Schulz-Schaeffer WJ - Search Results

1

Spongiform encephalopathy in siblings with no evidence of protease-resistant prion protein or a mutation in the prion protein gene.

Varges D, Schulz-Schaeffer WJ, Wemheuer WM, Damman I, Schmitz M, Cramm M, Kallenberg K, Shirneshan K, Elkenani M, Markwort S, Faist M, Kohlhase J, Windl O, Zerr I. Varges D, et al. J Neurol. 2013 Jul;260(7):1871-9. doi: 10.1007/s00415-013-6897-z. Epub 2013 Apr 2. J Neurol. 2013. PMID: 23546304

2

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. Brain. 2006 Sep;129(Pt 9):2288-96. doi: 10.1093/brain/awl123. Epub 2006 May 23. Brain. 2006. PMID: 16720682

3

Filtration of protein aggregates increases the accuracy for diagnosing prion diseases in brain biopsies.

Wemheuer WM, Wrede A, Gawinecka J, Zerr I, Schulz-Schaeffer WJ. Wemheuer WM, et al. J Neuropathol Exp Neurol. 2013 Aug;72(8):758-67. doi: 10.1097/NEN.0b013e31829d2799. J Neuropathol Exp Neurol. 2013. PMID: 23860029 Free article.

4

Validation and utilization of amended diagnostic criteria in Creutzfeldt-Jakob disease surveillance.

Hermann P, Laux M, Glatzel M, Matschke J, Knipper T, Goebel S, Treig J, Schulz-Schaeffer W, Cramm M, Schmitz M, Zerr I. Hermann P, et al. Neurology. 2018 Jul 24;91(4):e331-e338. doi: 10.1212/WNL.0000000000005860. Epub 2018 Jun 22. Neurology. 2018. PMID: 29934424

5

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

6

Clinical findings in sporadic Creutzfeldt-Jakob disease correlate with thalamic pathology.

Tschampa HJ, Herms JW, Schulz-Schaeffer WJ, Maruschak B, Windl O, Jastrow U, Zerr I, Steinhoff BJ, Poser S, Kretzschmar HA. Tschampa HJ, et al. Brain. 2002 Nov;125(Pt 11):2558-66. doi: 10.1093/brain/awf253. Brain. 2002. PMID: 12390980

7

Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

Boesenberg C, Schulz-Schaeffer WJ, Meissner B, Kallenberg K, Bartl M, Heinemann U, Krasnianski A, Stoeck K, Varges D, Windl O, Kretzschmar HA, Zerr I. Boesenberg C, et al. Ann Neurol. 2005 Oct;58(4):533-43. doi: 10.1002/ana.20568. Ann Neurol. 2005. PMID: 16037975

8

Brain-derived proteins in the CSF: do they correlate with brain pathology in CJD?

Boesenberg-Grosse C, Schulz-Schaeffer WJ, Bodemer M, Ciesielczyk B, Meissner B, Krasnianski A, Bartl M, Heinemann U, Varges D, Eigenbrod S, Kretzschmar HA, Green A, Zerr I. Boesenberg-Grosse C, et al. BMC Neurol. 2006 Sep 21;6:35. doi: 10.1186/1471-2377-6-35. BMC Neurol. 2006. PMID: 16989662 Free PMC article.

9

Fatal familial insomnia: Clinical features and early identification.

Krasnianski A, Bartl M, Sanchez Juan PJ, Heinemann U, Meissner B, Varges D, Schulze-Sturm U, Kretzschmar HA, Schulz-Schaeffer WJ, Zerr I. Krasnianski A, et al. Ann Neurol. 2008 May;63(5):658-61. doi: 10.1002/ana.21358. Ann Neurol. 2008. PMID: 18360821

10

Cellular prion protein directly interacts with and enhances lactate dehydrogenase expression under hypoxic conditions.

Ramljak S, Schmitz M, Zafar S, Wrede A, Schenkel S, Asif AR, Carimalo J, Doeppner TR, Schulz-Schaeffer WJ, Weise J, Zerr I. Ramljak S, et al. Exp Neurol. 2015 Sep;271:155-67. doi: 10.1016/j.expneurol.2015.04.025. Epub 2015 May 27. Exp Neurol. 2015. PMID: 26024859

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