Swieten, J.C. van

( J.C. van Swieten)

patient disease mutation dementia study frontotemporal frontotemporal dementia alzheimer family brain protein frontotemporal lobar degeneration association onset neurology analysis control neurol pathology sample caregiver chromosome table university inclusion degeneration level region criteria netherland rotterdam research department population family history effect bvftd alzheimer disease parkinsonism lobar neuron score diagnosis symptom feature number ataxia function atrophy factor signi antibody group allele center disorder result progranulin amyloid motor genet variant supranuclear palsy expression ftld-tdp history linkage individual model cohort syndrome change motor neuron disease grn mutations behavioural rotterdam study -43 erasmu genotype marker

10 Most Recent Publications

Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS (Article) Ravenscroft, T.A. Baker, M.C. Swieten, J.C. van Seeley, W.W. Dickson, D.W. Rademakers, R. Rutherford, N.J. Neumann, H.A.M. Mackenzie, I.R.A. Josephs, K.A. Boeve, B. Petersen, R.C. Halliday, G.M. Kril, J.J.	2013-04-29
Blood-brain barrier P-glycoprotein function in healthy subjects and Alzheimer's disease patients: Effect of polymorphisms in the ABCB1 gene (Article) Assema, D.M.E. van Lubberink, M. Rizzu, P. Swieten, J.C. van Schuit, R.C. Eriksson, J. Scheltens, P. Koepp, M. Lammertsma, A.A. Berckel, B.N.M. van	2012-12-01
Development and assessment of sensitive immuno-PCR assays for the quantification of cerebrospinal fluid three- and four-repeat tau isoforms in tauopathies (Article) Luk, C. Compta, Y. Trenkwalder, C. Swieten, J.C. van Chiu, W.Z. Borroni, B. Cámara, A. Cheshire, P. Williams, D.R. Lees, A.J. Silva, R. de Magdalinou, N. Martí, M.J. Hondhamuni, G. Zetterberg, H. Blennow, K. Constantinescu, R. Pijnenburg, Y. Mollenhauer, B.	2012-11-01
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
Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations (Article) Elfferich, P.C. Verleun-Mooijman, M.C. Swieten, J.C. van Boon, A.J.W. Engelen, K. van Verschuuren-Bemelmans, C.C. Lesnik-Oberstein, S.A.J. Tassorelli, C. Lopiano, L. Bonifati, V. Dooijes, D. Minkelen, R. van Maat-Kievit, A.A. Warrenburg, B. van de Abdo, W.F. Eshuis, S.A. Leenders, K.L. Hovestadt, A. Zijlmans, J.C.M. Stroy, J.-P.M.	2011-11-01
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD (Article) Renton, A. Majounie, E. Kalimo, H. Paetau, A. Abramzon, Y. Remes, A. Kaganovich, A. Scholz, S. Duckworth, J. Ding, J. Harmer, D. Hernandez, D.G. Waite, A. Johnson, J. Mok, K. Ryten, M. Trabzuni, D. Guerreiro, R. Orrell, R. Neal, J. Murray, A. Pearson, J. Jansen, I. Simón-Sánchez, J. Sondervan, D. Seelaar, H. Blake, D. Young, K. Halliwell, N. Callister, J. Toulson, G. Richardson, A. Gerhard, A. Snowden, J. Rollinson, S. Mann, D. Neary, D. Nalls, M.A. Peuralinna, T. Jansson, L. Isoviita, V.-M. Kaivorinne, A.-L. Hölttä-Vuori, M. Ikonen, E. Sulkava, R. Gibbs, J. Benatar, M. Wuu, J. Chiò, A. Restagno, G. Borghero, G. Sabatelli, M. Heckerman, D. Rogaeva, E. Zinman, L. Rothstein, J. Schymick, J. Sendtner, M. Drepper, C. Eichler, E. Alkan, C. Abdullaev, Z. Pack, S. Dutra, A. Pak, E. Hardy, J. Singleton, A. Laaksovirta, H. Williams, N. Heutink, P. Pickering-Brown, S. Morris, H. Tienari, P.J. Traynor, B. Swieten, J.C. van Myllykangas, L.	2011-10-20
Cathepsin D gene and the risk of Alzheimer's disease: A population-based study and meta-analysis (Article) Schuur, M. Ikram, M.A. Swieten, J.C. van Isaacs, A. Vergeer-Drop, J. Hofman, B. Oostra, B.A. Breteler, M.M.B. Duijn, C.M. van	2011-09-01
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia (Article) Rascovsky, K. Hodges, J. Hillis, A.E. Josephs, K.A. Boeve, B.F. Kertesz, A. Seeley, W.W. Rankin, K.P. Johnson, J.K. Gorno-Tempini, M.-L. Rosen, H. Prioleau-Latham, C.E. Knopman, D.S. Lee, A. Kipps, C.M. Lillo, P. Piguet, O. Rohrer, J.D. Rossor, M. Warren, J.D. Fox, N.C. Galasko, D. Salmon, D.P. Mendez, M.F. Black, S.E. Mesulam, M. Weintraub, S. Dickerson, B.C. Diehl-Schmid, J. Pasquier, F. Deramecourt, V. Lebert, F. Pijnenburg, Y. Chow, T.W. Kramer, J.H. Manes, F. Grafman, J. Cappa, S.F. Freedman, M. Grossman, M. Miller, B.L. Neuhaus, J. Swieten, J.C. van Seelaar, H. Dopper, E.G.P. Onyike, C.U.	2011-09-01
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
Brain perfusion patterns in familial frontotemporal lobar degeneration (Article) Seelaar, H. Papma, J.M. Garraux, G. Koning, I. de Reijs, A.E.M. Valkema, R. Rozemuller, A.J.M. Salmon, E. Swieten, J.C. van	2011-07-26

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