Neurodegenerative disorders: Parkinson's disease and Huntington's disease

Por Hague, S, Klaffke, S, Bandmann, O
Publicado em 2005

Debrisoquine hydroxylase polymorphism in Leber's hereditary optic neuropathy.

Por Chalmers, R M, Bandmann, O, Harding, A E
Publicado em 1996

GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugs

Por Jarman, P., Bandmann, O, Marsden, C, Wood, N
Publicado em 1997

Rescue of mitochondrial function in parkin-mutant fibroblasts using drug loaded PMPC-PDPA polymersomes and tubular polymersomes

Por Yealland, G., Battaglia, G., Bandmann, O., Mortiboys, H
Publicado no Neurosci Lett (2016)

Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's disease.

Por Bandmann, O, Davis, M B, Marsden, C D, Harding, A E
Publicado em 1995

Arg296 to Cys296 polymorphism in exon 6 of cytochrome P-450-2D6 (CYP2D6) is not associated with multiple system atrophy.

Por Bandmann, O, Wenning, G K, Quinn, N P, Harding, A E
Publicado em 1995

GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsiveness

Por Robinson, R., McCarthy, G., Bandmann, O., Dobbie, M., Surtees, R., Wood, N.
Publicado em 1999

The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases

Por Morris, H, Janssen, J, Bandmann, O, Daniel, S, Rossor, M, Lees, A, Wood, N
Publicado em 1999

Signal changes on MRI and increases in reactive microgliosis, astrogliosis, and iron in the putamen of two patients with multiple system atrophy.

Por Schwarz, J, Weis, S, Kraft, E, Tatsch, K, Bandmann, O, Mehraein, P, Vogl, T, Oertel, W H
Publicado em 1996