145 related articles for article (PubMed ID: 20561037)
21. Hyperexcitability and epileptic seizures in a model of frontotemporal dementia.
García-Cabrero AM; Guerrero-López R; Giráldez BG; Llorens-Martín M; Avila J; Serratosa JM; Sánchez MP
Neurobiol Dis; 2013 Oct; 58():200-8. PubMed ID: 23774255
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene.
Olszewska DA; Fearon C; McGuigan C; McVeigh TP; Houlden H; Polke JM; Lawlor B; Coen R; Hutchinson M; Hutton M; Beausang A; Delon I; Brett F; Sevastou I; Seto-Salvia N; de Silva R; Lynch T
Neurobiol Aging; 2021 Oct; 106():343.e1-343.e8. PubMed ID: 34274155
[TBL] [Abstract][Full Text] [Related]
24. Frontotemporal dementia-associated N279K tau mutant disrupts subcellular vesicle trafficking and induces cellular stress in iPSC-derived neural stem cells.
Wren MC; Zhao J; Liu CC; Murray ME; Atagi Y; Davis MD; Fu Y; Okano HJ; Ogaki K; Strongosky AJ; Tacik P; Rademakers R; Ross OA; Dickson DW; Wszolek ZK; Kanekiyo T; Bu G
Mol Neurodegener; 2015 Sep; 10():46. PubMed ID: 26373282
[TBL] [Abstract][Full Text] [Related]
25. Refining frontotemporal dementia with parkinsonism linked to chromosome 17: introducing FTDP-17 (MAPT) and FTDP-17 (PGRN).
Boeve BF; Hutton M
Arch Neurol; 2008 Apr; 65(4):460-4. PubMed ID: 18413467
[TBL] [Abstract][Full Text] [Related]
26. Clinical aspects of familial forms of frontotemporal dementia associated with parkinsonism.
Fujioka S; Wszolek ZK
J Mol Neurosci; 2011 Nov; 45(3):359-65. PubMed ID: 21656039
[TBL] [Abstract][Full Text] [Related]
27. Frontotemporal dementia with parkinsonism linked to chromosome 17 with the MAPT R406W mutation presenting with a broad distribution of abundant senile plaques.
Ishida C; Kobayashi K; Kitamura T; Ujike H; Iwasa K; Yamada M
Neuropathology; 2015 Feb; 35(1):75-82. PubMed ID: 25377499
[TBL] [Abstract][Full Text] [Related]
28. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.
Zarranz JJ; Ferrer I; Lezcano E; Forcadas MI; Eizaguirre B; Atarés B; Puig B; Gómez-Esteban JC; Fernández-Maiztegui C; Rouco I; Pérez-Concha T; Fernández M; Rodríguez O; Rodríguez-Martínez AB; de Pancorbo MM; Pastor P; Pérez-Tur J
Neurology; 2005 May; 64(9):1578-85. PubMed ID: 15883319
[TBL] [Abstract][Full Text] [Related]
29. Generation of an isogenic, gene-corrected iPSC line from a symptomatic 57-year-old female patient with frontotemporal dementia caused by a P301L mutation in the microtubule associated protein tau (MAPT) gene.
Nimsanor N; Kitiyanant N; Poulsen U; Rasmussen MA; Clausen C; Mau-Holzmann UA; Nielsen JE; Nielsen TT; Hyttel P; Holst B; Schmid B
Stem Cell Res; 2016 Nov; 17(3):556-559. PubMed ID: 27789409
[TBL] [Abstract][Full Text] [Related]
30. Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family.
Lossos A; Reches A; Gal A; Newman JP; Soffer D; Gomori JM; Boher M; Ekstein D; Biran I; Meiner Z; Abramsky O; Rosenmann H
J Neurol; 2003 Jun; 250(6):733-40. PubMed ID: 12796837
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Hereditary frontotemporal dementia caused by Tau gene mutations.
van Swieten J; Spillantini MG
Brain Pathol; 2007 Jan; 17(1):63-73. PubMed ID: 17493040
[TBL] [Abstract][Full Text] [Related]
33. Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation.
Baba Y; Baker MC; Le Ber I; Brice A; Maeck L; Kohlhase J; Yasuda M; Stoppe G; Bugiani O; Sperfeld AD; Tsuboi Y; Uitti RJ; Farrer MJ; Ghetti B; Hutton ML; Wszolek ZK
J Neural Transm (Vienna); 2007 Jul; 114(7):947-50. PubMed ID: 17318302
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging.
Ghetti B; Oblak AL; Boeve BF; Johnson KA; Dickerson BC; Goedert M
Neuropathol Appl Neurobiol; 2015 Feb; 41(1):24-46. PubMed ID: 25556536
[TBL] [Abstract][Full Text] [Related]
36. Induced pluripotent stem cells (iPSCs) derived from a symptomatic carrier of a S305I mutation in the microtubule-associated protein tau (MAPT)-gene causing frontotemporal dementia.
Nimsanor N; Jørring I; Rasmussen MA; Clausen C; Mau-Holzmann UA; Kitiyanant N; Nielsen JE; Nielsen TT; Hyttel P; Holst B; Schmid B
Stem Cell Res; 2016 Nov; 17(3):564-567. PubMed ID: 27789411
[TBL] [Abstract][Full Text] [Related]
37. Novel P397S MAPT variant associated with late onset and slow progressive frontotemporal dementia.
Borrego-Écija S; Antonell A; Puig-Butillé JA; Pericot I; Prat-Bravo C; Abellan-Vidal MT; Mallada J; Olives J; Falgàs N; Oliva R; Lladó A; Sánchez-Valle R
Ann Clin Transl Neurol; 2019 Aug; 6(8):1559-1565. PubMed ID: 31402617
[TBL] [Abstract][Full Text] [Related]
38. Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.
Dumanchin C; Camuzat A; Campion D; Verpillat P; Hannequin D; Dubois B; Saugier-Veber P; Martin C; Penet C; Charbonnier F; Agid Y; Frebourg T; Brice A
Hum Mol Genet; 1998 Oct; 7(11):1825-9. PubMed ID: 9736786
[TBL] [Abstract][Full Text] [Related]
39. In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17.
Ghetti B; Spina S; Murrell JR; Huey ED; Pietrini P; Sweeney B; Wassermann EM; Keohane C; Farlow MR; Grafman J
Neurodegener Dis; 2008; 5(3-4):215-7. PubMed ID: 18322394
[TBL] [Abstract][Full Text] [Related]
40. Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation.
Larner AJ
J Neurol Sci; 2009 Dec; 287(1-2):253-6. PubMed ID: 19766248
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]