guyen K; de Septenville A; Brice A; Yu-Wai-Man P; Sesaki H; Pouget J; Paquis-Flucklinger V
Brain; 2014 Aug; 137(Pt 8):2329-45. PubMed ID: 24934289
[TBL] [Abstract][Full Text] [Related]
10. Lysosome dysfunction as a cause of neurodegenerative diseases: Lessons from frontotemporal dementia and amyotrophic lateral sclerosis.
Root J; Merino P; Nuckols A; Johnson M; Kukar T
Neurobiol Dis; 2021 Jul; 154():105360. PubMed ID: 33812000
[TBL] [Abstract][Full Text] [Related]
11. Genetic and clinical landscape of Chinese frontotemporal dementia: dominance of TBK1 and OPTN mutations.
Nan H; Kim YJ; Chu M; Li D; Li J; Jiang D; Wu Y; Ohtsuka T; Wu L
Alzheimers Res Ther; 2024 Jun; 16(1):127. PubMed ID: 38872230
[TBL] [Abstract][Full Text] [Related]
12. C9orf72 ALS-FTD: recent evidence for dysregulation of the autophagy-lysosome pathway at multiple levels.
Beckers J; Tharkeshwar AK; Van Damme P
Autophagy; 2021 Nov; 17(11):3306-3322. PubMed ID: 33632058
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Defective cyclophilin A induces TDP-43 proteinopathy: implications for amyotrophic lateral sclerosis and frontotemporal dementia.
Pasetto L; Grassano M; Pozzi S; Luotti S; Sammali E; Migazzi A; Basso M; Spagnolli G; Biasini E; Micotti E; Cerovic M; Carli M; Forloni G; De Marco G; Manera U; Moglia C; Mora G; Traynor BJ; Chiò A; Calvo A; Bonetto V
Brain; 2021 Dec; 144(12):3710-3726. PubMed ID: 34972208
[TBL] [Abstract][Full Text] [Related]
15. Novel TARDBP missense mutation caused familial amyotrophic lateral sclerosis with frontotemporal dementia and parkinsonism.
Chen S; Zhou RL; Zhang W; Che CH; Feng SY; Huang HP; Liu CY; Zou ZY
Neurobiol Aging; 2021 Nov; 107():168-173. PubMed ID: 34175147
[TBL] [Abstract][Full Text] [Related]
16. CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.
Williams KL; Topp S; Yang S; Smith B; Fifita JA; Warraich ST; Zhang KY; Farrawell N; Vance C; Hu X; Chesi A; Leblond CS; Lee A; Rayner SL; Sundaramoorthy V; Dobson-Stone C; Molloy MP; van Blitterswijk M; Dickson DW; Petersen RC; Graff-Radford NR; Boeve BF; Murray ME; Pottier C; Don E; Winnick C; McCann EP; Hogan A; Daoud H; Levert A; Dion PA; Mitsui J; Ishiura H; Takahashi Y; Goto J; Kost J; Gellera C; Gkazi AS; Miller J; Stockton J; Brooks WS; Boundy K; Polak M; Muñoz-Blanco JL; Esteban-Pérez J; Rábano A; Hardiman O; Morrison KE; Ticozzi N; Silani V; de Belleroche J; Glass JD; Kwok JB; Guillemin GJ; Chung RS; Tsuji S; Brown RH; García-Redondo A; Rademakers R; Landers JE; Gitler AD; Rouleau GA; Cole NJ; Yerbury JJ; Atkin JD; Shaw CE; Nicholson GA; Blair IP
Nat Commun; 2016 Apr; 7():11253. PubMed ID: 27080313
[TBL] [Abstract][Full Text] [Related]
17. Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis.
van der Zee J; Dillen L; Baradaran-Heravi Y; Gossye H; Koçoğlu C; Cuyt I; Dermaut B; Sieben A; Baets J; De Jonghe P; Vandenberghe R; De Deyn P; Cras P; Engelborghs S; Van Broeckhoven C;
Neurobiol Dis; 2021 Aug; 156():105421. PubMed ID: 34118419
[TBL] [Abstract][Full Text] [Related]
18. SQSTM1 variant in disorders of the frontotemporal dementia-amyotrophic lateral sclerosis spectrum: identification of a novel heterozygous variant and a review of the literature.
Li W; Gao H; Dong X; Zheng D
J Neurol; 2021 Apr; 268(4):1351-1357. PubMed ID: 33125541
[TBL] [Abstract][Full Text] [Related]
19. Delineating the relationship between amyotrophic lateral sclerosis and frontotemporal dementia: Sequence and structure-based predictions.
Kumar V; Islam A; Hassan MI; Ahmad F
Biochim Biophys Acta; 2016 Sep; 1862(9):1742-54. PubMed ID: 27318084
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
