Windl O - Search Results

1

Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.

Nicholl D, Windl O, de Silva R, Sawcer S, Dempster M, Ironside JW, Estibeiro JP, Yuill GM, Lathe R, Will RG. Nicholl D, et al. Among authors: windl o. J Neurol Neurosurg Psychiatry. 1995 Jan;58(1):65-9. doi: 10.1136/jnnp.58.1.65. J Neurol Neurosurg Psychiatry. 1995. PMID: 7823070 Free PMC article.

2

Neuropathological phenotype and 'prion protein' genotype correlation in sporadic Creutzfeldt-Jakob disease.

de Silva R, Ironside JW, McCardle L, Esmonde T, Bell J, Will R, Windl O, Dempster M, Estibeiro P, Lathe R. de Silva R, et al. Among authors: windl o. Neurosci Lett. 1994 Sep 26;179(1-2):50-2. doi: 10.1016/0304-3940(94)90932-6. Neurosci Lett. 1994. PMID: 7845623

3

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.

Windl O, Dempster M, Estibeiro JP, Lathe R, de Silva R, Esmonde T, Will R, Springbett A, Campbell TA, Sidle KC, Palmer MS, Collinge J. Windl O, et al. Hum Genet. 1996 Sep;98(3):259-64. doi: 10.1007/s004390050204. Hum Genet. 1996. PMID: 8707291

4

A candidate marsupial PrP gene reveals two domains conserved in mammalian PrP proteins.

Windl O, Dempster M, Estibeiro P, Lathe R. Windl O, et al. Gene. 1995 Jul 4;159(2):181-6. doi: 10.1016/0378-1119(95)00064-d. Gene. 1995. PMID: 7622046

5

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.

6

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: windl o. Ann Neurol. 1999 Nov;46(5):693-700. Ann Neurol. 1999. PMID: 10970246

7

Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease.

Zerr I, Bodemer M, Gefeller O, Otto M, Poser S, Wiltfang J, Windl O, Kretzschmar HA, Weber T. Zerr I, et al. Among authors: windl o. Ann Neurol. 1998 Jan;43(1):32-40. doi: 10.1002/ana.410430109. Ann Neurol. 1998. PMID: 9450766

8

Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findings.

Meissner B, Körtner K, Bartl M, Jastrow U, Mollenhauer B, Schröter A, Finkenstaedt M, Windl O, Poser S, Kretzschmar HA, Zerr I. Meissner B, et al. Among authors: windl o. Neurology. 2004 Aug 10;63(3):450-6. doi: 10.1212/01.wnl.0000136225.80445.c9. Neurology. 2004. PMID: 15314808

9

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

10

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.

Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar H. Parchi P, et al. Among authors: windl o. Ann Neurol. 1999 Aug;46(2):224-33. Ann Neurol. 1999. PMID: 10443888

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