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Oliver Bandmann

Showing results (41-50 of 88) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 23, 2003
HLA-DRB genotyping in Gilles de la Tourette patients and their parentsSarah Schoenian, Inke Konig, Wolfgang Oertel, et al.
Nature Neuroscience|August 18, 2009
Rapamycin activation of 4E-BP prevents parkinsonian dopaminergic neuron lossLuke S Tain, Heather Mortiboys, Ran N Tao, et al.
Nuclear Medicine Communications|January 19, 2018
The subresolution DaTSCAN phantom: a cost-effective, flexible alternative to traditional phantom technologyJonathan C Taylor, Nicholas Vennart, Ian Negus, et al.
Annals of Neurology|January 31, 2003
The promoter region of the Menkes gene ATP7A is not altered in focal or generalized dystoniaDirk Sibbing, Iris Trender-Gerhardt, Nick W Wood, et al.
Neurology. Clinical Practice|March 20, 2020
Serum FGF-21, GDF-15, and blood mtDNA copy number are not biomarkers of Parkinson diseaseRyan L Davis, Siew L Wong, Phillippa J Carling, et al.
Neurologia I Neurochirurgia Polska|March 3, 2007
Unified Wilson's Disease Rating Scale - a proposal for the neurological scoring of Wilson's disease patientsAnna Członkowska, Beata Tarnacka, Jens Carsten Möller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2006
Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's diseaseJens Carsten Möller, Barbara Leinweber, Ida Rissling, et al.
ACS Nano|April 15, 2014
pH-sensitive tubular polymersomes: formation and applications in cellular deliveryJames D Robertson, Guy Yealland, Milagros Avila-Olias, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 24, 2004
Normal dopaminergic and serotonergic metabolites in cerebrospinal fluid and blood of restless legs syndrome patientsKarin Stiasny-Kolster, J Carsten Möller, Johannes Zschocke, et al.
Scientific Reports|June 25, 2026
Variable mitochondrial phenotypes and reduced complex IV assembly factor SCO2 in LRRK2-G2019S fibroblastsRuby Wallis, Ella Simmonite, Harry Cooper, et al.
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 23, 2003
HLA-DRB genotyping in Gilles de la Tourette patients and their parentsSarah Schoenian, Inke Konig, Wolfgang Oertel, et al.
Nature Neuroscience|August 18, 2009
Rapamycin activation of 4E-BP prevents parkinsonian dopaminergic neuron lossLuke S Tain, Heather Mortiboys, Ran N Tao, et al.
Nuclear Medicine Communications|January 19, 2018
The subresolution DaTSCAN phantom: a cost-effective, flexible alternative to traditional phantom technologyJonathan C Taylor, Nicholas Vennart, Ian Negus, et al.
Annals of Neurology|January 31, 2003
The promoter region of the Menkes gene ATP7A is not altered in focal or generalized dystoniaDirk Sibbing, Iris Trender-Gerhardt, Nick W Wood, et al.
Neurology. Clinical Practice|March 20, 2020
Serum FGF-21, GDF-15, and blood mtDNA copy number are not biomarkers of Parkinson diseaseRyan L Davis, Siew L Wong, Phillippa J Carling, et al.
Neurologia I Neurochirurgia Polska|March 3, 2007
Unified Wilson's Disease Rating Scale - a proposal for the neurological scoring of Wilson's disease patientsAnna Członkowska, Beata Tarnacka, Jens Carsten Möller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2006
Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's diseaseJens Carsten Möller, Barbara Leinweber, Ida Rissling, et al.
ACS Nano|April 15, 2014
pH-sensitive tubular polymersomes: formation and applications in cellular deliveryJames D Robertson, Guy Yealland, Milagros Avila-Olias, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 24, 2004
Normal dopaminergic and serotonergic metabolites in cerebrospinal fluid and blood of restless legs syndrome patientsKarin Stiasny-Kolster, J Carsten Möller, Johannes Zschocke, et al.
Scientific Reports|June 25, 2026
Variable mitochondrial phenotypes and reduced complex IV assembly factor SCO2 in LRRK2-G2019S fibroblastsRuby Wallis, Ella Simmonite, Harry Cooper, et al.
Pageof 9