These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

374 related articles for article (PubMed ID: 26581300)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.
    Janssens J; Philtjens S; Kleinberger G; Van Mossevelde S; van der Zee J; Cacace R; Engelborghs S; Sieben A; Banzhaf-Strathmann J; Dillen L; Merlin C; Cuijt I; Robberecht C; Schmid B; Santens P; Ivanoiu A; Vandenbulcke M; Vandenberghe R; Cras P; De Deyn PP; Martin JJ; Maudsley S; Haass C; Cruts M; Van Broeckhoven C;
    Acta Neuropathol Commun; 2015 Nov; 3():68. PubMed ID: 26555887
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.
    Nguyen HP; Van Mossevelde S; Dillen L; De Bleecker JL; Moisse M; Van Damme P; Van Broeckhoven C; van der Zee J;
    Neurobiol Aging; 2018 Jan; 61():255.e1-255.e7. PubMed ID: 28935222
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing.
    Le Ber I; Camuzat A; Guillot-Noel L; Hannequin D; Lacomblez L; Golfier V; Puel M; Martinaud O; Deramecourt V; Rivaud-Pechoux S; Millecamps S; Vercelletto M; Couratier P; Sellal F; Pasquier F; Salachas F; Thomas-Antérion C; Didic M; Pariente J; Seilhean D; Ruberg M; Wargon I; Blanc F; Camu W; Michel BF; Berger E; Sauvée M; Thauvin-Robinet C; Mondon K; Tournier-Lasserve E; Goizet C; Fleury M; Viennet G; Verpillat P; Meininger V; Duyckaerts C; Dubois B; Brice A
    J Alzheimers Dis; 2013; 34(2):485-99. PubMed ID: 23254636
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients.
    Perrone F; Nguyen HP; Van Mossevelde S; Moisse M; Sieben A; Santens P; De Bleecker J; Vandenbulcke M; Engelborghs S; Baets J; Cras P; Vandenberghe R; De Jonghe P; De Deyn PP; Martin JJ; Van Damme P; Van Broeckhoven C; van der Zee J;
    Neurobiol Aging; 2017 Mar; 51():177.e9-177.e16. PubMed ID: 28069311
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sex differences in the prevalence of genetic mutations in FTD and ALS: A meta-analysis.
    Curtis AF; Masellis M; Hsiung GR; Moineddin R; Zhang K; Au B; Millett G; Mackenzie I; Rogaeva E; Tierney MC
    Neurology; 2017 Oct; 89(15):1633-1642. PubMed ID: 28916533
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 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. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 19.