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O Bandmann

Showing results (21-30 of 45) with videos related to

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Advances in Neurology|July 20, 1999
Toxins, genetics, and Parkinson's disease: the role of N-acetyltransferase 2O Bandmann, J Vaughan, P A Holmans, et al.
Neurology|March 29, 2006
Lack of association with TorsinA haplotype in German patients with sporadic dystoniaS Hague, S Klaffke, J Clarimon, et al.
Experimental Neurology|April 15, 2004
Slow N-acetyltransferase 2 status leads to enhanced intrastriatal dopamine depletion in 6-hydroxydopamine-lesioned ratsM Grundmann, C D Earl, J Sautter, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 14, 1999
GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsivenessR Robinson, G T McCarthy, O Bandmann, et al.
Journal of Neurology|April 1, 1997
Mitochondrial DNA polymorphisms in pathologically proven Parkinson's diseaseO Bandmann, M G Sweeney, S E Daniel, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 17, 2002
Steele-Richardson-Olszewski-syndrome: the relation of dopamine D2 receptor binding and subcortical lesions in MRIG Arnold, J Schwarz, K Tatsch, et al.
Human Molecular Genetics|March 1, 1996
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneityO Bandmann, T G Nygaard, R Surtees, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1995
CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophyV Planté-Bordeneuve, O Bandmann, G Wenning, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1996
Signal changes on MRI and increases in reactive microgliosis, astrogliosis, and iron in the putamen of two patients with multiple system atrophyJ Schwarz, S Weis, E Kraft, et al.
European Journal of Neurology|May 20, 2008
Immunophenotyping in Tourette syndrome--a pilot studyJ C Möller, B Tackenberg, M Heinzel-Gutenbrunner, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Advances in Neurology|July 20, 1999
Toxins, genetics, and Parkinson's disease: the role of N-acetyltransferase 2O Bandmann, J Vaughan, P A Holmans, et al.
Neurology|March 29, 2006
Lack of association with TorsinA haplotype in German patients with sporadic dystoniaS Hague, S Klaffke, J Clarimon, et al.
Experimental Neurology|April 15, 2004
Slow N-acetyltransferase 2 status leads to enhanced intrastriatal dopamine depletion in 6-hydroxydopamine-lesioned ratsM Grundmann, C D Earl, J Sautter, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 14, 1999
GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsivenessR Robinson, G T McCarthy, O Bandmann, et al.
Journal of Neurology|April 1, 1997
Mitochondrial DNA polymorphisms in pathologically proven Parkinson's diseaseO Bandmann, M G Sweeney, S E Daniel, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 17, 2002
Steele-Richardson-Olszewski-syndrome: the relation of dopamine D2 receptor binding and subcortical lesions in MRIG Arnold, J Schwarz, K Tatsch, et al.
Human Molecular Genetics|March 1, 1996
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneityO Bandmann, T G Nygaard, R Surtees, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1995
CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophyV Planté-Bordeneuve, O Bandmann, G Wenning, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1996
Signal changes on MRI and increases in reactive microgliosis, astrogliosis, and iron in the putamen of two patients with multiple system atrophyJ Schwarz, S Weis, E Kraft, et al.
European Journal of Neurology|May 20, 2008
Immunophenotyping in Tourette syndrome--a pilot studyJ C Möller, B Tackenberg, M Heinzel-Gutenbrunner, et al.
Pageof 5