Zentrum für Neuropathologie und Prionforschung




Dr. rer. nat. Otto Windl

[2023] [2022] [2021] [2018] [2017] [2016] [2015] [2013] [2012] [2011] [2010] [2009] [2008] [2007] [2006] [2005] [2004] [2003] [2002] [2001] [2000] [1999] [1998] [1996] [1995] [1994] [1993]


Tauber CV, Schwarz SC, Rösler TW, Arzberger T, Gentleman S, Windl O, Krumbiegel M, Reis A, Ruf VC, Herms J & Höglinger GU
Different MAPT haplotypes influence expression of total MAPT in postmortem brain tissue.
Acta neuropathologica communications, 2023 Mar 11, 11 (1) 40


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
Seizure prevalence in neurodegenerative diseases-a study of autopsy proven cases.
European journal of neurology, 2022 Jan, 29 (1) 12-18

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
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementia.
Brain communications, 2022, 4 (4) fcac175


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
Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
Acta neuropathologica, 2021 Oct, 142 (4) 707-728

Vöglein J, Kostova I, Arzberger T, Roeber S, Schmitz P, Simons M, Ruf V, Windl O, Herms J, Dieterich M, Danek A, Höglinger GU, Giese A & Levin J
First symptom guides diagnosis and prognosis in neurodegenerative diseases-a retrospective study of autopsy proven cases.
European journal of neurology, 2021 Jun, 28 (6) 1801-1811


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
Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges.
Annals of neurology, 2018 Sep, 84 (3) 347-360


Papasavva-Stylianou P, Simmons MM, Ortiz-Pelaez A, Windl O, Spiropoulos J & Georgiadou S
Effect of Polymorphisms at Codon 146 of the Goat PRNP Gene on Susceptibility to Challenge with Classical Scrapie by Different Routes.
Journal of virology, 2017 Nov 15, 91 (22)

Eigenbrod S, Frick P, Bertsch U, Mitteregger-Kretzschmar G, Mielke J, Maringer M, Piening N, Hepp A, Daude N, Windl O, Levin J, Giese A, Sakthivelu V, Tatzelt J, Kretzschmar H & Westaway D
Substitutions of PrP N-terminal histidine residues modulate scrapie disease pathogenesis and incubation time in transgenic mice.
PloS one, 2017, 12 (12) e0188989

Georgiadou S, Ortiz-Pelaez A, Simmons MM, Windl O, Dawson M, Neocleous P & Papasavva-Stylianou P
Goats with aspartic acid or serine at codon 146 of the PRNP gene remain scrapie-negative after lifetime exposure in affected herds in Cyprus.
Epidemiology and infection, 2017 Jan, 145 (2) 326-328


Goldmann W, Marier E, Stewart P, Konold T, Street S, Langeveld J, Windl O & Ortiz-Pelaez A
Prion protein genotype survey confirms low frequency of scrapie-resistant K222 allele in British goat herds.
The Veterinary record, 2016 Feb 13, 178 (7) 168


Ortiz-Pelaez A, Georgiadou S, Simmons MM, Windl O, Dawson M, Arnold ME, Neocleous P & Papasavva-Stylianou P
Allelic variants at codon 146 in the PRNP gene show significant differences in the risk for natural scrapie in Cypriot goats.
Epidemiology and infection, 2015 Apr, 143 (6) 1304-10

Tark D, Kim H, Neale MH, Kim M, Sohn H, Lee Y, Cho I, Joo Y & Windl O
Generation of a persistently infected MDBK cell line with natural bovine spongiform encephalopathy (BSE).
PloS one, 2015, 10 (2) e0115939


Griffiths PC, Plater JM, Chave A, Jayasena D, Tout AC, Rice PB, Vickery CM, Spiropoulos J, Stack MJ & Windl O
Overexpression of chimaeric murine/ovine PrP (A136H154Q171) in transgenic mice facilitates transmission and differentiation of ruminant prions.
The Journal of general virology, 2013 Nov, 94 (Pt 11) 2577-2586

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
Spongiform encephalopathy in siblings with no evidence of protease-resistant prion protein or a mutation in the prion protein gene.
Journal of neurology, 2013 Jul, 260 (7) 1871-9

Stack MJ, Chaplin MJ, Davis LA, Everitt S, Simmons MM, Windl O, Hope J & Burke P
Four BSE cases with an L-BSE molecular profile in cattle from Great Britain.
The Veterinary record, 2013 Jan 19, 172 (3) 70

