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scopus: 35072383300

Visser, M. de

(Marianne de Visser)


patient mutation study anisotropy disease corticospinal tract bulbar-onset als diffusion tract limb-onset als control analysis tensor corticospinal motoneuron imaging signi ficantly neck pain table neurology motor nerve bulbar-onset matter sclerosis signi limb-onset diffusion tensor tractography root compression department value compression corpus callosum baseline netherland amyotrophic university diffusion tensor imaging p.a 467t mutation agreement phenotype anisotropy reduction voxel-based family brain genome-wide motoneuron disease phenotypes polg mutations ficantly group kappa voxel-based analysis study sample carrier radiculopathy involvement reduction result capsule voxel-based analysis institute cortex mitochondrial right tractography cohort variant anisotropy values motoneuron disease association onset replication illumina patient groups change callosum follow-up corpus feature downloaded




6 Most Recent Publications

The phenotype of the Gly94fsX222 PMP22 insertion (Article)
Vries, S.D.J. de Verhamme, C. Baas, F. Ruissen, F. van Paassen, B.W. van Arts, W.F.M. Kerkhoff, H. Engelen, B.G.M. van Lammens, M. Visser, M. de Kooi, A.J. van der
2011-06-01
Upper and extra-motoneuron involvement in early motoneuron disease: A diffusion tensor imaging study (Article)
Graaff, M.M. van der Sage, C.A. Berg, L.H. van den Rijk, M.C. de Doorn, P.A. van Hecke, W. van Peeters, R.R. Robberecht, W. Sunaert, S.G. Visser, M. de Caan, M.W.A. Akkerman, E.M. Lavini, C. Majoie, C.B. Nederveen, A.J. Zwinderman, A.H. Vos, F. Brugman, F.
2011-04-01
Interobserver agreement on MRI evaluation of patients with cervical radiculopathy (Article)
Kuijper, B. Beelen, A. Kallen, B.F.W. van der Nollet, F. Lycklama à Nijeholt, G.J. Visser, M. de Tans, J.T.
2011-01-01
Cervical collar or physiotherapy versus wait and see policy for recent onset cervical radiculopathy: randomised trial. (Article)
Kuijper, B. Tans, J.T. Beelen, A. Nollet, F. Visser, M. de
2009-11-03
The unfolding clinical spectrum of POLG mutations (Article)
Blok, M.J. Bosch, B.J. van den Coo, I.F.M. de Smeets, H.J. Jongen, E. Hendrickx, A. Die-Smulders, C. de Hoogendijk, J.E. Brusse, E. Visser, M. de Poll-The, B.T. Bierau, J.
2009-11-01
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis (Article)
Es, M.A. van Veldink, J.H. Kooi, A.J. van der Visser, M. de Dahlberg, C. Estrada Gil, J.K. Rivadeneira Ramirez, F. Hofman, A. Zwarts, M.J. Doormaal, P.T.C. van Rujescu, D. Strengman, E. Saris, C.G. Giegling, I. Muglia, P. Tomik, B. Slowik, A. Uitterlinden, A.G. Hendrich, C. Waibel, S. Meyer, T. Ludolph, A.C. Glass, J.D. Blauw, H.M. Purcell, S. Cichon, S. Nöthen, M.M. Wichmann, H.E. Schreiber, S. Vermeulen, S.H.H.M. Kiemeney, L.A.L.M. Wokke, J.H.J. Cronin, S. Mclaughlin, R.L. Vught, P.W. van Hardiman, O. Fumoto, K. Pasterkamp, R.J. Meininger, V. Melki, J. Leigh, P.N. Shaw, C.E. Landers, J.E. Al-Chalabi, A. Brown Jr, R.H. Birve, A. Robberecht, W. Andersen, P.M. Ophoff, R.A. Berg, L.H. van den Lemmens, R. Schelhaas, H.J. Groen, E.J. Huisman, M.H.B.
2009-10-01