Zerr I - Search Results

1

Deletion of cellular prion protein results in reduced Akt activation, enhanced postischemic caspase-3 activation, and exacerbation of ischemic brain injury.

Weise J, Sandau R, Schwarting S, Crome O, Wrede A, Schulz-Schaeffer W, Zerr I, Bähr M. Weise J, et al. Among authors: zerr i. Stroke. 2006 May;37(5):1296-300. doi: 10.1161/01.STR.0000217262.03192.d4. Epub 2006 Mar 30. Stroke. 2006. PMID: 16574930

2

The German FFI cases.

Kretzschmar H, Giese A, Zerr I, Windl O, Schulz-Schaeffer W, Skworc K, Poser S. Kretzschmar H, et al. Among authors: zerr i. Brain Pathol. 1998 Jul;8(3):559-61. doi: 10.1111/j.1750-3639.1998.tb00181.x. Brain Pathol. 1998. PMID: 9669710 Free PMC article. No abstract available.

3

Phenotypic variability in fatal familial insomnia (D178N-129M) genotype.

Zerr I, Giese A, Windl O, Kropp S, Schulz-Schaeffer W, Riedemann C, Skworc K, Bodemer M, Kretzschmar HA, Poser S. Zerr I, et al. Neurology. 1998 Nov;51(5):1398-405. doi: 10.1212/wnl.51.5.1398. Neurology. 1998. PMID: 9818868

4

The Heidenhain variant of Creutzfeldt-Jakob disease.

Kropp S, Schulz-Schaeffer WJ, Finkenstaedt M, Riedemann C, Windl O, Steinhoff BJ, Zerr I, Kretzschmar HA, Poser S. Kropp S, et al. Among authors: zerr i. Arch Neurol. 1999 Jan;56(1):55-61. doi: 10.1001/archneur.56.1.55. Arch Neurol. 1999. PMID: 9923761

5

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. Among authors: zerr i. Brain. 1999 Dec;122 ( Pt 12):2345-51. doi: 10.1093/brain/122.12.2345. Brain. 1999. PMID: 10581227

6

Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targets.

Bieschke J, Giese A, Schulz-Schaeffer W, Zerr I, Poser S, Eigen M, Kretzschmar H. Bieschke J, et al. Among authors: zerr i. Proc Natl Acad Sci U S A. 2000 May 9;97(10):5468-73. doi: 10.1073/pnas.97.10.5468. Proc Natl Acad Sci U S A. 2000. PMID: 10805803 Free PMC article.

7

Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene.

Skworc KH, Windl O, Schulz-Schaeffer WJ, Giese A, Bergk J, Nägele A, Vieregge P, Zerr I, Poser S, Kretzschmar HA. Skworc KH, et al. Among authors: zerr i. Ann Neurol. 1999 Nov;46(5):693-700. Ann Neurol. 1999. PMID: 10970246

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

Molecular genetics of human prion diseases in Germany.

Windl O, Giese A, Schulz-Schaeffer W, Zerr I, Skworc K, Arendt S, Oberdieck C, Bodemer M, Poser S, Kretzschmar HA. Windl O, et al. Among authors: zerr i. Hum Genet. 1999 Sep;105(3):244-52. doi: 10.1007/s004399900124. Hum Genet. 1999. PMID: 10987652

10

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. Among authors: zerr i. Brain. 2002 Nov;125(Pt 11):2558-66. doi: 10.1093/brain/awf253. Brain. 2002. PMID: 12390980

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