Research Topics
Genomes and Genes | O BandmannSummaryAffiliation: University of Sheffield Country: UK Publications
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Detail Information
Publications
Genetic zebrafish models of neurodegenerative diseasesOliver Bandmann
Academic Neurology Unit, Department of Neuroscience, University of Sheffield, UK
Neurobiol Dis 40:58-65. 2010....- 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.... - Neurodegenerative disorders: Parkinson's disease and Huntington's diseaseS M Hague
Academic Neurology Unit, Division of Genomic Medicine, University of Sheffield, UK
J Neurol Neurosurg Psychiatry 76:1058-63. 2005.... - Copper genes are not implicated in the pathogenesis of focal dystoniaO Bandmann
Department of Neurology, Philipps-University Marburg, Germany
Neurology 59:782-3. 2002 - The phenylalanine loading test in the differential diagnosis of dystoniaO 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... - Lack of association with TorsinA haplotype in German patients with sporadic dystoniaS Hague
Division of Genomic Medicine, University of Sheffield, UK
Neurology 66:951-2. 2006 - Candidate gene studies in focal dystoniaD 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... - Slow N-acetyltransferase 2 status leads to enhanced intrastriatal dopamine depletion in 6-hydroxydopamine-lesioned ratsM 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... - Immunophenotyping in Tourette syndrome--a pilot studyJ 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... - Different postural reaction patterns for expected and unexpected perturbations in patients with idiopathic Parkinson's disease and other parkinsonian syndromesI 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... - 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... - Dopa-responsive dystonia -- the story so farO 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... - Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2Heather 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... - Yet another spinocerebellar ataxia: the saga continuesO Bandmann
Neurology 71:542-3. 2008 - The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study GroupC Kamm
Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, Hoppe-Seyler-Strasse 3, , , 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... - Dopa-responsive dystonia: a clinical and molecular genetic studyO 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... - Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneityO 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... - The human homologue of the weaver mouse gene in familial and sporadic Parkinson's diseaseO 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...