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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 1
1986 3
1987 2
1989 2
1990 2
1991 4
1992 2
1993 5
1994 4
1995 7
1996 12
1997 14
1998 11
1999 14
2000 18
2001 17
2002 11
2003 5
2004 20
2005 26
2006 18
2007 30
2008 26
2009 19
2010 9
2011 20
2012 16
2013 14
2014 10
2015 12
2016 3
2017 1
2018 1
2021 0
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331 results
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Page 1
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, Bruce J, Schuck T, Grossman M, Clark CM, McCluskey LF, Miller BL, Masliah E, Mackenzie IR, Feldman H, Feiden W, Kretzschmar HA, Trojanowski JQ, Lee VM. Neumann M, et al. Among authors: kretzschmar ha. Science. 2006 Oct 6;314(5796):130-3. doi: 10.1126/science.1134108. Science. 2006. PMID: 17023659 Free article.
DNA methylation analysis on purified neurons and glia dissects age and Alzheimer's disease-specific changes in the human cortex.
Gasparoni G, Bultmann S, Lutsik P, Kraus TFJ, Sordon S, Vlcek J, Dietinger V, Steinmaurer M, Haider M, Mulholland CB, Arzberger T, Roeber S, Riemenschneider M, Kretzschmar HA, Giese A, Leonhardt H, Walter J. Gasparoni G, et al. Among authors: kretzschmar ha. Epigenetics Chromatin. 2018 Jul 25;11(1):41. doi: 10.1186/s13072-018-0211-3. Epigenetics Chromatin. 2018. PMID: 30045751 Free PMC article.
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids.
Rademakers R, Baker M, Nicholson AM, Rutherford NJ, Finch N, Soto-Ortolaza A, Lash J, Wider C, Wojtas A, DeJesus-Hernandez M, Adamson J, Kouri N, Sundal C, Shuster EA, Aasly J, MacKenzie J, Roeber S, Kretzschmar HA, Boeve BF, Knopman DS, Petersen RC, Cairns NJ, Ghetti B, Spina S, Garbern J, Tselis AC, Uitti R, Das P, Van Gerpen JA, Meschia JF, Levy S, Broderick DF, Graff-Radford N, Ross OA, Miller BB, Swerdlow RH, Dickson DW, Wszolek ZK. Rademakers R, et al. Among authors: kretzschmar ha. Nat Genet. 2011 Dec 25;44(2):200-5. doi: 10.1038/ng.1027. Nat Genet. 2011. PMID: 22197934 Free PMC article.
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
Mackenzie IR, Bigio EH, Ince PG, Geser F, Neumann M, Cairns NJ, Kwong LK, Forman MS, Ravits J, Stewart H, Eisen A, McClusky L, Kretzschmar HA, Monoranu CM, Highley JR, Kirby J, Siddique T, Shaw PJ, Lee VM, Trojanowski JQ. Mackenzie IR, et al. Among authors: kretzschmar ha. Ann Neurol. 2007 May;61(5):427-34. doi: 10.1002/ana.21147. Ann Neurol. 2007. PMID: 17469116
Diagnosis of prion diseases.
Kretzschmar HA. Kretzschmar HA. Clin Lab Med. 2003 Mar;23(1):109-28, viii. doi: 10.1016/s0272-2712(02)00043-4. Clin Lab Med. 2003. PMID: 12733427 Review.
[German consortium for frontotemporal lobar degeneration].
Otto M, Ludolph AC, Landwehrmeyer B, Förstl H, Diehl-Schmid J, Neumann M, Kretzschmar HA, Schroeter M, Kornhuber J, Danek A; FTLD consortium. Otto M, et al. Among authors: kretzschmar ha. Nervenarzt. 2011 Aug;82(8):1002-5. doi: 10.1007/s00115-011-3261-3. Nervenarzt. 2011. PMID: 21805118 Review. German.
Cell death in prion disease.
Kretzschmar HA, Giese A, Brown DR, Herms J, Keller B, Schmidt B, Groschup M. Kretzschmar HA, et al. J Neural Transm Suppl. 1997;50:191-210. doi: 10.1007/978-3-7091-6842-4_19. J Neural Transm Suppl. 1997. PMID: 9120419 Review.
Molecular pathogenesis of prion diseases.
Kretzschmar HA. Kretzschmar HA. Eur Arch Psychiatry Clin Neurosci. 1999;249 Suppl 3:56-63. doi: 10.1007/pl00014175. Eur Arch Psychiatry Clin Neurosci. 1999. PMID: 10654101 Review.
331 results
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