Neumann M - Search Results

1

TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD.

Roeber S, Mackenzie IR, Kretzschmar HA, Neumann M. Roeber S, et al. Among authors: neumann m. Acta Neuropathol. 2008 Aug;116(2):147-57. doi: 10.1007/s00401-008-0395-x. Epub 2008 Jun 7. Acta Neuropathol. 2008. PMID: 18536926

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

RNA aptamers specifically interact with the prion protein PrP.

Weiss S, Proske D, Neumann M, Groschup MH, Kretzschmar HA, Famulok M, Winnacker EL. Weiss S, et al. Among authors: neumann m. J Virol. 1997 Nov;71(11):8790-7. doi: 10.1128/JVI.71.11.8790-8797.1997. J Virol. 1997. PMID: 9343239 Free PMC article.

5

Decreased beta-amyloid1-42 in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.

Otto M, Esselmann H, Schulz-Shaeffer W, Neumann M, Schröter A, Ratzka P, Cepek L, Zerr I, Steinacker P, Windl O, Kornhuber J, Kretzschmar HA, Poser S, Wiltfang J. Otto M, et al. Among authors: neumann m. Neurology. 2000 Mar 14;54(5):1099-102. doi: 10.1212/wnl.54.5.1099. Neurology. 2000. PMID: 10720281

6

Subcellular localization of wild-type and Parkinson's disease-associated mutant alpha -synuclein in human and transgenic mouse brain.

Kahle PJ, Neumann M, Ozmen L, Muller V, Jacobsen H, Schindzielorz A, Okochi M, Leimer U, van Der Putten H, Probst A, Kremmer E, Kretzschmar HA, Haass C. Kahle PJ, et al. Among authors: neumann m. J Neurosci. 2000 Sep 1;20(17):6365-73. doi: 10.1523/JNEUROSCI.20-17-06365.2000. J Neurosci. 2000. PMID: 10964942 Free PMC article.

7

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

8

[Your help is needed! Autopsy brings new knowledge regarding Alzheimer dementia].

Bürger K, Hampel H, Neumann M, Möller HJ, Kretzschmar H. Bürger K, et al. Among authors: neumann m. MMW Fortschr Med. 2000 Sep 28;142(39):40-1. MMW Fortschr Med. 2000. PMID: 11072696 German.

9

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.

10

[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.

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