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Sarah Lincoln

Showing results (11-20 of 35) with videos related to

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Neurology|February 1, 2013
DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing lossChristopher J Klein, Tom Bird, Nilufer Ertekin-Taner, et al.
Annals of Neurology|February 3, 2004
Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplicationsMatt Farrer, Jennifer Kachergus, Lysia Forno, et al.
Annals of Neurology|September 30, 2004
alpha-Synuclein promoter confers susceptibility to Parkinson's diseasePhilippe Pals, Sarah Lincoln, Jonathan Manning, et al.
Neuroscience Letters|May 11, 2005
UCHL1 is associated with Parkinson's disease: a case-unaffected sibling and case-unrelated control studyMaurizio Facheris, Kari J Strain, Timothy G Lesnick, et al.
Lancet (London, England)|September 29, 2004
Alpha-synuclein locus duplication as a cause of familial Parkinson's diseaseMarie-Christine Chartier-Harlin, Jennifer Kachergus, Christophe Roumier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2002
Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutationsRuey-Meei Wu, Din-E Shan, Chen-Ming Sun, et al.
Neuroscience Letters|July 4, 2009
GCH1 expression in human cerebellum from healthy individuals is not gender dependentChristian Wider, Sarah Lincoln, Justus C Dachsel, et al.
Neurogenetics|September 21, 2005
Lrrk2 pathogenic substitutions in Parkinson's diseaseIgnacio F Mata, Jennifer M Kachergus, Julie P Taylor, et al.
American Journal of Medical Genetics|July 13, 2002
Complex relationship between Parkin mutations and Parkinson diseaseAndrew West, Magali Periquet, Sarah Lincoln, et al.
Neurology. Genetics|January 20, 2022
Clinical Deep Phenotyping of <i>ABCA7</i> Mutation CarriersAlana S Campbell, Charlotte C G Ho, Merve Atık, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Neurology|February 1, 2013
DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing lossChristopher J Klein, Tom Bird, Nilufer Ertekin-Taner, et al.
Annals of Neurology|February 3, 2004
Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplicationsMatt Farrer, Jennifer Kachergus, Lysia Forno, et al.
Annals of Neurology|September 30, 2004
alpha-Synuclein promoter confers susceptibility to Parkinson's diseasePhilippe Pals, Sarah Lincoln, Jonathan Manning, et al.
Neuroscience Letters|May 11, 2005
UCHL1 is associated with Parkinson's disease: a case-unaffected sibling and case-unrelated control studyMaurizio Facheris, Kari J Strain, Timothy G Lesnick, et al.
Lancet (London, England)|September 29, 2004
Alpha-synuclein locus duplication as a cause of familial Parkinson's diseaseMarie-Christine Chartier-Harlin, Jennifer Kachergus, Christophe Roumier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2002
Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutationsRuey-Meei Wu, Din-E Shan, Chen-Ming Sun, et al.
Neuroscience Letters|July 4, 2009
GCH1 expression in human cerebellum from healthy individuals is not gender dependentChristian Wider, Sarah Lincoln, Justus C Dachsel, et al.
Neurogenetics|September 21, 2005
Lrrk2 pathogenic substitutions in Parkinson's diseaseIgnacio F Mata, Jennifer M Kachergus, Julie P Taylor, et al.
American Journal of Medical Genetics|July 13, 2002
Complex relationship between Parkin mutations and Parkinson diseaseAndrew West, Magali Periquet, Sarah Lincoln, et al.
Neurology. Genetics|January 20, 2022
Clinical Deep Phenotyping of <i>ABCA7</i> Mutation CarriersAlana S Campbell, Charlotte C G Ho, Merve Atık, et al.
Pageof 4