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 *

213 related articles for article (PubMed ID: 31870644)

  • 1. Two pathologically confirmed cases of novel mutations in the MAPT gene causing frontotemporal dementia.
    Shafei R; Woollacott IOC; Mummery CJ; Bocchetta M; Guerreiro R; Bras J; Warren JD; Lashley T; Jaunmuktane Z; Rohrer JD
    Neurobiol Aging; 2020 Mar; 87():141.e15-141.e20. PubMed ID: 31870644
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Temporal Variant Frontotemporal Dementia is Associated with Globular Glial Tauopathy.
    Clark CN; Lashley T; Mahoney CJ; Warren JD; Revesz T; Rohrer JD
    Cogn Behav Neurol; 2015 Jun; 28(2):92-7. PubMed ID: 26102999
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A heterozygous splicing variant IVS9-7A > T in intron 9 of the MAPT gene in a patient with right-temporal variant frontotemporal dementia with atypical 4 repeat tauopathy.
    Mori K; Shigenobu K; Beck G; Uozumi R; Satake Y; Suzuki M; Kondo S; Gotoh S; Yonenobu Y; Kawai M; Suzuki Y; Saito Y; Morii E; Hasegawa M; Mochizuki H; Murayama S; Ikeda M
    Acta Neuropathol Commun; 2023 Aug; 11(1):130. PubMed ID: 37563653
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies.
    Forrest SL; Kril JJ; Stevens CH; Kwok JB; Hallupp M; Kim WS; Huang Y; McGinley CV; Werka H; Kiernan MC; Götz J; Spillantini MG; Hodges JR; Ittner LM; Halliday GM
    Brain; 2018 Feb; 141(2):521-534. PubMed ID: 29253099
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterizing the Clinical Features and Atrophy Patterns of
    Young AL; Bocchetta M; Russell LL; Convery RS; Peakman G; Todd E; Cash DM; Greaves CV; van Swieten J; Jiskoot L; Seelaar H; Moreno F; Sanchez-Valle R; Borroni B; Laforce R; Masellis M; Tartaglia MC; Graff C; Galimberti D; Rowe JB; Finger E; Synofzik M; Vandenberghe R; de Mendonça A; Tagliavini F; Santana I; Ducharme S; Butler C; Gerhard A; Levin J; Danek A; Otto M; Sorbi S; Williams SCR; Alexander DC; Rohrer JD;
    Neurology; 2021 Aug; 97(9):e941-e952. PubMed ID: 34158384
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tau PET Imaging with [18F]PM-PBB3 in Frontotemporal Dementia with MAPT Mutation.
    Su Y; Fu J; Yu J; Zhao Q; Guan Y; Zuo C; Li M; Tan H; Cheng X
    J Alzheimers Dis; 2020; 76(1):149-157. PubMed ID: 32444551
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy.
    Tacik P; Sanchez-Contreras M; DeTure M; Murray ME; Rademakers R; Ross OA; Wszolek ZK; Parisi JE; Knopman DS; Petersen RC; Dickson DW
    Neuropathol Appl Neurobiol; 2017 Apr; 43(3):200-214. PubMed ID: 27859539
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images.
    Whitwell JL; Boeve BF; Weigand SD; Senjem ML; Gunter JL; Baker MC; DeJesus-Hernandez M; Knopman DS; Wszolek ZK; Petersen RC; Rademakers R; Jack CR; Josephs KA
    Eur J Neurol; 2015 May; 22(5):745-52. PubMed ID: 25683866
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Intrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: a case report and literature review.
    Lin HC; Lin CH; Chen PL; Cheng SJ; Chen PH
    BMC Neurol; 2017 Sep; 17(1):186. PubMed ID: 28923025
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frontotemporal Dementia-Parkinsonism Due to
    Bhattacharjee S; Kobylecki C
    Tremor Other Hyperkinet Mov (N Y); 2023; 13():35. PubMed ID: 37746582
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features.
    Ikeda A; Shimada H; Nishioka K; Takanashi M; Hayashida A; Li Y; Yoshino H; Funayama M; Ueno Y; Hatano T; Sahara N; Suhara T; Higuchi M; Hattori N
    Mov Disord; 2019 Apr; 34(4):568-574. PubMed ID: 30773680
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotype Heterogeneity and Genotype Correlation of MAPT Mutations in a Chinese PUMCH Cohort.
