Neumann M - Search Results

1

TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

Steinacker P, Hendrich C, Sperfeld AD, Jesse S, von Arnim CA, Lehnert S, Pabst A, Uttner I, Tumani H, Lee VM, Trojanowski JQ, Kretzschmar HA, Ludolph A, Neumann M, Otto M. Steinacker P, et al. Among authors: neumann m. Arch Neurol. 2008 Nov;65(11):1481-7. doi: 10.1001/archneur.65.11.1481. Arch Neurol. 2008. PMID: 19001167 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

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

5

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

6

[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.

7

Decreased CSF amyloid beta42 and normal tau levels in dementia with Lewy bodies.

Tschampa HJ, Schulz-Schaeffer W, Wiltfang J, Poser S, Otto M, Neumann M, Kretzschmar HA. Tschampa HJ, et al. Among authors: neumann m. Neurology. 2001 Feb 27;56(4):576. doi: 10.1212/wnl.56.4.576. Neurology. 2001. PMID: 11222819 No abstract available.

8

Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob disease.

Tschampa HJ, Neumann M, Zerr I, Henkel K, Schröter A, Schulz-Schaeffer WJ, Steinhoff BJ, Kretzschmar HA, Poser S. Tschampa HJ, et al. Among authors: neumann m. J Neurol Neurosurg Psychiatry. 2001 Jul;71(1):33-9. doi: 10.1136/jnnp.71.1.33. J Neurol Neurosurg Psychiatry. 2001. PMID: 11413259 Free PMC article.

9

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

10

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.

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