O Bandmann

Summary

Affiliation: University of Sheffield
Country: UK

Publications

  1. pmc A genetic study of Wilson's disease in the United Kingdom
    Alison J Coffey
    Department of Neuroscience, The University of Sheffield, 385a Glossop Road, Sheffield S10 2HQ, UK
    Brain 136:1476-87. 2013
  2. doi request reprint Genetic zebrafish models of neurodegenerative diseases
    Oliver Bandmann
    Academic Neurology Unit, Department of Neuroscience, University of Sheffield, UK
    Neurobiol Dis 40:58-65. 2010
  3. pmc Neurodegenerative disorders: Parkinson's disease and Huntington's disease
    S M Hague
    Academic Neurology Unit, Division of Genomic Medicine, University of Sheffield, UK
    J Neurol Neurosurg Psychiatry 76:1058-63. 2005
  4. doi request reprint Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio)
    Laura Flinn
    Academic Neurology Unit, Medical School, University of Sheffield, Beech Hill Road, Sheffield, UK
    Brain 132:1613-23. 2009
  5. ncbi request reprint Copper genes are not implicated in the pathogenesis of focal dystonia
    O Bandmann
    Department of Neurology, Philipps University Marburg, Germany
    Neurology 59:782-3. 2002
  6. ncbi request reprint The phenylalanine loading test in the differential diagnosis of dystonia
    O Bandmann
    Department of Neurology, Philipps University Marburg, Germany
    Neurology 60:700-2. 2003
  7. ncbi request reprint Lack of association with TorsinA haplotype in German patients with sporadic dystonia
    S Hague
    Division of Genomic Medicine, University of Sheffield, UK
    Neurology 66:951-2. 2006
  8. ncbi request reprint Candidate gene studies in focal dystonia
    D Sibbing
    Department of Neurology, Philipps University, Marburg, Germany
    Neurology 61:1097-101. 2003
  9. doi request reprint Immunophenotyping in Tourette syndrome--a pilot study
    J C Moller
    Department of Neurology, Philipps University, Marburg, Germany
    Eur J Neurol 15:749-53. 2008
  10. ncbi request reprint Slow N-acetyltransferase 2 status leads to enhanced intrastriatal dopamine depletion in 6-hydroxydopamine-lesioned rats
    M Grundmann
    Department of Neurology, Philipps University, Marburg, Germany
    Exp Neurol 187:199-202. 2004

