View Author
scopus: 7006466644

Boon, A.J.W.

(Andrea Boon)


patient study disease scale family shunt pressure score analysis dementia mutation outcome result table dystonia hydrocephalu control history group supranuclear palsy neurology region family history improvement value department syndrome neurol shunt placement shunting university onset pressure hydrocephalus factor nph scale outcome measures supranuclear deletion palsy parkin number difference disturbance measure tremor palatal myoclonus brain grade follow-up stage parkinson criteria nph scale score disorder examination gait disturbance linkage research infusion finding movement disease duration cerebrovascular disease palatal subject chapter myoclonu nph patients association diagnosis neurosurg protein placement month parkinsonism dementia scale gait scale fluid survival family members




10 Most Recent Publications

Phenotypes and genetic architecture of focal primary torsion dystonia (Article)
Groen, J.L. Kallen, M.C. Baas, F. Koning-Tijssen, M.A.J. de Warrenburg, B. van de Speelman, J.D. Hilten, J.J. van Aramideh, M. Boon, A.J.W. Klein, C. Koelman, J.H.T.M. Langeveld, T.P.M.
2012-10-01
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
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy (Article)
Hoglinger, G. Melhem, N.M. Swieten, J.C. van Pahwa, R. Pezzoli, G. Pickering-Brown, S. Poewe, W. Rabano, A. Rajput, A. Reich, S.G. Respondek, G. Roeber, S. Rohrer, J.D. Heutink, P. Ross, O.A. Rossor, M. Sacilotto, G. Seeley, W.W. Seppi, K. Silveira-Moriyama, L. Spina, S. Srulijes, K. St. George-Hyslop, P. Stamelou, M. Wszolek, Z.K. Standaert, D.G. Tesei, S. Tourtellotte, W.W. Trenkwalder, C. Troakes, C. Trojanowski, J.Q. Troncoso, J.C. Deerlin, V.M. Vonsattel, J.P.G. Wenning, G.K. Uitti, R.J. White, C.L. Winter, P. Zarow, C. Zecchinelli, A.L. Antonini, A. Vandrovcova, J. Hurtig, H.I. Gross, R.G. Maetzler, W. Goldwurm, S. Tolosa, E. Dickson, D. Borroni, B. Pastor, P. Cantwell, L.B. Han, M.R. Dillman, A. Brug, M.P. van der Gibbs, J. Cookson, M.R. Hernandez, D.G. Singleton, A. Sleiman, P.M.A. Farrer, M.J. Yu, C.-E. Golbe, L.I. Revesz, T. Hardy, J. Lees, A.J. Devlin, B. Hakonarson, H. Müller, U. Schellenberg, G.D. Wang, L.-S. Albin, R.L. Alonso, E. Apfelbacher, M. Arnold, S.E. Avila, J. Beach, T.G. Beecher, S. Berg, D. Bird, T.D. Bogdanovic, N. Klei, L. Boon, A.J.W. Bordelon, Y. Brice, A. Budka, H. Canesi, M. Chiu, W.Z. Cilia, R. Colosimo, C. Deyn, P.P. de Yebenes, J.G. de Rademakers, R. Donker Kaat, L. Duara, R. Durr, A. Engelborghs, S. Fabbrini, G. Finch, N.A. Flook, R. Frosch, M.P. Gaig, C. Galasko, D. Silva, R. de Gasser, T. Gearing, M. Geller, E.T. Ghetti, B. Graff-Radford, N.R. Grossman, M. Hall, D.A. Hazrati, L.-N. Höllerhage, M. Jankovic, J. Litvan, I. Juncos, J.L. Karydas, A. Kretzschmar, H.A. Leber, I. Lee, V.M.Y. Lieberman, A.P. Lyons, K.E. Mariani, C. Masliah, E. Massey, L.A. Riley, D.E. McLean, C.A. Meucci, N. Miller, B.L. Mollenhauer, B. Möller, J.C. Morris, H. O'Sullivan, S.S. Oertel, W. Ottaviani, D. Padovani, A.
2011-07-01
Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred (Article)
Sas, A.M.G. Fonzo, A. di Bakker, S.L.M. Simons, E.J. Oostra, B.A. Maat-Kievit, A.A. Boon, A.J.W. Bonifati, V.
2010-08-15
Survival in progressive supranuclear palsy and frontotemporal dementia (Article)
Chiu, W.Z. Donker Kaat, L. Seelaar, H. Rosso, S.M. Boon, A.J.W. Kamphorst, W. Swieten, J.C. van
2010-04-01
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
A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier? (Article)
Brusse, E. Majoor-Krakauer, D.F. Graaf, B.M. de Visser, G.H. Swagemakers, S.M.A. Boon, A.J.W. Oostra, B.A. Bertoli Avella, A.M.
2009-04-27
New device to control combined lingual and palatal myoclonus (Article)
Mondria, T. Gier, H.H.W. de Boon, A.J.W.
2007-03-15
Blue rubber bleb nevus syndrome (Article)
Heijer, T. den Boon, A.J.W.
2007-03-01
The Dutch Normal-Pressure Hydrocephalus Study (Doctoral Thesis)
Boon, A.J.W.
1999-03-31