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List of works by Oliver Bandmann

3H-spiperone binding to lymphocytes fails in the differential diagnosis of de novo Parkinson syndromes

scientific article published on January 1993

A contrast enhanced lesion of the III nerve on MR of a patient with ophthalmoplegic migraine as evidence for a Tolosa-Hunt syndrome

scientific article published on 01 September 1993

A genetic study of Wilson's disease in the United Kingdom

scientific article published on 21 March 2013

Animal models of Wilson disease

scientific article published on 26 June 2018

Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's disease

scientific article published in December 1994

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

scientific article published on November 1995

Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease

scientific article published in October 1997

Biomarkers for PD: How can we approach complexity?

scientific article

Brain-derived neurotrophic factor: a genetic risk factor for obsessive-compulsive disorder and Tourette syndrome?

scientific article published in June 2006

C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study.

scientific article published on 24 July 2013

CNS involvement in hereditary neuropathy with pressure palsies (HNPP).

scientific article

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.

scientific article published on May 1995

Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio).

scientific article

Complicated autosomal recessive hereditary spastic paraplegia: a complex picture is emerging

scientific article published on 01 April 2008

Corpus callosum morphology and microstructure assessed using structural MR imaging and diffusion tensor imaging: initial findings in adults with neurofibromatosis type 1.

scientific article published on 18 March 2010

Delayed toxic-hypoxic encephalopathy

scientific article published in April 2013

Dopa-responsive dystonia -- the story so far.

scientific article

Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity

scientific article published on 01 March 1996

Dopa-responsive dystonia: A clinical and molecular genetic study

scientific article published on 01 October 1998

Dopamine receptor gene polymorphisms in Parkinson's disease patients reporting "sleep attacks".

scientific article published in November 2004

Epidemiology and introduction to the clinical presentation of Wilson disease.

scientific article published on January 2017

Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome

scientific article

Evaluation of the Unified Wilson's Disease Rating Scale (UWDRS) in German patients with treated Wilson's disease

scientific article published in January 2008

Genetic zebrafish models of neurodegenerative diseases.

scientific article published on 20 May 2010

Genetics of multiple system atrophy: Back to square one?

scientific article published on 14 September 2016

Glucocerebrosidase 1 deficient Danio rerio mirror key pathological aspects of human Gaucher disease and provide evidence of early microglial activation preceding alpha-synuclein-independent neuronal cell death

scientific article

Heterozygous mutations in the FGF8, SHH and nodal/transforming growth factor beta pathways do not confer increased dopaminergic neuron vulnerability--a zebrafish study

scientific article published on 2 November 2012

Huntington disease: More common than you think?

scientific article published on 22 June 2016

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

scientific article published on 19 June 2017

Immunophenotyping in Tourette syndrome--a pilot study

scientific article published on 15 May 2008

Inhibition of the mitochondrial calcium uniporter rescues dopaminergic neurons in pink1-/- zebrafish

scientific article

Lack of association between the interleukin-1 alpha (-889) polymorphism and early-onset Parkinson's disease

scientific article published in April 2004

Lack of association with TorsinA haplotype in German patients with sporadic dystonia

scientific article published on 01 March 2006

Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease

scientific article published on April 1997

Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2.

scientific article published on November 2010

Neurological letter from Bangladesh

scientific article published on 28 August 2020

Neuronal dark matter: the emerging role of microRNAs in neurodegeneration

scientific article

Normal dopaminergic and serotonergic metabolites in cerebrospinal fluid and blood of restless legs syndrome patients

scientific article published in February 2004

Parkinson disease, cancer, and LRRK2: causation or association?

scientific article published on 8 February 2012

Porphyria: often discussed but too often missed

scientific article published on 14 March 2018

Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's disease

scientific article published on 01 October 2006

Rapamycin activation of 4E-BP prevents parkinsonian dopaminergic neuron loss.

scientific article published on 16 August 2009

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

scientific article published on 10 July 2016

Slow N-acetyltransferase 2 status leads to enhanced intrastriatal dopamine depletion in 6-hydroxydopamine-lesioned rats

scientific article published in May 2004

Steele-Richardson-Olszewski-syndrome: the relation of dopamine D2 receptor binding and subcortical lesions in MRI.

scientific article published in April 2002

Structural and Functional Neuroimaging of Visual Hallucinations in Lewy Body Disease: A Systematic Literature Review

scientific article

The GTP-cyclohydrolase I gene in atypical parkinsonian patients: a clinico-genetic study

scientific article published on September 1996

The Prevalence of Juvenile Huntington's Disease: A Review of the Literature and Meta-Analysis.

scientific article

The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease

scientific article

The common PARK8 mutation LRRK2G²⁰¹⁹S is not a risk factor for breast cancer in the absence of Parkinson's disease

scientific article published on 4 July 2013

The documentation of consent and disclosure of neurogenetic testing outside clinical genetics.

scientific article published on 11 February 2014

The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group

scientific article

The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease

scientific article published on June 1996

The influence of the zebrafish genetic background on Parkinson's disease-related aspects

scientific article published on 11 July 2011

TigarB causes mitochondrial dysfunction and neuronal loss in PINK1 deficiency

scientific article published on December 2013

Transglutaminase 6 antibodies in the diagnosis of gluten ataxia

scientific article

Translational approaches to restoring mitochondrial function in Parkinson's disease.

scientific article published on 27 November 2017

UDCA exerts beneficial effect on mitochondrial dysfunction in LRRK2(G2019S) carriers and in vivo.

scientific article

Ursocholanic acid rescues mitochondrial function in common forms of familial Parkinson's disease

scientific article

Ursodeoxycholic acid as a novel disease-modifying treatment for Parkinson's disease: protocol for a two-centre, randomised, double-blind, placebo-controlled trial, The 'UP' study

scientific article published on 05 August 2020

Wilson's disease and other neurological copper disorders

scientific article

Yet another spinocerebellar ataxia: the saga continues

scientific article published in August 2008

Zebrafish as a new animal model for movement disorders

scientific article published on 04 May 2008

p53-dependent neuronal cell death in a DJ-1-deficient zebrafish model of Parkinson's disease

scientific article published on 12 December 2006

pH-sensitive tubular polymersomes: formation and applications in cellular delivery.

scientific article published on 29 April 2014

β-Defensin Genomic Copy Number Does Not Influence the Age of Onset in Huntington's Disease

scientific article published on March 2013

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