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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1994 1
1995 3
1996 4
1998 3
1999 9
2000 2
2001 3
2002 4
2003 1
2004 7
2005 7
2006 3
2007 3
2008 2
2009 6
2010 4
2011 2
2012 3
2013 4
2014 1
2015 2
2016 2
2017 3
2018 1
2021 3
2022 3
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80 results
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Page 1
Animal prion diseases.
Windl O, Dawson M. Windl O, et al. Subcell Biochem. 2012;65:497-516. doi: 10.1007/978-94-007-5416-4_18. Subcell Biochem. 2012. PMID: 23225014 Review.
Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, Ruf V, Windl O, Capellari S, Parchi P. Baiardi S, et al. Among authors: windl o. Acta Neuropathol. 2021 Oct;142(4):707-728. doi: 10.1007/s00401-021-02350-y. Epub 2021 Jul 29. Acta Neuropathol. 2021. PMID: 34324063 Free PMC article.
Latrogenic Creutzfeldt-Jakob disease with florid plaques.
Kretzschmar HA, Sethi S, Földvári Z, Windl O, Querner V, Zerr I, Poser S. Kretzschmar HA, et al. Among authors: windl o. Brain Pathol. 2003 Jul;13(3):245-9. doi: 10.1111/j.1750-3639.2003.tb00025.x. Brain Pathol. 2003. PMID: 12946015 Free PMC article. Review.
Seizure prevalence in neurodegenerative diseases-a study of autopsy proven cases.
Vöglein J, Kostova I, Arzberger T, Noachtar S, Dieterich M, Herms J, Schmitz P, Ruf V, Windl O, Roeber S, Simons M, Höglinger GU, Danek A, Giese A, Levin J. Vöglein J, et al. Among authors: windl o. Eur J Neurol. 2022 Jan;29(1):12-18. doi: 10.1111/ene.15089. Epub 2021 Sep 17. Eur J Neurol. 2022. PMID: 34472165
Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges.
Abu-Rumeileh S, Redaelli V, Baiardi S, Mackenzie G, Windl O, Ritchie DL, Didato G, Hernandez-Vara J, Rossi M, Capellari S, Imperiale D, Rizzone MG, Belotti A, Sorbi S, Rozemuller AJM, Cortelli P, Gelpi E, Will RG, Zerr I, Giaccone G, Parchi P. Abu-Rumeileh S, et al. Among authors: windl o. Ann Neurol. 2018 Sep;84(3):347-360. doi: 10.1002/ana.25300. Epub 2018 Aug 31. Ann Neurol. 2018. PMID: 30048013 Free article.
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: windl o. 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.
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: windl o. Arch Neurol. 1999 Jan;56(1):55-61. doi: 10.1001/archneur.56.1.55. Arch Neurol. 1999. PMID: 9923761
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementia.
Fanciulli A, Leys F, Lehner F, Sidoroff V, Ruf VC, Raccagni C, Mahlknecht P, Kuipers DJS, van IJcken WFJ, Stockner H, Musacchio T, Volkmann J, Monoranu CM, Stankovic I, Breedveld G, Ferraro F, Fevga C, Windl O, Herms J, Kiechl S, Poewe W, Seppi K, Stefanova N, Scholz SW, Bonifati V, Wenning GK. Fanciulli A, et al. Among authors: windl o. Brain Commun. 2022 Jul 4;4(4):fcac175. doi: 10.1093/braincomms/fcac175. eCollection 2022. Brain Commun. 2022. PMID: 35855480 Free PMC article.
Ovine PRNP untranslated region and promoter haplotype diversity.
Saunders GC, Cawthraw S, Mountjoy SJ, Tout AC, Sayers AR, Hope J, Windl O. Saunders GC, et al. Among authors: windl o. J Gen Virol. 2009 May;90(Pt 5):1289-1293. doi: 10.1099/vir.0.007997-0. Epub 2009 Mar 4. J Gen Virol. 2009. PMID: 19264598
80 results