Okoroma EA, Purchase D, Garelick H, Morris R, Neale MH, Windl O & Abiola OO
Enzymatic formulation capable of degrading scrapie prion under mild digestion conditions.
PloS one, 2013, 8 (7) e68099


Thorne L, Holder T, Ramsay A, Edwards J, Taema MM, Windl O, Maddison BC, Gough KC & Terry LA
In vitro amplification of ovine prions from scrapie-infected sheep from Great Britain reveals distinct patterns of propagation.
BMC veterinary research, 2012 Nov 15, 8 223

Windl O & Dawson M
Animal prion diseases.
Sub-cellular biochemistry, 2012, 65 497-516


Goldmann W, Ryan K, Stewart P, Parnham D, Xicohtencatl R, Fernandez N, Saunders G, Windl O, González L, Bossers A & Foster J
Caprine prion gene polymorphisms are associated with decreased incidence of classical scrapie in goat herds in the United Kingdom.
Veterinary research, 2011 Oct 31, 42 (1) 110

Papasavva-Stylianou P, Windl O, Saunders G, Mavrikiou P, Toumazos P & Kakoyiannis C
PrP gene polymorphisms in Cyprus goats and their association with resistance or susceptibility to natural scrapie.
Veterinary journal (London, England : 1997), 2011 Feb, 187 (2) 245-50


Tang Y, Xiang W, Terry L, Kretzschmar HA & Windl O
Transcriptional analysis implicates endoplasmic reticulum stress in bovine spongiform encephalopathy.
PloS one, 2010 Dec 03, 5 (12) e14207

Neale MH, Mountjoy SJ, Edwards JC, Vilette D, Laude H, Windl O & Saunders GC
Infection of cell lines with experimental and natural ovine scrapie agents.
Journal of virology, 2010 Mar, 84 (5) 2444-52

Provansal M, Roche S, Pastore M, Casanova D, Belondrade M, Alais S, Leblanc P, Windl O & Lehmann S
Proteomic consequences of expression and pathological conversion of the prion protein in inducible neuroblastoma N2a cells.
Prion, 2010, 4 (4) 292-301


Saunders GC, Lantier I, Cawthraw S, Berthon P, Moore SJ, Arnold ME, Windl O, Simmons MM, Andréoletti O, Bellworthy S & Lantier F
Protective effect of the T112 PrP variant in sheep challenged with bovine spongiform encephalopathy.
The Journal of general virology, 2009 Oct, 90 (Pt 10) 2569-2574

Cawthraw S, Saunders GC, Martin TC, Sawyer J, Windl O & Reaney SD
Real-time PCR detection and identification of prohibited mammalian and avian material in animal feeds.
Journal of food protection, 2009 May, 72 (5) 1055-62

Saunders GC, Cawthraw S, Mountjoy SJ, Tout AC, Sayers AR, Hope J & Windl O
Ovine PRNP untranslated region and promoter haplotype diversity.
The Journal of general virology, 2009 May, 90 (Pt 5) 1289-1293

González L, Martin S, Sisó S, Konold T, Ortiz-Peláez A, Phelan L, Goldmann W, Stewart P, Saunders G, Windl O, Jeffrey M, Hawkins SA, Dawson M & Hope J
High prevalence of scrapie in a dairy goat herd: tissue distribution of disease-associated PrP and effect of PRNP genotype and age.
Veterinary research, 2009, 40 (6) 65


Agrimi U, Nonno R, Dell'Omo G, Di Bari MA, Conte M, Chiappini B, Esposito E, Di Guardo G, Windl O, Vaccari G & Lipp HP
Prion protein amino acid determinants of differential susceptibility and molecular feature of prion strains in mice and voles.
PLoS pathogens, 2008 Jul 25, 4 (7) e1000113

Roeber S, Grasbon-Frodl EM, Windl O, Krebs B, Xiang W, Vollmert C, Illig T, Schröter A, Arzberger T, Weber P, Zerr I & Kretzschmar HA
Evidence for a pathogenic role of different mutations at codon 188 of PRNP.
PloS one, 2008 May 14, 3 (5) e2147


Saunders GC, Horigan V, Tout AC & Windl O
Identification of a proteinase K resistant protein for use as an internal positive control marker in PrP Western blotting.
Research in veterinary science, 2007 Oct, 83 (2) 157-64