Collaborators

Detail Information

Publications19

  1. pmc A genetic study of Wilson's disease in the United Kingdom
    Alison J Coffey
    Department of Neuroscience, The University of Sheffield, 385a Glossop Road, Sheffield S10 2HQ, UK
    Brain 136:1476-87. 2013
    ....
  2. doi request reprint Genetic zebrafish models of neurodegenerative diseases
    Oliver Bandmann
    Academic Neurology Unit, Department of Neuroscience, University of Sheffield, UK
    Neurobiol Dis 40:58-65. 2010
    ....
  3. pmc Neurodegenerative disorders: Parkinson's disease and Huntington's disease
    S M Hague
    Academic Neurology Unit, Division of Genomic Medicine, University of Sheffield, UK
    J Neurol Neurosurg Psychiatry 76:1058-63. 2005
    ....
  4. doi request reprint Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio)
    Laura Flinn
    Academic Neurology Unit, Medical School, University of Sheffield, Beech Hill Road, Sheffield, UK
    Brain 132:1613-23. 2009
    ....
  5. ncbi request reprint Copper genes are not implicated in the pathogenesis of focal dystonia
    O Bandmann
    Department of Neurology, Philipps University Marburg, Germany
    Neurology 59:782-3. 2002
  6. ncbi request reprint The phenylalanine loading test in the differential diagnosis of dystonia
    O Bandmann
    Department of Neurology, Philipps University Marburg, Germany
    Neurology 60:700-2. 2003
    ..A marked difference in the phenylalanine/tyrosine ratio between patients with DRD and patients with other types of dystonia was observed. This indicates that Phe-L may be helpful in the differential diagnosis of dystonias...
  7. ncbi request reprint Lack of association with TorsinA haplotype in German patients with sporadic dystonia
    S Hague
    Division of Genomic Medicine, University of Sheffield, UK
    Neurology 66:951-2. 2006
  8. ncbi request reprint Candidate gene studies in focal dystonia
    D Sibbing
    Department of Neurology, Philipps University, Marburg, Germany
    Neurology 61:1097-101. 2003
    ..Mutations in the DYT1 gene can cause focal dystonia, and an association with a polymorphism in the D5 receptor gene (DRD5) has been reported but not confirmed...
  9. doi request reprint Immunophenotyping in Tourette syndrome--a pilot study
    J C Moller
    Department of Neurology, Philipps University, Marburg, Germany
    Eur J Neurol 15:749-53. 2008
    ..The cause of Tourette syndrome (TS) is not precisely known, although several lines of evidence point at an involvement of the immune system in its pathogenesis...
  10. ncbi request reprint Slow N-acetyltransferase 2 status leads to enhanced intrastriatal dopamine depletion in 6-hydroxydopamine-lesioned rats
    M Grundmann
    Department of Neurology, Philipps University, Marburg, Germany
    Exp Neurol 187:199-202. 2004
    ..Nigral dopaminergic cell counts were also lower in the WKY rats, but this difference failed to reach statistical significance, suggesting that slow acetylation is especially deleterious at the level of striatal nerve endings...
  11. ncbi request reprint Different postural reaction patterns for expected and unexpected perturbations in patients with idiopathic Parkinson's disease and other parkinsonian syndromes
    I Immisch
    Department of Neurology, Klinikum Grosshadern, Ludwig Maximilians University, Munich, Germany
    Eur J Neurol 6:549-54. 1999
    ..These differences in postural stability could serve as an additional tool for differential diagnosis...
  12. ncbi request reprint CNS involvement in hereditary neuropathy with pressure palsies (HNPP)
    B Tackenberg
    Department of Neurology, Philipps University, Marburg, Germany
    Neurology 67:2250-2. 2006
    ..MRI abnormalities were observed in four patients. Our study suggests subclinical but functionally relevant CNS myelin damage in HNPP...
  13. ncbi request reprint Dopa-responsive dystonia -- the story so far
    O Bandmann
    Department of Neurology, Philipps University, Marburg, Germany
    Neuropediatrics 33:1-5. 2002
    ..Particular emphasis is given to clinically relevant aspects such as diagnostic difficulties and atypical presentations in infancy and early childhood...
  14. doi request reprint Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2
    Heather Mortiboys
    Academic Neurology Unit, Medical School, University of Sheffield, Beech Hill Road, Sheffield S10 2RX, UK
    Neurology 75:2017-20. 2010
    ..The aim of our study was to assess mitochondrial function and morphology in LRRK2(G2019S) mutant patient tissue to determine whether impaired mitochondrial function and morphology are shared features in early-onset and late-onset PD...
  15. doi request reprint Yet another spinocerebellar ataxia: the saga continues
    O Bandmann
    Neurology 71:542-3. 2008
  16. ncbi request reprint The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group
    C Kamm
    Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, Hoppe Seyler Strasse 3, University of Tubingen, 72086 Tübingen, Germany
    Brain 128:1855-60. 2005
    ..On the basis of our data, the EMSA Study Group does not recommend routine FMR1 genotyping in typical MSA patients...
  17. ncbi request reprint Dopa-responsive dystonia: a clinical and molecular genetic study
    O Bandmann
    Institute of Neurology, London, UK
    Ann Neurol 44:649-56. 1998
    ..None of our DRD patients without a mutation in GCH-1 had the 3-bp deletion recently detected in DYT1, the causative gene for idiopathic torsion dystonia with linkage to 9q34...
  18. ncbi request reprint Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity
    O Bandmann
    University Department of Clinical Neurology, Institute of Neurology, London, UK
    Hum Mol Genet 5:403-6. 1996
    ..None of these mutations were detected more than once and none of the mutations previously described were found in our patients. No mutations were identified in four families and in two sporadic cases...
  19. ncbi request reprint The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease
    O Bandmann
    University Department of Clinical Neurology Neurogenetics and Movement Disorders Section, Institute of Neurology, London, U K
    Neuroscience 72:877-9. 1996
    ..The sequence was normal in all cases examined, suggesting a differing aetiology of nigral cell loss in Parkinson's disease and weaver mice...