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scopus: 6602721302

Rozemuller, A.J.M.

(Annemieke Rozemuller)


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




5 Most Recent Publications

Symmetrical corticobasal syndrome caused by a novel c.314dup progranulin mutation (Article)
Dopper, E.G.P. Seelaar, H. Chiu, W.Z. Koning, I. de Minkelen, R. van Baker, M.C. Rozemuller, A.J.M. Rademakers, R. Swieten, J.C. van
2011-11-01
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
Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP (Article)
Jansen, C. Parchi, P. Capellari, S. Vermeij, A.J. Corrado, P. Baas, F. Strammiello, R. Gool, W.A. van Swieten, J.C. van Rozemuller, A.J.M.
2010-02-01
Rab6 is increased in Alzheimer's disease brain and correlates with endoplasmic reticulum stress (Article)
Scheper, W. Hoozemans, J.J.M. Hoogenraad, C.C. Rozemuller, A.J.M. Eikelenboom, P. Baas, F.
2007-10-01
The first case of variant Creutzfeldt-Jakob disease in the Netherlands [6] (Article)
Sanchez-Juan, P. Houben, M.P.W.A. Hoff, J.I. Jansen, C. Sie, M.P.S. Rijn, M.J.E. van Ironside, J.W. Will, R.G. Tikka-Kleemola, P. Rozemuller, A.J.M.
2007-07-01