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Items: 1 to 20 of 129

1.

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. doi: 10.1001/archneur.65.4.460. Review.

3.

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. doi: 10.1159/000113706. Epub 2008 Mar 6.

4.

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.

Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, Lindholm C, Snowden J, Adamson J, Sadovnick AD, Rollinson S, Cannon A, Dwosh E, Neary D, Melquist S, Richardson A, Dickson D, Berger Z, Eriksen J, Robinson T, Zehr C, Dickey CA, Crook R, McGowan E, Mann D, Boeve B, Feldman H, Hutton M.

Nature. 2006 Aug 24;442(7105):916-9. Epub 2006 Jul 16.

PMID:
16862116
5.

Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.

Cruts M, Kumar-Singh S, Van Broeckhoven C.

Curr Alzheimer Res. 2006 Dec;3(5):485-91. Review.

PMID:
17168647
6.

Mutations in progranulin explain atypical phenotypes with variants in MAPT.

Pickering-Brown SM, Baker M, Gass J, Boeve BF, Loy CT, Brooks WS, Mackenzie IR, Martins RN, Kwok JB, Halliday GM, Kril J, Schofield PR, Mann DM, Hutton M.

Brain. 2006 Nov;129(Pt 11):3124-6.

PMID:
17071927
7.

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.

Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, van Duijn C, Peeters K, Sciot R, Santens P, De Pooter T, Mattheijssens M, Van den Broeck M, Cuijt I, Vennekens K, De Deyn PP, Kumar-Singh S, Van Broeckhoven C.

Nature. 2006 Aug 24;442(7105):920-4. Epub 2006 Jul 16.

PMID:
16862115
8.

Frontotemporal dementia and parkinsonism linked to chromosome 17.

Wszołek ZK, Słowiński J, Golan M, Dickson DW.

Folia Neuropathol. 2005;43(4):258-70. Review.

9.

[Japanese contribution to the understanding of frontotemporal dementia and parkinsonism linked to chromosome 17(FTDP-17)].

Tsuboi Y, Wszolek ZK, Mizuno Y, Kobayashi T, Yasuda M, Yamada T.

No To Shinkei. 2003 Feb;55(2):107-19. Review. Japanese.

PMID:
12684990
10.
11.
12.

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).

Wszolek ZK, Tsuboi Y, Ghetti B, Pickering-Brown S, Baba Y, Cheshire WP.

Orphanet J Rare Dis. 2006 Aug 9;1:30. Review.

13.

Clinicopathologic correlation in PGRN mutations.

Davion S, Johnson N, Weintraub S, Mesulam MM, Engberg A, Mishra M, Baker M, Adamson J, Hutton M, Rademakers R, Bigio EH.

Neurology. 2007 Sep 11;69(11):1113-21. Epub 2007 May 23.

14.

Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.

Boeve BF, Baker M, Dickson DW, Parisi JE, Giannini C, Josephs KA, Hutton M, Pickering-Brown SM, Rademakers R, Tang-Wai D, Jack CR Jr, Kantarci K, Shiung MM, Golde T, Smith GE, Geda YE, Knopman DS, Petersen RC.

Brain. 2006 Nov;129(Pt 11):3103-14. Epub 2006 Oct 9.

PMID:
17030535
15.

Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).

Spillantini MG, Van Swieten JC, Goedert M.

Neurogenetics. 2000 Mar;2(4):193-205. Review.

PMID:
10983715
16.

Hereditary frontotemporal dementia caused by Tau gene mutations.

van Swieten J, Spillantini MG.

Brain Pathol. 2007 Jan;17(1):63-73. Review.

PMID:
17493040
17.

Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.

Shiarli AM, Jennings R, Shi J, Bailey K, Davidson Y, Tian J, Bigio EH, Ghetti B, Murrell JR, Delisle MB, Mirra S, Crain B, Zolo P, Arima K, Iseki E, Murayama S, Kretzschmar H, Neumann M, Lippa C, Halliday G, Mackenzie J, Khan N, Ravid R, Dickson D, Wszolek Z, Iwatsubo T, Pickering-Brown SM, Mann DM.

Neuropathol Appl Neurobiol. 2006 Aug;32(4):374-87.

PMID:
16866983
18.

Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17.

van Swieten JC, Rosso SM, van Herpen E, Kamphorst W, Ravid R, Heutink P.

Dement Geriatr Cogn Disord. 2004;17(4):261-4. Review.

PMID:
15178932
19.

Progranulin null mutations in both sporadic and familial frontotemporal dementia.

Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, Laquerrière A, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas-Antérion C, Michel BF, Golfier V, Didic M, Salachas F, Duyckaerts C, Cruts M, Verpillat P, Van Broeckhoven C, Brice A; French Research Network on FTD/FTD-MND..

Hum Mutat. 2007 Sep;28(9):846-55.

PMID:
17436289
20.

Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS.

Ogaki K, Li Y, Takanashi M, Ishikawa K, Kobayashi T, Nonaka T, Hasegawa M, Kishi M, Yoshino H, Funayama M, Tsukamoto T, Shioya K, Yokochi M, Imai H, Sasaki R, Kokubo Y, Kuzuhara S, Motoi Y, Tomiyama H, Hattori N.

Parkinsonism Relat Disord. 2013 Jan;19(1):15-20. doi: 10.1016/j.parkreldis.2012.06.019. Epub 2012 Jul 18.

PMID:
22818528

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