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Novel twelve-generation kindred of fatal familial insomnia from germany representing the entire spectrum of disease expression.
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. Harder A, et al. Among authors: windl o. Am J Med Genet. 1999 Dec 3;87(4):311-6. doi: 10.1002/(sici)1096-8628(19991203)87:4<311::aid-ajmg6>3.0.co;2-5. Am J Med Genet. 1999. PMID: 10588836
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. Hum Genet. 1999 Sep;105(3):244-52. doi: 10.1007/s004399900124. Hum Genet. 1999. PMID: 10987652
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.
81 results