Roeber S - Search Results

1

A new subtype of frontotemporal lobar degeneration with FUS pathology.

Neumann M, Rademakers R, Roeber S, Baker M, Kretzschmar HA, Mackenzie IR. Neumann M, et al. Among authors: roeber s. Brain. 2009 Nov;132(Pt 11):2922-31. doi: 10.1093/brain/awp214. Epub 2009 Aug 11. Brain. 2009. PMID: 19674978 Free PMC article.

2

Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.

Roeber S, Krebs B, Neumann M, Windl O, Zerr I, Grasbon-Frodl EM, Kretzschmar HA. Roeber S, et al. Acta Neuropathol. 2005 Apr;109(4):443-8. doi: 10.1007/s00401-004-0978-0. Epub 2005 Mar 1. Acta Neuropathol. 2005. PMID: 15739100

3

Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJD.

Krasnianski A, Schulz-Schaeffer WJ, Kallenberg K, Meissner B, Collie DA, Roeber S, Bartl M, Heinemann U, Varges D, Kretzschmar HA, Zerr I. Krasnianski A, et al. Among authors: roeber s. Brain. 2006 Sep;129(Pt 9):2288-96. doi: 10.1093/brain/awl123. Epub 2006 May 23. Brain. 2006. PMID: 16720682

4

Neurodegeneration with features of NIFID and ALS--extended clinical and neuropathological spectrum.

Roeber S, Bäzner H, Hennerici M, Porstmann R, Kretzschmar HA. Roeber S, et al. Brain Pathol. 2006 Jul;16(3):228-34. doi: 10.1111/j.1750-3639.2006.00013.x. Brain Pathol. 2006. PMID: 16911480 Free PMC article.

5

Detection of bone marrow-derived cells expressing a neural phenotype in the human brain.

Sostak P, Theil D, Stepp H, Roeber S, Kretzschmar HA, Straube A. Sostak P, et al. Among authors: roeber s. J Neuropathol Exp Neurol. 2007 Feb;66(2):110-6. doi: 10.1097/nen.0b013e3180301be8. J Neuropathol Exp Neurol. 2007. PMID: 17278995

6

Evidence for a pathogenic role of different mutations at codon 188 of PRNP.

Roeber S, Grasbon-Frodl EM, Windl O, Krebs B, Xiang W, Vollmert C, Illig T, Schröter A, Arzberger T, Weber P, Zerr I, Kretzschmar HA. Roeber S, et al. PLoS One. 2008 May 14;3(5):e2147. doi: 10.1371/journal.pone.0002147. PLoS One. 2008. PMID: 18478114 Free PMC article.

7

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. Acta Neuropathol. 2008 Aug;116(2):147-57. doi: 10.1007/s00401-008-0395-x. Epub 2008 Jun 7. Acta Neuropathol. 2008. PMID: 18536926

8

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease.

Neumann M, Roeber S, Kretzschmar HA, Rademakers R, Baker M, Mackenzie IR. Neumann M, et al. Among authors: roeber s. Acta Neuropathol. 2009 Nov;118(5):605-16. doi: 10.1007/s00401-009-0581-5. Epub 2009 Aug 9. Acta Neuropathol. 2009. PMID: 19669651 Free PMC article.

9

Distinct pathological subtypes of FTLD-FUS.

Mackenzie IR, Munoz DG, Kusaka H, Yokota O, Ishihara K, Roeber S, Kretzschmar HA, Cairns NJ, Neumann M. Mackenzie IR, et al. Among authors: roeber s. Acta Neuropathol. 2011 Feb;121(2):207-18. doi: 10.1007/s00401-010-0764-0. Epub 2010 Oct 30. Acta Neuropathol. 2011. PMID: 21052700

10

Different CSF β-amyloid processing in Alzheimer's and Creutzfeldt-Jakob disease.

Mollenhauer B, Esselmann H, Roeber S, Schulz-Schaeffer WJ, Trenkwalder C, Bibl M, Steinacker P, Kretzschmar HA, Wiltfang J, Otto M. Mollenhauer B, et al. Among authors: roeber s. J Neural Transm (Vienna). 2011 May;118(5):691-7. doi: 10.1007/s00702-010-0543-z. Epub 2011 Jan 6. J Neural Transm (Vienna). 2011. PMID: 21210287

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