    Mao C; Dong L; Li J; Huang X; Lei D; Wang J; Chu S; Liu C; Peng B; Cui L; Gao J
    J Mol Neurosci; 2021 May; 71(5):1015-1022. PubMed ID: 33006106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Closing the tau loop: the missing tau mutation.
    McCarthy A; Lonergan R; Olszewska DA; O'Dowd S; Cummins G; Magennis B; Fallon EM; Pender N; Huey ED; Cosentino S; O'Rourke K; Kelly BD; O'Connell M; Delon I; Farrell M; Spillantini MG; Rowland LP; Fahn S; Craig P; Hutton M; Lynch T
    Brain; 2015 Oct; 138(Pt 10):3100-9. PubMed ID: 26297556
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frontotemporal dementia with the V337M
    Spina S; Schonhaut DR; Boeve BF; Seeley WW; Ossenkoppele R; O'Neil JP; Lazaris A; Rosen HJ; Boxer AL; Perry DC; Miller BL; Dickson DW; Parisi JE; Jagust WJ; Murray ME; Rabinovici GD
    Neurology; 2017 Feb; 88(8):758-766. PubMed ID: 28130473
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tau Protein and Frontotemporal Dementias.
    Goedert M; Spillantini MG; Falcon B; Zhang W; Newell KL; Hasegawa M; Scheres SHW; Ghetti B
    Adv Exp Med Biol; 2021; 1281():177-199. PubMed ID: 33433876
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and neuroimaging characterization of the first frontotemporal dementia family carrying the MAPT p.K298E mutation.
    Pozzi FE; Aprea V; Giovannelli G; Lattuada F; Crivellaro C; Bertola F; Castelnovo V; Canu E; Filippi M; Appollonio I; Ferrarese C; Agosta F; Tremolizzo L
    Neurogenetics; 2024 Jul; 25(3):215-223. PubMed ID: 38592608
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frontotemporal Dementia Caused by the P301L Mutation in the MAPT Gene: Clinicopathological Features of 13 Cases from the Same Geographical Origin in Barcelona, Spain.
    Borrego-Écija S; Morgado J; Palencia-Madrid L; Grau-Rivera O; Reñé R; Hernández I; Almenar C; Balasa M; Antonell A; Molinuevo JL; Lladó A; Martínez de Pancorbo M; Gelpi E; Sánchez-Valle R
    Dement Geriatr Cogn Disord; 2017; 44(3-4):213-221. PubMed ID: 28934750
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study.
    Valentino RR; Scotton WJ; Roemer SF; Lashley T; Heckman MG; Shoai M; Martinez-Carrasco A; Tamvaka N; Walton RL; Baker MC; Macpherson HL; Real R; Soto-Beasley AI; Mok K; Revesz T; Christopher EA; DeTure M; Seeley WW; Lee EB; Frosch MP; Molina-Porcel L; Gefen T; Redding-Ochoa J; Ghetti B; Robinson AC; Kobylecki C; Rowe JB; Beach TG; Teich AF; Keith JL; Bodi I; Halliday GM; Gearing M; Arzberger T; Morris CM; White CL; Mechawar N; Boluda S; MacKenzie IR; McLean C; Cykowski MD; Wang SJ; Graff C; Nagra RM; Kovacs GG; Giaccone G; Neumann M; Ang LC; Carvalho A; Morris HR; Rademakers R; Hardy JA; Dickson DW; Rohrer JD; Ross OA;
    Lancet Neurol; 2024 May; 23(5):487-499. PubMed ID: 38631765
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations.
    Snowden JS; Adams J; Harris J; Thompson JC; Rollinson S; Richardson A; Jones M; Neary D; Mann DM; Pickering-Brown S
    Amyotroph Lateral Scler Frontotemporal Degener; 2015; 16(7-8):497-505. PubMed ID: 26473392
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GRN and MAPT Mutations in 2 Frontotemporal Dementia Research Centers in Brazil.
    Takada LT; Bahia VS; Guimarães HC; Costa TV; Vale TC; Rodriguez RD; Porto FH; Machado JC; Beato RG; Cesar KG; Smid J; Nascimento CF; Grinberg LT; Brucki SM; Maximino JR; Camargos ST; Chadi G; Caramelli P; Nitrini R
    Alzheimer Dis Assoc Disord; 2016; 30(4):310-317. PubMed ID: 27082848
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.