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.
6. Cerebral blood flow in presymptomatic MAPT and GRN mutation carriers: A longitudinal arterial spin labeling study. Dopper EG; Chalos V; Ghariq E; den Heijer T; Hafkemeijer A; Jiskoot LC; de Koning I; Seelaar H; van Minkelen R; van Osch MJ; Rombouts SA; van Swieten JC Neuroimage Clin; 2016; 12():460-5. PubMed ID: 27625986 [TBL] [Abstract][Full Text] [Related]
7. 18F-MK-6240 tau-PET in genetic frontotemporal dementia. Levy JP; Bezgin G; Savard M; Pascoal TA; Finger E; Laforce R; Sonnen JA; Soucy JP; Gauthier S; Rosa-Neto P; Ducharme S Brain; 2022 Jun; 145(5):1763-1772. PubMed ID: 34664612 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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. [A Pair of Siblings with a rare R5H-Mutation in Exon 1 of the MAPT-Gene]. Henz S; Ackl N; Knels C; Rominger A; Flatz W; Teipel S; Huppertz HJ; Roeber S; Neumann M; Danek A Fortschr Neurol Psychiatr; 2015 Jul; 83(7):397-401. PubMed ID: 26200045 [TBL] [Abstract][Full Text] [Related]
12. MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism? Anfossi M; Bernardi L; Gallo M; Geracitano S; Colao R; Puccio G; Curcio SA; Frangipane F; Mirabelli M; Tomaino C; Smirne N; Maletta R; Bruni AC Alzheimer Dis Assoc Disord; 2011; 25(1):96-9. PubMed ID: 21343707 [TBL] [Abstract][Full Text] [Related]
13. Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America. Gatto EM; Allegri RF; Da Prat G; Chrem Mendez P; Hanna DS; Dorschner MO; Surace EI; Zabetian CP; Mata IF Neurobiol Aging; 2017 May; 53():195.e11-195.e17. PubMed ID: 28268100 [TBL] [Abstract][Full Text] [Related]
14. Unusually long duration and delayed penetrance in a family with FTD and mutation in MAPT (V337M). Domoto-Reilly K; Davis MY; Keene CD; Bird TD Am J Med Genet B Neuropsychiatr Genet; 2017 Jan; 174(1):70-74. PubMed ID: 26990251 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]