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European Neurology|August 31, 2001
Nail-patella syndrome associated with respiratory chain disorderJ Finsterer, C Stöllberger, J Wanschitz, et al.
Acta Neuropathologica|March 29, 2001
Autoradiography with [3H]PK11195 of spinal tract degeneration in amyotrophic lateral sclerosisH H Sitte, J Wanschitz, H Budka, et al.
The American Journal of Pathology|November 7, 1999
Selective neuronal vulnerability in human prion diseases. Fatal familial insomnia differs from other types of prion diseasesM Guentchev, J Wanschitz, T Voigtländer, et al.
Acta Neurologica Scandinavica|February 27, 2016
Secondary myopathy due to systemic diseasesJ Finsterer, W N Löscher, J Wanschitz, et al.
Neurology|October 27, 1997
Ganglionitis in paraneoplastic subacute sensory neuronopathy: a morphologic studyJ Wanschitz, J A Hainfellner, W Kristoferitsch, et al.
Acta Neuropathologica|January 1, 1995
Suprasellar meningioma with expression of glial fibrillary acidic protein: a peculiar variantJ Wanschitz, M Schmidbauer, H Maier, et al.
Neuropathology and Applied Neurobiology|February 14, 1998
Proliferation and DNA fragmentation in meningioma subtypesH Maier, J Wanschitz, R Sedivy, et al.
Acta Neurologica Scandinavica|March 16, 2017
Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's diseaseJ Finsterer, J Wanschitz, S Quasthoff, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositisO Dubourg, J Wanschitz, T Maisonobe, et al.
Neurology|January 10, 2001
Hypertrophic chronic pachymeningitis as a localized immune process in the craniocervical regionB Voller, K Vass, J Wanschitz, et al.
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