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European Neurology|June 1, 2000
Nerve conduction studies in multiple system atrophyM Abele, J B Schulz, K Bürk, et al.Journal of Neurology|August 1, 1995
Fixation instability and oculomotor abnormalities in Friedreich's ataxiaS Spieker, J B Schulz, D Petersen, et al.Molecular and Cellular Biochemistry|October 6, 1997
The role of mitochondrial dysfunction and neuronal nitric oxide in animal models of neurodegenerative diseasesJ B Schulz, R T Matthews, T Klockgether, et al.Acta Neurologica Scandinavica|February 24, 2000
Evoked potentials in multiple system atrophy (MSA)M Abele, J B Schulz, K Bürk, et al.Journal of Neurology|February 1, 1994
Oculomotor abnormalities and MRI findings in idiopathic cerebellar ataxiaM Fetter, T Klockgether, J B Schulz, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1994
Visual control of arm movement in Parkinson's diseaseT Klockgether, J DichgansJournal of Neural Transmission. Supplementum|January 1, 1997
Developmental and genetic regulation of programmed neuronal deathM Weller, J B Schulz, U Wüllner, et al.Neurology|May 29, 2001
Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletionsC Kornblum, R Broicher, E Walther, et al.Brain Research|March 25, 1996
Acceleration deficit in patients with cerebellar lesions. A study of kinematic and EMG-parameters in fast wrist movementsB Wild, T Klockgether, J DichgansDer Nervenarzt|July 21, 1999
[New insights in the molecular genetics and pathophysiology of hereditary ataxias]K Bürk, T Klockgether, J DichgansPageof 77