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Neurosurgery|January 11, 2001
Genotype-phenotype correlation in gemistocytic astrocytomasS Kösel, B W Scheithauer, M B GraeberBrain Pathology (Zurich, Switzerland)|October 1, 1993
Non-radioactive direct sequencing of PCR products amplified from neuropathological specimensS Kösel, M B GraeberActa Neuropathologica|January 1, 1994
Use of neuropathological tissue for molecular genetic studies: parameters affecting DNA extraction and polymerase chain reactionS Kösel, M B GraeberBiochemical and Biophysical Research Communications|September 15, 1994
No association of mutations at nucleotide 5460 of mitochondrial NADH dehydrogenase with Alzheimer's diseaseS Kösel, R Egensperger, P Mehraein, et al.Biochemical and Biophysical Research Communications|June 15, 1995
Absence of the mitochondrial A7237T mutation in Parkinson's diseaseC B Lücking, S Kösel, P Mehraein, et al.Clinical Neuropathology|November 1, 1996
Regional heterogeneity of mtDNA heteroplasmy in parkinsonian brainN M Schnopp, S Kösel, R Egensperger, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 26, 1997
The 'common deletion' is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reactionS Kösel, R Egensperger, N M Schnopp, et al.Brain Pathology (Zurich, Switzerland)|July 21, 1998
Microglial activation in Alzheimer disease: Association with APOE genotypeR Egensperger, S Kösel, U von Eitzen, et al.Journal of Neuroscience Research|April 29, 1998
Neurodegeneration and aging: role of the second genomeM B Graeber, E Grasbon-Frodl, U V Eitzen, et al.Parkinsonism & Related Disorders|July 2, 2008
Nigral neurons are likely to die of a mechanism other than classical apoptosis in Parkinson's diseaseM B Graeber, E Grasbon-Frodl, P Abell-Aleff, et al.Pageof 53