View Author
scopus: 8074622400

Jansen, C.

(Casper Jansen)


disease patient prion mutation amyloid protein cortex brain plaque prpsc neuro fibrillary tangles netherland neuropathol deposit prion protein antibody prion protein gene creutzfeldt-jakob disease amyloid angiopathy codon creutzfeldt-jakob fragment analysis dementia prion disease cerebellum phenotype neuro nding residue fibrillary accumulation y 226x mutation q 227x mutation ??? angiopathy patient 2 tangle frontotemporal dementia disease duration variant examination change deposition blot analysis fi ndings centre feature prp-caa gss disease copyright © 2011 blood vessels g 131v mutation prion diseases american association parchi blood association tau accumulations amyloid depositions american result neuropathologist codon mutations month prion protein amyloidoses jansen tissue gerstmann-straussler-scheinker ¨ disease spongiform neurol 8- kd fragment variant creutzfeldt-jakob disease +++ number striatum neuro fibrillary lesions study multicentric amyloid plaques identi fied




3 Most Recent Publications

A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient (Article)
Jansen, C. Parchi, P. Capellari, S. Strammiello, R. Dopper, E.G.P. Swieten, J.C. van Kamphorst, W. Rozemuller, A.J.M.
2011-08-01
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
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