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R Rademakers

Showing results (11-20 of 31) with videos related to

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Neurobiology of Aging|May 27, 2005
Association of cyclin-dependent kinase 5 and neuronal activators p35 and p39 complex in early-onset Alzheimer's diseaseR Rademakers, K Sleegers, J Theuns, et al.
Journal of Neurology|January 5, 2002
Variable expression of presenilin 1 is not a major determinant of risk for late-onset Alzheimer's diseaseB Dermaut, G Roks, J Theuns, et al.
Neuropathology and Applied Neurobiology|November 19, 2016
Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathyP Tacik, M Sanchez-Contreras, M DeTure, et al.
Neurology|April 12, 2012
Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulinE McDade, B F Boeve, T M Burrus, et al.
European Journal of Neurology|May 29, 2009
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's diseaseB Jasinska-Myga, C Wider, G Opala, et al.
Neurology|September 30, 2009
Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutationsJ L Whitwell, C R Jack, B F Boeve, et al.
Neurology|March 4, 2009
Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRNJ L Whitwell, C R Jack, B F Boeve, et al.
Neurology|December 22, 2010
Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?J L Whitwell, C R Jack, J E Parisi, et al.
Neurology|September 1, 2010
MRS in presymptomatic MAPT mutation carriers: a potential biomarker for tau-mediated pathologyK Kantarci, B F Boeve, Z K Wszolek, et al.
Neurology|July 15, 2011
Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRNJ L Whitwell, S D Weigand, J L Gunter, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Neurobiology of Aging|May 27, 2005
Association of cyclin-dependent kinase 5 and neuronal activators p35 and p39 complex in early-onset Alzheimer's diseaseR Rademakers, K Sleegers, J Theuns, et al.
Journal of Neurology|January 5, 2002
Variable expression of presenilin 1 is not a major determinant of risk for late-onset Alzheimer's diseaseB Dermaut, G Roks, J Theuns, et al.
Neuropathology and Applied Neurobiology|November 19, 2016
Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathyP Tacik, M Sanchez-Contreras, M DeTure, et al.
Neurology|April 12, 2012
Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulinE McDade, B F Boeve, T M Burrus, et al.
European Journal of Neurology|May 29, 2009
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's diseaseB Jasinska-Myga, C Wider, G Opala, et al.
Neurology|September 30, 2009
Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutationsJ L Whitwell, C R Jack, B F Boeve, et al.
Neurology|March 4, 2009
Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRNJ L Whitwell, C R Jack, B F Boeve, et al.
Neurology|December 22, 2010
Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?J L Whitwell, C R Jack, J E Parisi, et al.
Neurology|September 1, 2010
MRS in presymptomatic MAPT mutation carriers: a potential biomarker for tau-mediated pathologyK Kantarci, B F Boeve, Z K Wszolek, et al.
Neurology|July 15, 2011
Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRNJ L Whitwell, S D Weigand, J L Gunter, et al.
Pageof 4