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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
658 related items for PubMed ID: 9629852
1. Tau is a candidate gene for chromosome 17 frontotemporal dementia. Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM, Anderson L, Andreadis A, Wiederholt WC, Raskind M, Schellenberg GD. Ann Neurol; 1998 Jun; 43(6):815-25. PubMed ID: 9629852 [Abstract] [Full Text] [Related]
2. Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22. Baker M, Kwok JB, Kucera S, Crook R, Farrer M, Houlden H, Isaacs A, Lincoln S, Onstead L, Hardy J, Wittenberg L, Dodd P, Webb S, Hayward N, Tannenberg T, Andreadis A, Hallupp M, Schofield P, Dark F, Hutton M. Ann Neurol; 1997 Nov; 42(5):794-8. PubMed ID: 9392579 [Abstract] [Full Text] [Related]
3. Search for a mutation in the tau gene in a Swiss family with frontotemporal dementia. Savioz A, Kövari E, Anastasiu R, Rossier C, Saini K, Bouras C, Leuba G. Exp Neurol; 2000 Jan; 161(1):330-5. PubMed ID: 10683298 [Abstract] [Full Text] [Related]
4. Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval. Rademakers R, Cruts M, Dermaut B, Sleegers K, Rosso SM, Van den Broeck M, Backhovens H, van Swieten J, van Duijn CM, Van Broeckhoven C. Mol Psychiatry; 2002 Jan; 7(10):1064-74. PubMed ID: 12476321 [Abstract] [Full Text] [Related]
5. Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21. Froelich S, Houlden H, Rizzu P, Chakraverty S, Baker M, Kwon J, Nowotny P, Isaacs A, Nowotny V, Wauters E, van Baren MJ, Oostra BA, Hardy J, Lannfelt L, Goate A, Hutton M, Lendon CL, Heutink P. Genomics; 1999 Sep 01; 60(2):129-36. PubMed ID: 10486204 [Abstract] [Full Text] [Related]
6. [Molecular analysis of tau deposited in the FTDP-17 brain]. Morishima-Kawashima M. Rinsho Shinkeigaku; 2001 Dec 01; 41(12):1107-10. PubMed ID: 12235810 [Abstract] [Full Text] [Related]
7. Contrasting genotypes of the tau gene in two phenotypically distinct patients with P301L mutation of frontotemporal dementia and parkinsonism linked to chromosome 17. Kobayashi T, Mori H, Okuma Y, Dickson DW, Cookson N, Tsuboi Y, Motoi Y, Tanaka R, Miyashita N, Anno M, Narabayashi H, Mizuno Y. J Neurol; 2002 Jun 01; 249(6):669-75. PubMed ID: 12111297 [Abstract] [Full Text] [Related]
8. 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 10; 64(9):1578-85. PubMed ID: 15883319 [Abstract] [Full Text] [Related]
9. 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. PubMed ID: 16862115 [Abstract] [Full Text] [Related]
10. Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation. Boeve BF, Tremont-Lukats IW, Waclawik AJ, Murrell JR, Hermann B, Jack CR, Shiung MM, Smith GE, Nair AR, Lindor N, Koppikar V, Ghetti B. Brain; 2005 Apr 24; 128(Pt 4):752-72. PubMed ID: 15615814 [Abstract] [Full Text] [Related]
13. [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 24; 55(2):107-19. PubMed ID: 12684990 [Abstract] [Full Text] [Related]