Xiang W, Hummel M, Mitteregger G, Pace C, Windl O, Mansmann U & Kretzschmar HA
Transcriptome analysis reveals altered cholesterol metabolism during the neurodegeneration in mouse scrapie model.
Journal of neurochemistry, 2007 Aug, 102 (3) 834-47

Saunders GC, Griffiths PC, Cawthraw S, Tout AC, Wiener P, Woolliams JA, Williams JL & Windl O
Polymorphisms of the prion protein gene coding region in born-after-the-reinforced-ban (BARB) bovine spongiform encephalopathy cattle in Great Britain.
The Journal of general virology, 2007 Apr, 88 (Pt 4) 1374-1378


Saunders GC, Cawthraw S, Mountjoy SJ, Hope J & Windl O
PrP genotypes of atypical scrapie cases in Great Britain.
The Journal of general virology, 2006 Nov, 87 (Pt 11) 3141-3149

Vollmert C, Windl O, Xiang W, Rosenberger A, Zerr I, Wichmann HE, Bickeböller H, Illig T, KORA group & Kretzschmar HA
Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study.
Journal of medical genetics, 2006 Oct, 43 (10) e53

Piening N, Nonno R, Di Bari M, Walter S, Windl O, Agrimi U, Kretzschmar HA & Bertsch U
Conversion efficiency of bank vole prion protein in vitro is determined by residues 155 and 170, but does not correlate with the high susceptibility of bank voles to sheep scrapie in vivo.
The Journal of biological chemistry, 2006 Apr 07, 281 (14) 9373-84


Windl O, Buchholz M, Neubauer A, Schulz-Schaeffer W, Groschup M, Walter S, Arendt S, Neumann M, Voss AK & Kretzschmar HA
Breaking an absolute species barrier: transgenic mice expressing the mink PrP gene are susceptible to transmissible mink encephalopathy.
Journal of virology, 2005 Dec, 79 (23) 14971-5

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
Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.
Annals of neurology, 2005 Oct, 58 (4) 533-43

Xiang W, Windl O, Westner IM, Neumann M, Zerr I, Lederer RM & Kretzschmar HA
Cerebral gene expression profiles in sporadic Creutzfeldt-Jakob disease.
Annals of neurology, 2005 Aug, 58 (2) 242-57

Cartoni C, Schininà ME, Maras B, Nonno R, Vaccari G, Di Baria MA, Conte M, Liu QG, Lu M, Cardone F, Windl O, Pocchiari M & Agrimi U
Identification of the pathological prion protein allotypes in scrapie-infected heterozygous bank voles (Clethrionomys glareolus) by high-performance liquid chromatography-mass spectrometry.
Journal of chromatography. A, 2005 Jul 15, 1081 (1) 122-6

Vassallo N, Herms J, Behrens C, Krebs B, Saeki K, Onodera T, Windl O & Kretzschmar HA
Activation of phosphatidylinositol 3-kinase by cellular prion protein and its role in cell survival.
Biochemical and biophysical research communications, 2005 Jun 24, 332 (1) 75-82

Krebs B, Lederer RM, Windl O, Grasbon-Frodl EM, Zerr I & Kretzschmar HA
Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein gene.
Neurogenetics, 2005 May, 6 (2) 97-100

Roeber S, Krebs B, Neumann M, Windl O, Zerr I, Grasbon-Frodl EM & Kretzschmar HA
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.
Acta neuropathologica, 2005 Apr, 109 (4) 443-8


Drisaldi B, Coomaraswamy J, Mastrangelo P, Strome B, Yang J, Watts JC, Chishti MA, Marvi M, Windl O, Ahrens R, Major F, Sy MS, Kretzschmar H, Fraser PE, Mount HT & Westaway D
Genetic mapping of activity determinants within cellular prion proteins: N-terminal modules in PrPC offset pro-apoptotic activity of the Doppel helix B/B' region.
The Journal of biological chemistry, 2004 Dec 31, 279 (53) 55443-54

Grasbon-Frodl E, Schmalzbauer R, Weber P, Krebs B, Windl O, Zerr I & Kretzschmar HA
A novel three extra-repeat insertion in the prion protein gene (PRNP) in a patient with Creutzfeldt-Jakob disease.
Neurogenetics, 2004 Dec, 5 (4) 249-50

Grasbon-Frodl E, Lorenz H, Mann U, Nitsch RM, Windl O & Kretzschmar HA
Loss of glycosylation associated with the T183A mutation in human prion disease.
Acta neuropathologica, 2004 Dec, 108 (6) 476-84

