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Showing results (21-30 of 31) with videos related to

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Brain : a Journal of Neurology|May 8, 2004
Familial clustering and genetic risk for dementia in a genetically isolated Dutch populationK Sleegers, G Roks, J Theuns, et al.
Neurology|February 18, 2011
Cerebrovascular risk factors and preclinical memory decline in healthy APOE ε4 homozygotesR J Caselli, A C Dueck, D E C Locke, et al.
European Journal of Neurology|February 17, 2015
Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance imagesJ L Whitwell, B F Boeve, S D Weigand, et al.
Neurology|April 11, 2008
Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotypeK A Josephs, J L Whitwell, D S Knopman, et al.
Neurology|August 19, 2011
Altered functional connectivity in asymptomatic MAPT subjects: a comparison to bvFTDJ L Whitwell, K A Josephs, R Avula, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 21, 2007
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypesJ C Schymick, Y Yang, P M Andersen, et al.
Neurology|June 10, 2009
Characterization of DCTN1 genetic variability in neurodegenerationC Vilariño-Güell, C Wider, A I Soto-Ortolaza, et al.
Neurology|March 14, 2008
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson diseaseK Haugarvoll, R Rademakers, J M Kachergus, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 9, 2020
Active lifestyles moderate clinical outcomes in autosomal dominant frontotemporal degenerationK B Casaletto, A M Staffaroni, A Wolf, et al.
Neurology|December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN Finch, M M Carrasquillo, M Baker, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Brain : a Journal of Neurology|May 8, 2004
Familial clustering and genetic risk for dementia in a genetically isolated Dutch populationK Sleegers, G Roks, J Theuns, et al.
Neurology|February 18, 2011
Cerebrovascular risk factors and preclinical memory decline in healthy APOE ε4 homozygotesR J Caselli, A C Dueck, D E C Locke, et al.
European Journal of Neurology|February 17, 2015
Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance imagesJ L Whitwell, B F Boeve, S D Weigand, et al.
Neurology|April 11, 2008
Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotypeK A Josephs, J L Whitwell, D S Knopman, et al.
Neurology|August 19, 2011
Altered functional connectivity in asymptomatic MAPT subjects: a comparison to bvFTDJ L Whitwell, K A Josephs, R Avula, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 21, 2007
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypesJ C Schymick, Y Yang, P M Andersen, et al.
Neurology|June 10, 2009
Characterization of DCTN1 genetic variability in neurodegenerationC Vilariño-Güell, C Wider, A I Soto-Ortolaza, et al.
Neurology|March 14, 2008
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson diseaseK Haugarvoll, R Rademakers, J M Kachergus, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 9, 2020
Active lifestyles moderate clinical outcomes in autosomal dominant frontotemporal degenerationK B Casaletto, A M Staffaroni, A Wolf, et al.
Neurology|December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN Finch, M M Carrasquillo, M Baker, et al.
Pageof 4