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Acta Neuropathologica|August 15, 1998
Coexistence of Alzheimer-type neuropathology in Creutzfeldt-Jakob diseaseJ A Hainfellner, J Wanschitz, K Jellinger, et al.Wiener Medizinische Wochenschrift (1946)|June 5, 1998
[Epidemiology of transmissible spongiform encephalopathies (prion diseases) in Austria]C Radbauer, J A Hainfellner, K Jellinger, et al.Acta Neuropathologica|December 14, 1999
Disease associated prion protein may deposit in the peripheral nervous system in human transmissible spongiform encephalopathiesJ A Hainfellner, H BudkaJournal of Neurology, Neurosurgery, and Psychiatry|August 1, 1996
Creutzfeldt-Jakob disease in AustriaJ A Hainfellner, K Jellinger, H Diringer, et al.Wiener Klinische Wochenschrift|December 13, 1996
[Creutzfeldt-Jakob disease in Austria]J A Hainfellner, K Jellinger, H Diringer, et al.Wiener Medizinische Wochenschrift (1946)|January 1, 1996
[Sporadic juvenile amyotrophic lateral sclerosis with neuronal basophil inclusion bodies--a nosologic entity?]M Schmidbauer, J A Hainfellner, H BudkaAnnals of Neurology|September 8, 2000
No tissue damage by chronic deep brain stimulation in Parkinson's diseaseC Haberler, F Alesch, P R Mazal, et al.Clinical Neuropathology|March 1, 1994
Neocortical changes in Parkinson's disease, revisitedH Sugiyama, J A Hainfellner, M Yoshimura, et al.Histopathology|January 30, 2007
OLIG2 is a useful immunohistochemical marker in differential diagnosis of clear cell primary CNS neoplasmsM Preusser, H Budka, K Rössler, et al.Acta Neuropathologica. Supplementum|January 1, 1975
SSPE-like inclusion body disorder in treated childhood leukemiaE Sluga, H Budka, K Jellinger, et al.Pageof 46