Xiang W, Windl O, Wünsch G, Dugas M, Kohlmann A, Dierkes N, Westner IM & Kretzschmar HA
Identification of differentially expressed genes in scrapie-infected mouse brains by using global gene expression technology.
Journal of virology, 2004 Oct, 78 (20) 11051-60

Meissner B, Körtner K, Bartl M, Jastrow U, Mollenhauer B, Schröter A, Finkenstaedt M, Windl O, Poser S, Kretzschmar HA & Zerr I
Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findings.
Neurology, 2004 Aug 10, 63 (3) 450-6

Harder A, Gregor A, Wirth T, Kreuz F, Schulz-Schaeffer WJ, Windl O, Plotkin M, Amthauer H, Neukirch K, Kretzschmar HA, Kuhlmann T, Braas R, Hahne HH & Jendroska K
Early age of onset in fatal familial insomnia. Two novel cases and review of the literature.
Journal of neurology, 2004 Jun, 251 (6) 715-24

Otto M, Cepek L, Ratzka P, Doehlinger S, Boekhoff I, Wiltfang J, Irle E, Pergande G, Ellers-Lenz B, Windl O, Kretzschmar HA, Poser S & Prange H
Efficacy of flupirtine on cognitive function in patients with CJD: A double-blind study.
Neurology, 2004 Mar 09, 62 (5) 714-8


Kretzschmar HA, Sethi S, Földvári Z, Windl O, Querner V, Zerr I & Poser S
Latrogenic Creutzfeldt-Jakob disease with florid plaques.
Brain pathology (Zurich, Switzerland), 2003 Jul, 13 (3) 245-9


Tschampa HJ, Herms JW, Schulz-Schaeffer WJ, Maruschak B, Windl O, Jastrow U, Zerr I, Steinhoff BJ, Poser S & Kretzschmar HA
Clinical findings in sporadic Creutzfeldt-Jakob disease correlate with thalamic pathology.
Brain : a journal of neurology, 2002 Nov, 125 (Pt 11) 2558-66

Wegner C, Römer A, Schmalzbauer R, Lorenz H, Windl O & Kretzschmar HA
Mutant prion protein acquires resistance to protease in mouse neuroblastoma cells.
The Journal of general virology, 2002 May, 83 (Pt 5) 1237-1245

Lorenz H, Windl O & Kretzschmar HA
Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases.
The Journal of biological chemistry, 2002 Mar 08, 277 (10) 8508-16

Tumani H, Windl O, Kretzschmar HA & Ludolph AC
[Clinically atypical CJD: diagnostic relevance of cerebrospinal fluid markers and molecular genetic analysis?].
Deutsche medizinische Wochenschrift (1946), 2002 Feb 15, 127 (7) 318-20


Kramer ML, Kratzin HD, Schmidt B, Römer A, Windl O, Liemann S, Hornemann S & Kretzschmar H
Prion protein binds copper within the physiological concentration range.
The Journal of biological chemistry, 2001 May 18, 276 (20) 16711-9

Oehmichen M, Schulz-Schaeffer W, Kretzschmar H, Theuerkauf I, Gerling I, Windl O & Meissner C
Creutzfeldt-Jakob disease (CJD) in a case of suspected chronic heavy metal poisoning.
Journal of forensic sciences, 2001 May, 46 (3) 702-7


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
Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variants.
Annals of neurology, 2000 Sep, 48 (3) 323-9

Otto M, Esselmann H, Schulz-Shaeffer W, Neumann M, Schröter A, Ratzka P, Cepek L, Zerr I, Steinacker P, Windl O, Kornhuber J, Kretzschmar HA, Poser S & Wiltfang J
Decreased beta-amyloid1-42 in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.
Neurology, 2000 Mar 14, 54 (5) 1099-102


Harder A, Jendroska K, Kreuz F, Wirth T, Schafranka C, Karnatz N, Théallier-Janko A, Dreier J, Lohan K, Emmerich D, Cervós-Navarro J, Windl O, Kretzschmar HA, Nürnberg P & Witkowski R
Novel twelve-generation kindred of fatal familial insomnia from germany representing the entire spectrum of disease expression.
American journal of medical genetics, 1999 Dec 03, 87 (4) 311-6

Skworc KH, Windl O, Schulz-Schaeffer WJ, Giese A, Bergk J, Nägele A, Vieregge P, Zerr I, Poser S & Kretzschmar HA
Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene.
Annals of neurology, 1999 Nov, 46 (5) 693-700

