Lista de obras - Oliver Bandmann - Dominio Público Uruguay

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

artículo científico publicado en 1993

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

artículo científico publicado en 1993

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

artículo científico publicado en 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

artículo científico publicado en 1994

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

artículo científico publicado en 1995

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

artículo científico publicado en 1997

Biomarkers for PD: How can we approach complexity?

artículo científico publicado en 2013

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

artículo científico publicado en 2006

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

artículo científico publicado en 2013

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

artículo científico publicado en 2006

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.

artículo científico publicado en 1995

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

artículo científico publicado en 2009

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.

artículo científico publicado en 2010

Delayed toxic-hypoxic encephalopathy

artículo científico publicado en 2013

Dopa-responsive dystonia -- the story so far.

artículo científico publicado en 2002

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

artículo científico publicado en 1996

Dopa-responsive dystonia: A clinical and molecular genetic study

artículo científico publicado en 1998

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

artículo científico publicado en 2004

Epidemiology and introduction to the clinical presentation of Wilson disease.

artículo científico publicado en 2017

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

artículo científico publicado en 2005

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

artículo científico publicado en 2008

Genetic zebrafish models of neurodegenerative diseases.

artículo científico publicado en 2010

Genetics of multiple system atrophy: Back to square one?

artículo científico publicado en 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

artículo científico publicado en 2015

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

artículo científico publicado en 2012

Huntington disease: More common than you think?

artículo científico publicado en 2016

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

artículo científico

Immunophenotyping in Tourette syndrome--a pilot study

artículo científico publicado en 2008

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

artículo científico publicado en 2016

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

artículo científico publicado en 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

artículo científico publicado en 1997

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

artículo científico publicado en 2010

Neurological letter from Bangladesh

artículo científico publicado en 2020

Neuronal dark matter: the emerging role of microRNAs in neurodegeneration

artículo científico publicado en 2013

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

artículo científico publicado en 2004

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

artículo científico publicado en 2012

Porphyria: often discussed but too often missed

artículo científico publicado en 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.

artículo científico publicado en 2009

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

artículo científico publicado en 2016

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

artículo científico publicado en 2004

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

artículo científico publicado en 2002

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

artículo científico publicado en 2017

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

artículo científico publicado en 1996

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

artículo científico publicado en 2012

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

artículo científico publicado en 1998

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

artículo científico publicado en 2013

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

artículo científico

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

artículo científico publicado en 2005

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

artículo científico publicado en 1996

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

artículo científico publicado en 2011

TigarB causes mitochondrial dysfunction and neuronal loss in PINK1 deficiency

artículo científico publicado en 2013

Transglutaminase 6 antibodies in the diagnosis of gluten ataxia

artículo científico publicado en 2013

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

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

artículo científico publicado en 2015

Yet another spinocerebellar ataxia: the saga continues

artículo científico publicado en 2008

Zebrafish as a new animal model for movement disorders

artículo científico publicado en 2008

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

artículo científico publicado en 2006

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

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Lista de obras de Oliver Bandmann

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

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

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

Animal models of Wilson disease

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

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

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

Biomarkers for PD: How can we approach complexity?

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

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

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

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.

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

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

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

Delayed toxic-hypoxic encephalopathy

Dopa-responsive dystonia -- the story so far.

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

Dopa-responsive dystonia: A clinical and molecular genetic study

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

Epidemiology and introduction to the clinical presentation of Wilson disease.

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

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

Genetic zebrafish models of neurodegenerative diseases.

Genetics of multiple system atrophy: Back to square one?

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

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

Huntington disease: More common than you think?

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

Immunophenotyping in Tourette syndrome--a pilot study

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

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

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

Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease

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

Neurological letter from Bangladesh

Neuronal dark matter: the emerging role of microRNAs in neurodegeneration

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

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

Porphyria: often discussed but too often missed

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

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

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

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

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

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

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

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

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

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

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

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

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

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

TigarB causes mitochondrial dysfunction and neuronal loss in PINK1 deficiency

Transglutaminase 6 antibodies in the diagnosis of gluten ataxia

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

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

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

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

Wilson's disease and other neurological copper disorders

Yet another spinocerebellar ataxia: the saga continues

Zebrafish as a new animal model for movement disorders

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

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

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