Schulz-Schaeffer WJ - Search Results

1

Sporadic Creutzfeldt-Jakob disease with mesiotemporal hypermetabolism.

Euskirchen P, Buchert R, Koch A, Schulz-Schaeffer WJ, Schreiber SJ, Sobesky J. Euskirchen P, et al. J Neurol Sci. 2014 Oct 15;345(1-2):278-80. doi: 10.1016/j.jns.2014.07.054. Epub 2014 Aug 1. J Neurol Sci. 2014. PMID: 25115503 No abstract available.

2

Prion type 2 selection in sporadic Creutzfeldt-Jakob disease affecting peripheral ganglia.

Hofmann A, Wrede A, Jürgens-Wemheuer WM, Schulz-Schaeffer WJ. Hofmann A, et al. Among authors: schulz schaeffer wj. Acta Neuropathol Commun. 2021 Nov 24;9(1):187. doi: 10.1186/s40478-021-01286-4. Acta Neuropathol Commun. 2021. PMID: 34819156 Free PMC article.

3

How to improve the clinical diagnosis of Creutzfeldt-Jakob disease.

Poser S, Mollenhauer B, Kraubeta A, Zerr I, Steinhoff BJ, Schroeter A, Finkenstaedt M, Schulz-Schaeffer WJ, Kretzschmar HA, Felgenhauer K. Poser S, et al. Brain. 1999 Dec;122 ( Pt 12):2345-51. doi: 10.1093/brain/122.12.2345. Brain. 1999. PMID: 10581227

4

Wemheuer WM, Benestad SL, Wrede A, Schulze-Sturm U, Wemheuer WE, Hahmann U, Gawinecka J, Schütz E, Zerr I, Brenig B, Bratberg B, Andréoletti O, Schulz-Schaeffer WJ. Wemheuer WM, et al. Am J Pathol. 2009 Dec;175(6):2566-73. doi: 10.2353/ajpath.2009.090623. Epub 2009 Oct 22. Am J Pathol. 2009. PMID: 19850886 Free PMC article.

5

Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type.

Meissner B, Westner IM, Kallenberg K, Krasnianski A, Bartl M, Varges D, Bösenberg C, Kretzschmar HA, Knauth M, Schulz-Schaeffer WJ, Zerr I. Meissner B, et al. Neurology. 2005 Nov 22;65(10):1544-50. doi: 10.1212/01.wnl.0000184674.32924.c9. Epub 2005 Oct 12. Neurology. 2005. PMID: 16221949

6

Clinical features and diagnosis of the MM2 cortical subtype of sporadic Creutzfeldt-Jakob disease.

Krasnianski A, Meissner B, Schulz-Schaeffer W, Kallenberg K, Bartl M, Heinemann U, Varges D, Kretzschmar HA, Zerr I. Krasnianski A, et al. Arch Neurol. 2006 Jun;63(6):876-80. doi: 10.1001/archneur.63.6.876. Arch Neurol. 2006. PMID: 16769870

7

Neuropsychological Symptoms in Sporadic Creutzfeldt-Jakob Disease Patients in Germany.

Krasnianski A, Bohling GT, Heinemann U, Varges D, Meissner B, Schulz-Schaeffer WJ, Reif A, Zerr I. Krasnianski A, et al. J Alzheimers Dis. 2017;59(1):329-337. doi: 10.3233/JAD-161129. J Alzheimers Dis. 2017. PMID: 28598840

8

Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variants.

Zerr I, Schulz-Schaeffer WJ, Giese A, Bodemer M, Schröter A, Henkel K, Tschampa HJ, Windl O, Pfahlberg A, Steinhoff BJ, Gefeller O, Kretzschmar HA, Poser S. Zerr I, et al. Ann Neurol. 2000 Sep;48(3):323-9. Ann Neurol. 2000. PMID: 10976638

9

Movement disturbances in the differential diagnosis of Creutzfeldt-Jakob disease.

Edler J, Mollenhauer B, Heinemann U, Varges D, Werner C, Zerr I, Schulz-Schaeffer WJ. Edler J, et al. Mov Disord. 2009 Feb 15;24(3):350-6. doi: 10.1002/mds.22253. Mov Disord. 2009. PMID: 19053051

10

Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease.

Schulz-Schaeffer WJ, Giese A, Windl O, Kretzschmar HA. Schulz-Schaeffer WJ, et al. Clin Neuropathol. 1996 Nov-Dec;15(6):353-7. Clin Neuropathol. 1996. PMID: 8937783

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