Skworc KH, Windl O, Schulz-Schaeffer WJ, Giese A, Bergk J, Nagele A, Vieregge P, Zerr I, Poser S & Kretzschmar HA
Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene.
Annals of neurology, 1999 Nov, 46 (5) 693-700

Herms J, Tings T, Gall S, Madlung A, Giese A, Siebert H, Schürmann P, Windl O, Brose N & Kretzschmar H
Evidence of presynaptic location and function of the prion protein.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 1999 Oct 15, 19 (20) 8866-75

Windl O, Giese A, Schulz-Schaeffer W, Zerr I, Skworc K, Arendt S, Oberdieck C, Bodemer M, Poser S & Kretzschmar HA
Molecular genetics of human prion diseases in Germany.
Human genetics, 1999 Sep, 105 (3) 244-52

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
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.
Annals of neurology, 1999 Aug, 46 (2) 224-33

Almer G, Hainfellner JA, Brücke T, Jellinger K, Kleinert R, Bayer G, Windl O, Kretzschmar HA, Hill A, Sidle K, Collinge J & Budka H
Fatal familial insomnia: a new Austrian family.
Brain : a journal of neurology, 1999 Jan, 122 ( Pt 1) 5-16

Windl O, Lorenz H, Behrens C, R Mer A & Kretzschmar HA
Construction and characterization of murine neuroblastoma cell clones allowing inducible and high expression of the prion protein.
The Journal of general virology, 1999 Jan, 80 ( Pt 1) 15-21

Kropp S, Schulz-Schaeffer WJ, Finkenstaedt M, Riedemann C, Windl O, Steinhoff BJ, Zerr I, Kretzschmar HA & Poser S
The Heidenhain variant of Creutzfeldt-Jakob disease.
Archives of neurology, 1999 Jan, 56 (1) 55-61


Zerr I, Giese A, Windl O, Kropp S, Schulz-Schaeffer W, Riedemann C, Skworc K, Bodemer M, Kretzschmar HA & Poser S
Phenotypic variability in fatal familial insomnia (D178N-129M) genotype.
Neurology, 1998 Nov, 51 (5) 1398-405

Kretzschmar H, Giese A, Zerr I, Windl O, Schulz-Schaeffer W, Skworc K & Poser S
The German FFI cases.
Brain pathology (Zurich, Switzerland), 1998 Jul, 8 (3) 559-61

Zerr I, Bodemer M, Gefeller O, Otto M, Poser S, Wiltfang J, Windl O, Kretzschmar HA & Weber T
Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease.
Annals of neurology, 1998 Jan, 43 (1) 32-40


Weis J, Kretzschmar HA, Windl O, Podoll K & Schwarz M
Fatal spongiform encephalopathy in a patient who had handled animal feed.
Lancet (London, England), 1996 Nov 02, 348 (9036) 1240

Zerr I, Bodemer M, Otto M, Poser S, Windl O, Kretzschmar HA, Gefeller O & Weber T
Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluid.
Lancet (London, England), 1996 Sep 28, 348 (9031) 846-9

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
Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.
Human genetics, 1996 Sep, 98 (3) 259-64

Schulz-Schaeffer WJ, Giese A, Windl O & Kretzschmar HA
Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease.
Clinical neuropathology, 1996, 15 (6) 353-7


Windl O, Dempster M, Estibeiro P & Lathe R
A candidate marsupial PrP gene reveals two domains conserved in mammalian PrP proteins.
Gene, 1995 Jul 04, 159 (2) 181-6

Nicholl D, Windl O, de Silva R, Sawcer S, Dempster M, Ironside JW, Estibeiro JP, Yuill GM, Lathe R & Will RG
Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.
Journal of neurology, neurosurgery, and psychiatry, 1995 Jan, 58 (1) 65-9


de Silva R, Ironside JW, McCardle L, Esmonde T, Bell J, Will R, Windl O, Dempster M, Estibeiro P & Lathe R
Neuropathological phenotype and 'prion protein' genotype correlation in sporadic Creutzfeldt-Jakob disease.
Neuroscience letters, 1994 Sep 26, 179 (1-2) 50-2


Davies PT, Jahfar S, Ferguson IT & Windl O
Creutzfeldt-Jakob disease in individual occupationally exposed to BSE.
Lancet (London, England), 1993 Sep 11, 342 (8872) 680