Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Andrew Singleton

Showing results (31-40 of 286) with videos related to

Pageof 29
Sort By:
Human Molecular Genetics|May 6, 2014
Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associationsRita Guerreiro, José Brás, John Hardy, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|February 18, 2015
Multiple system atrophy: the application of genetics in understanding etiologyMonica Federoff, Lucia V Schottlaender, Henry Houlden, et al.
Medical Education|October 1, 2008
Learning not to take it seriously: junior doctors' accounts of errorLeanda Kroll, Andrew Singleton, Joe Collier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 3, 2011
Parkinson's disease and α-synuclein expressionMichael J Devine, Katrina Gwinn, Andrew Singleton, et al.
The FEBS Journal|November 22, 2008
Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body diseaseJose Bras, Andrew Singleton, Mark R Cookson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 31, 2012
DYT16: the original casesSarah Camargos, Andrew J Lees, Andrew Singleton, et al.
Human Mutation|December 19, 2009
A thorough assessment of benign genetic variability in GRN and MAPTRita J Guerreiro, Nicole Washecka, John Hardy, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 16, 2005
Prion genotypes in Central America suggest selection for the V129 alleleJohn Hardy, Sonja Scholz, Whitney Evans, et al.
Neuroscience Letters|August 28, 2004
Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish populationJordi Clarimon, Johanna Eerola, Olli Hellström, et al.
Alzheimer Disease and Associated Disorders|July 3, 2009
A case of dementia with PRNP D178Ncis-129M and no insomniaRita J Guerreiro, Tina Vaskov, Cynthia Crews, et al.
Pageof 29

Showing results (31-40 of 286) with videos related to

Sort By:
Pageof 29
Human Molecular Genetics|May 6, 2014
Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associationsRita Guerreiro, José Brás, John Hardy, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|February 18, 2015
Multiple system atrophy: the application of genetics in understanding etiologyMonica Federoff, Lucia V Schottlaender, Henry Houlden, et al.
Medical Education|October 1, 2008
Learning not to take it seriously: junior doctors' accounts of errorLeanda Kroll, Andrew Singleton, Joe Collier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 3, 2011
Parkinson's disease and α-synuclein expressionMichael J Devine, Katrina Gwinn, Andrew Singleton, et al.
The FEBS Journal|November 22, 2008
Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body diseaseJose Bras, Andrew Singleton, Mark R Cookson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 31, 2012
DYT16: the original casesSarah Camargos, Andrew J Lees, Andrew Singleton, et al.
Human Mutation|December 19, 2009
A thorough assessment of benign genetic variability in GRN and MAPTRita J Guerreiro, Nicole Washecka, John Hardy, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 16, 2005
Prion genotypes in Central America suggest selection for the V129 alleleJohn Hardy, Sonja Scholz, Whitney Evans, et al.
Neuroscience Letters|August 28, 2004
Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish populationJordi Clarimon, Johanna Eerola, Olli Hellström, et al.
Alzheimer Disease and Associated Disorders|July 3, 2009
A case of dementia with PRNP D178Ncis-129M and no insomniaRita J Guerreiro, Tina Vaskov, Cynthia Crews, et al.
Pageof 29