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
321 related items for PubMed ID: 11117541
1. Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation. Lippa CF, Zhukareva V, Kawarai T, Uryu K, Shafiq M, Nee LE, Grafman J, Liang Y, St George-Hyslop PH, Trojanowski JQ, Lee VM. Ann Neurol; 2000 Dec; 48(6):850-8. PubMed ID: 11117541 [Abstract] [Full Text] [Related]
3. The DeltaK280 mutation in MAP tau favors exon 10 skipping in vivo. van Swieten JC, Bronner IF, Azmani A, Severijnen LA, Kamphorst W, Ravid R, Rizzu P, Willemsen R, Heutink P. J Neuropathol Exp Neurol; 2007 Jan; 66(1):17-25. PubMed ID: 17204933 [Abstract] [Full Text] [Related]
4. The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy. Hogg M, Grujic ZM, Baker M, Demirci S, Guillozet AL, Sweet AP, Herzog LL, Weintraub S, Mesulam MM, LaPointe NE, Gamblin TC, Berry RW, Binder LI, de Silva R, Lees A, Espinoza M, Davies P, Grover A, Sahara N, Ishizawa T, Dickson D, Yen SH, Hutton M, Bigio EH. Acta Neuropathol; 2003 Oct; 106(4):323-36. PubMed ID: 12883828 [Abstract] [Full Text] [Related]
6. A new family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects. Neumann M, Mittelbronn M, Simon P, Vanmassenhove B, de Silva R, Lees A, Klapp J, Meyermann R, Kretzschmar HA. Neuropathol Appl Neurobiol; 2005 Aug; 31(4):362-73. PubMed ID: 16008820 [Abstract] [Full Text] [Related]
7. Frontotemporal dementia with Pick-type histology associated with Q336R mutation in the tau gene. Pickering-Brown SM, Baker M, Nonaka T, Ikeda K, Sharma S, Mackenzie J, Simpson SA, Moore JW, Snowden JS, de Silva R, Revesz T, Hasegawa M, Hutton M, Mann DM. Brain; 2004 Jun; 127(Pt 6):1415-26. PubMed ID: 15047590 [Abstract] [Full Text] [Related]
8. 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]
9. A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology. Kobayashi T, Ota S, Tanaka K, Ito Y, Hasegawa M, Umeda Y, Motoi Y, Takanashi M, Yasuhara M, Anno M, Mizuno Y, Mori H. Ann Neurol; 2003 Jan; 53(1):133-7. PubMed ID: 12509859 [Abstract] [Full Text] [Related]
13. 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]
16. [The genetics of dementias. Part 1: Molecular basis of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)]. Kowalska A. Postepy Hig Med Dosw (Online); 2009 Jun 15; 63():278-86. PubMed ID: 19535823 [Abstract] [Full Text] [Related]
17. 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 15; 249(6):669-75. PubMed ID: 12111297 [Abstract] [Full Text] [Related]
19. Tau gene mutations and their effects. Goedert M. Mov Disord; 2005 Aug 15; 20 Suppl 12():S45-52. PubMed ID: 16092090 [Abstract] [Full Text] [Related]
20. Total tau and phosphorylated tau 181 levels in the cerebrospinal fluid of patients with frontotemporal dementia due to P301L and G272V tau mutations. Rosso SM, van Herpen E, Pijnenburg YA, Schoonenboom NS, Scheltens P, Heutink P, van Swieten JC. Arch Neurol; 2003 Sep 15; 60(9):1209-13. PubMed ID: 12975285 [Abstract] [Full Text] [Related] Page: [Next] [New Search]