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Journal of Neurology, Neurosurgery, and Psychiatry|November 5, 1997
GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugsP R Jarman, O Bandmann, C D Marsden, et al.Neuroscience|June 1, 1996
The human homologue of the weaver mouse gene in familial and sporadic Parkinson's diseaseO Bandmann, M B Davis, C D Marsden, et al.Lancet (London, England)|October 31, 1997
Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's diseaseO Bandmann, J Vaughan, P Holmans, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 14, 2000
Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's diseaseO Bandmann, J R Vaughan, P Holmans, et al.Journal of the Neurological Sciences|September 15, 1996
The GTP-cyclohydrolase I gene in atypical parkinsonian patients: a clinico-genetic studyO Bandmann, S Daniel, C D Marsden, 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.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.Neurology|December 31, 1997
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degenerationO Bandmann, M G Sweeney, S E Daniel, et al.Pageof 17