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Jessie Theuns

Showing results (1-10 of 45) with videos related to

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Neurology|January 2, 2008
alpha-Synuclein gene duplications in sporadic Parkinson diseaseJessie Theuns, Christine Van Broeckhoven
Archives of Neurology|May 29, 2012
The genetics of dementia with Lewy bodies: what are we missing?Bram Meeus, Jessie Theuns, Christine Van Broeckhoven
Human Mutation|May 15, 2012
Locus-specific mutation databases for neurodegenerative brain diseasesMarc Cruts, Jessie Theuns, Christine Van Broeckhoven
Trends in Genetics : TIG|February 24, 2015
Progress in unraveling the genetic etiology of Parkinson disease in a genomic eraAline Verstraeten, Jessie Theuns, Christine Van Broeckhoven
Journal of Chemical Neuroanatomy|August 4, 2011
Parkinson disease: insights in clinical, genetic and pathological features of monogenic disease subtypesDavid Crosiers, Jessie Theuns, Patrick Cras, et al.
Human Mutation|May 28, 2010
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation updateKaren Nuytemans, Jessie Theuns, Marc Cruts, et al.
Trends in Genetics : TIG|October 14, 2005
Tau is central in the genetic Alzheimer-frontotemporal dementia spectrumBart Dermaut, Samir Kumar-Singh, Rosa Rademakers, et al.
Parkinsonism & Related Disorders|November 25, 2010
Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutationDavid Crosiers, Berten Ceulemans, Bram Meeus, et al.
Human Molecular Genetics|April 2, 2003
Alzheimer-associated C allele of the promoter polymorphism -22C>T causes a critical neuron-specific decrease of presenilin 1 expressionJessie Theuns, Jacques Remacle, Richard Killick, et al.
Human Mutation|May 23, 2009
APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer diseaseKarolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Neurology|January 2, 2008
alpha-Synuclein gene duplications in sporadic Parkinson diseaseJessie Theuns, Christine Van Broeckhoven
Archives of Neurology|May 29, 2012
The genetics of dementia with Lewy bodies: what are we missing?Bram Meeus, Jessie Theuns, Christine Van Broeckhoven
Human Mutation|May 15, 2012
Locus-specific mutation databases for neurodegenerative brain diseasesMarc Cruts, Jessie Theuns, Christine Van Broeckhoven
Trends in Genetics : TIG|February 24, 2015
Progress in unraveling the genetic etiology of Parkinson disease in a genomic eraAline Verstraeten, Jessie Theuns, Christine Van Broeckhoven
Journal of Chemical Neuroanatomy|August 4, 2011
Parkinson disease: insights in clinical, genetic and pathological features of monogenic disease subtypesDavid Crosiers, Jessie Theuns, Patrick Cras, et al.
Human Mutation|May 28, 2010
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation updateKaren Nuytemans, Jessie Theuns, Marc Cruts, et al.
Trends in Genetics : TIG|October 14, 2005
Tau is central in the genetic Alzheimer-frontotemporal dementia spectrumBart Dermaut, Samir Kumar-Singh, Rosa Rademakers, et al.
Parkinsonism & Related Disorders|November 25, 2010
Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutationDavid Crosiers, Berten Ceulemans, Bram Meeus, et al.
Human Molecular Genetics|April 2, 2003
Alzheimer-associated C allele of the promoter polymorphism -22C>T causes a critical neuron-specific decrease of presenilin 1 expressionJessie Theuns, Jacques Remacle, Richard Killick, et al.
Human Mutation|May 23, 2009
APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer diseaseKarolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, et al.
Pageof 5