Neumann M - Search Results

1

An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies.

de Silva R, Lashley T, Strand C, Shiarli AM, Shi J, Tian J, Bailey KL, Davies P, Bigio EH, Arima K, Iseki E, Murayama S, Kretzschmar H, Neumann M, Lippa C, Halliday G, MacKenzie J, Ravid R, Dickson D, Wszolek Z, Iwatsubo T, Pickering-Brown SM, Holton J, Lees A, Revesz T, Mann DM. de Silva R, et al. Among authors: neumann m. Acta Neuropathol. 2006 Apr;111(4):329-40. doi: 10.1007/s00401-006-0048-x. Epub 2006 Mar 22. Acta Neuropathol. 2006. PMID: 16552612

2

Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72-year-old celloidin-embedded brain tissue.

Kretzschmar HA, Neumann M, Stavrou D. Kretzschmar HA, et al. Among authors: neumann m. Acta Neuropathol. 1995;89(1):96-8. doi: 10.1007/BF00294264. Acta Neuropathol. 1995. PMID: 7709737

3

Alpha-synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies.

Neumann M, Adler S, Schlüter O, Kremmer E, Benecke R, Kretzschmar HA. Neumann M, et al. Acta Neuropathol. 2000 Nov;100(5):568-74. doi: 10.1007/s004010000224. Acta Neuropathol. 2000. PMID: 11045680

4

A pathogenic presenilin-1 deletion causes abberrant Abeta 42 production in the absence of congophilic amyloid plaques.

Steiner H, Revesz T, Neumann M, Romig H, Grim MG, Pesold B, Kretzschmar HA, Hardy J, Holton JL, Baumeister R, Houlden H, Haass C. Steiner H, et al. Among authors: neumann m. J Biol Chem. 2001 Mar 9;276(10):7233-9. doi: 10.1074/jbc.M007183200. Epub 2000 Nov 17. J Biol Chem. 2001. PMID: 11084029 Free article.

5

[Neuropathological diagnosis of neurodegenerative and dementia diseases].

Kretzschmar HA, Neumann M. Kretzschmar HA, et al. Among authors: neumann m. Pathologe. 2000 Sep;21(5):364-74. doi: 10.1007/s002920000402. Pathologe. 2000. PMID: 11092009 German.

6

Pick's disease associated with the novel Tau gene mutation K369I.

Neumann M, Schulz-Schaeffer W, Crowther RA, Smith MJ, Spillantini MG, Goedert M, Kretzschmar HA. Neumann M, et al. Ann Neurol. 2001 Oct;50(4):503-13. doi: 10.1002/ana.1223. Ann Neurol. 2001. PMID: 11601501

7

Hyperphosphorylation and insolubility of alpha-synuclein in transgenic mouse oligodendrocytes.

Kahle PJ, Neumann M, Ozmen L, Muller V, Jacobsen H, Spooren W, Fuss B, Mallon B, Macklin WB, Fujiwara H, Hasegawa M, Iwatsubo T, Kretzschmar HA, Haass C. Kahle PJ, et al. Among authors: neumann m. EMBO Rep. 2002 Jun;3(6):583-8. doi: 10.1093/embo-reports/kvf109. Epub 2002 May 24. EMBO Rep. 2002. PMID: 12034752 Free PMC article.

8

Structure/function of alpha-synuclein in health and disease: rational development of animal models for Parkinson's and related diseases.

Kahle PJ, Haass C, Kretzschmar HA, Neumann M. Kahle PJ, et al. Among authors: neumann m. J Neurochem. 2002 Aug;82(3):449-57. doi: 10.1046/j.1471-4159.2002.01020.x. J Neurochem. 2002. PMID: 12153470 Free article. Review. No abstract available.

9

Misfolded proteinase K-resistant hyperphosphorylated alpha-synuclein in aged transgenic mice with locomotor deterioration and in human alpha-synucleinopathies.

Neumann M, Kahle PJ, Giasson BI, Ozmen L, Borroni E, Spooren W, Müller V, Odoy S, Fujiwara H, Hasegawa M, Iwatsubo T, Trojanowski JQ, Kretzschmar HA, Haass C. Neumann M, et al. J Clin Invest. 2002 Nov;110(10):1429-39. doi: 10.1172/JCI15777. J Clin Invest. 2002. PMID: 12438441 Free PMC article.

10

Pathological properties of the Parkinson's disease-associated protein DJ-1 in alpha-synucleinopathies and tauopathies: relevance for multiple system atrophy and Pick's disease.

Neumann M, Müller V, Görner K, Kretzschmar HA, Haass C, Kahle PJ. Neumann M, et al. Acta Neuropathol. 2004 Jun;107(6):489-96. doi: 10.1007/s00401-004-0834-2. Epub 2004 Feb 26. Acta Neuropathol. 2004. PMID: 14991385

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