View Author
patient caudate atrophy atrophy ftld-fu caudate family history inclusion onset frontotemporal lobar degeneration frontotemporal brain history family degeneration dementia disease caudate nucleus bvftd mutation ftld-u lobar frontotemporal dementia ftld-fus cases -43 -43-negative feature ubiquitin study subtype neurol motor neuron disease frequency ?? ?? filament inclusion disease protein executive functions substantia nigra ubiquitin-positive antibody tdp -43 nucleus neuron b 50 years tdp -43-negative inclusions percent center rotterdam netherland pathology cytoplasmatic inclusions intranuclear inclusions neuropathol immunohistochemistry tdp -43-negative ftld-u cases department cohort function fus-positive substantia attention staining ftldfu rotterdam group behavioural nigra neuropathological sclerosis center inclusion body disease erasmus mc concentration ftld-tdp ubiquitin-positive inclusions behavioural variant ftd dentate gyrus fus antibody netherlands brain bank examination pd-weighted mr image
6 Most Recent Publications
|
Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration
(Article)
Seelaar, H. Klijnsma, K.Y. Koning, I. de Lugt, A. van der Chiu, W.Z. Azmani, A. Rozemuller, A.J.M. Swieten, J.C. van |
2010-05-01
|
|
Familial aggregation of parkinsonism in progressive supranuclear palsy
(Article)
Donker Kaat, L. Boon, A.J.W. Azmani, A. Kamphorst, W. Breteler, M.M.B. Anar, B. Heutink, P. Swieten, J.C. van |
2009-07-01
|
|
Distinct genetic forms of frontotemporal dementia.
(Article)
Seelaar, H. Kamphorst, W. Dooijes, D. Rozemuller, J.M. Bronner, I.F. Rizzu, P. Swieten, J.C. van Rosso, S.M. Azmani, A. Masdjedi, R. Koning, I. de Maat-Kievit, A.A. Anar, B. Donker Kaat, L. Breedveld, G.J. |
2008-10-14
|
|
TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations
(Article)
Seelaar, H. Jurgen Schelhaas, H. Kamphorst, W. Willemsen, R. Swieten, J.C. van Azmani, A. Küsters, B. Rosso, S.M. Majoor-Krakauer, D.F. Rijik, M.C. de Rizzu, P. Brummelhuis, M. ten Doorn, P.A. van |
2007-05-01
|
|
Progranulin mutations in Dutch familial frontotemporal lobar degeneration
(Article)
Bronner, I.F. Rizzu, P. Seelaar, H. Mil, S.E. van Anar, B. Azmani, A. Donker Kaat, L. Rosso, S.M. Heutink, P. Swieten, J.C. van |
2007-03-01
|
|
The ΔK280 mutation in MAP tau favors exon 10 skipping in vivo
(Article)
Swieten, J.C. van Bronner, I.F. Azmani, A. Severijnen, L.A. Kamphorst, W. Ravid, R. Rizzu, P. Willemsen, R. Heutink, P. |
2007-01-01
|