Neumann M - Search Results

1

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies.

Neumann M, Kwong LK, Lee EB, Kremmer E, Flatley A, Xu Y, Forman MS, Troost D, Kretzschmar HA, Trojanowski JQ, Lee VM. Neumann M, et al. Acta Neuropathol. 2009 Feb;117(2):137-49. doi: 10.1007/s00401-008-0477-9. Epub 2009 Jan 6. Acta Neuropathol. 2009. PMID: 19125255 Free PMC article.

2

Molecular cloning of a mink prion protein gene.

Kretzschmar HA, Neumann M, Riethmüller G, Prusiner SB. Kretzschmar HA, et al. Among authors: neumann m. J Gen Virol. 1992 Oct;73 ( Pt 10):2757-61. doi: 10.1099/0022-1317-73-10-2757. J Gen Virol. 1992. PMID: 1383401

3

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

4

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

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

Selective insolubility of alpha-synuclein in human Lewy body diseases is recapitulated in a transgenic mouse model.

Kahle PJ, Neumann M, Ozmen L, Müller V, Odoy S, Okamoto N, Jacobsen H, Iwatsubo T, Trojanowski JQ, Takahashi H, Wakabayashi K, Bogdanovic N, Riederer P, Kretzschmar HA, Haass C. Kahle PJ, et al. Among authors: neumann m. Am J Pathol. 2001 Dec;159(6):2215-25. doi: 10.1016/s0002-9440(10)63072-6. Am J Pathol. 2001. PMID: 11733371 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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