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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: zerr i. Brain. 2006 Sep;129(Pt 9):2288-96. doi: 10.1093/brain/awl123. Epub 2006 May 23. Brain. 2006. PMID: 16720682
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. Among authors: zerr i. Ann Neurol. 2008 May;63(5):658-61. doi: 10.1002/ana.21358. Ann Neurol. 2008. PMID: 18360821
MRI and clinical syndrome in dura mater-related Creutzfeldt-Jakob disease.
Meissner B, Kallenberg K, Sanchez-Juan P, Ramljak S, Krasnianski A, Heinemann U, Eigenbrod S, Gelpi E, Barsic B, Kretzschmar HA, Schulz-Schaeffer WJ, Knauth M, Zerr I. Meissner B, et al. Among authors: zerr i. J Neurol. 2009 Mar;256(3):355-63. doi: 10.1007/s00415-009-0026-z. Epub 2009 Jan 23. J Neurol. 2009. PMID: 19159063 Free article.
A proposal of new diagnostic pathway for fatal familial insomnia.
Krasnianski A, Sanchez Juan P, Ponto C, Bartl M, Heinemann U, Varges D, Schulz-Schaeffer WJ, Kretzschmar HA, Zerr I. Krasnianski A, et al. Among authors: zerr i. J Neurol Neurosurg Psychiatry. 2014 Jun;85(6):654-9. doi: 10.1136/jnnp-2013-305978. Epub 2013 Nov 18. J Neurol Neurosurg Psychiatry. 2014. PMID: 24249784 Free PMC article.
Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I. Schmitz M, et al. Among authors: zerr i. Neurobiol Aging. 2014 May;35(5):1177-88. doi: 10.1016/j.neurobiolaging.2013.11.010. Epub 2013 Nov 16. Neurobiol Aging. 2014. PMID: 24360565
409 results