Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Richard J. Beukers"'
Autor:
Richard J. Beukers, Maria Fiorella Contarino, Hans D Speelman, P. Rick Schuurman, Jan eBooij, Marina A.J. Tijssen
Publikováno v:
Frontiers in Neurology, Vol 3 (2012)
Purpose: To assess clinical efficacy of deep brain stimulation of the pallidum in Myoclonus-Dystonia patients, and to compare pre- and postoperative striatal dopamine D2 receptor availability.Methods: Clinical parameters were scored using validated r
Externí odkaz:
https://doaj.org/article/2fcfa9b8bc04498096818e725712d65e
Autor:
Richard J. Beukers, Marina A. J. Tijssen, S. M. A. van der Salm, Aart J. Nederveen, Matthan W.A. Caan, Johan N. van der Meer
Publikováno v:
Movement Disorders. 27:1666-1672
Myoclonus-dystonia is an autosomal dominantly inherited movement disorder clinically characterized by myoclonic jerks and dystonic movements of the upper body. Functional imaging and structural gray matter imaging studies in M-D suggest defective sen
Autor:
S. M. A. van der Salm, J.N. van der Meer, Dick J. Veltman, Elisabeth M. J. Foncke, Marina A. J. Tijssen, Richard J. Beukers
Publikováno v:
European Journal of Neurology. 18:906-912
Background: Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder characterized by myoclonic jerks and dystonic postures or movements. Morphometric studies have been performed in other, mainly heterogenous, types of dystonia
Autor:
Michiel B. de Ruiter, Elisabeth M. J. Foncke, Johan N. van der Meer, Richard J. Beukers, Marina A. J. Tijssen, Dick J. Veltman, Lo J. Bour, Aart J. Nederveen
Publikováno v:
Archives of Neurology, 67(4), 469-474. American Medical Association
Archives of Neurology, 67(4), 469-474. AMER MEDICAL ASSOC
Archives of neurology, 67(4), 469-474. American Medical Association
Beukers, R J, Foncke, E M J, van der Meer, J N, Nederveen, A J, de Ruiter, M B, Bour, L J, Veltman, D J & Tijssen, M A J 2010, ' Disorganized Sensorimotor Integration in Mutation-Positive Myoclonus-Dystonia A Functional Magnetic Resonance Imaging Study ', Archives of Neurology, vol. 67, no. 4, pp. 469-474 . https://doi.org/10.1001/archneurol.2010.54
Archives of Neurology, 67(4), 469-474. AMER MEDICAL ASSOC
Archives of neurology, 67(4), 469-474. American Medical Association
Beukers, R J, Foncke, E M J, van der Meer, J N, Nederveen, A J, de Ruiter, M B, Bour, L J, Veltman, D J & Tijssen, M A J 2010, ' Disorganized Sensorimotor Integration in Mutation-Positive Myoclonus-Dystonia A Functional Magnetic Resonance Imaging Study ', Archives of Neurology, vol. 67, no. 4, pp. 469-474 . https://doi.org/10.1001/archneurol.2010.54
Background: Myoclonus-dystonia is an autosomal dominantly inherited movement disorder clinically characterized by myoclonic jerks and dystonic postures or movements of the upper body. Functional imaging studies in other, mainly heterogeneous groups o
Autor:
Fleur Zijlstra, T. van Amelsvoort, N. Weisscher, Richard J. Beukers, Jan Booij, Marina A. J. Tijssen
Publikováno v:
European Journal of Nuclear Medicine and Molecular Imaging, 36(2), 269-274. SPRINGER
European Journal of Nuclear Medicine and Molecular Imaging, 36(2), 269-274. Springer Verlag
European journal of nuclear medicine and molecular imaging, 36(2), 269-274. Springer Verlag
European Journal of Nuclear Medicine and Molecular Imaging, 36(2), 269-274. Springer Verlag
European journal of nuclear medicine and molecular imaging, 36(2), 269-274. Springer Verlag
Purpose To study striatal dopamine D-2 receptor availability in DYT11 mutation carriers of the autosomal dominantly inherited disorder myoclonus-dystonia (M-D).Methods Fifteen DYT11 mutation carriers ( 11 clinically affected) and 15 age- and sex-matc
Autor:
Johan N, van der Meer, Richard J, Beukers, S M A, van der Salm, Matthan W A, Caan, Marina A J, Tijssen, Aart J, Nederveen
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 27(13)
Myoclonus-dystonia is an autosomal dominantly inherited movement disorder clinically characterized by myoclonic jerks and dystonic movements of the upper body. Functional imaging and structural gray matter imaging studies in M-D suggest defective sen
Autor:
Marina A. J. Tijssen, Johannes D. Speelman, Jan Booij, P.R. Schuurman, Richard J. Beukers, Maria Fiorella Contarino
Publikováno v:
Frontiers in Neurology
Frontiers in neurology, 3. Frontiers Media S.A.
ResearcherID
Frontiers in Neurology, Vol 3 (2012)
Frontiers in neurology, 3. Frontiers Media S.A.
ResearcherID
Frontiers in Neurology, Vol 3 (2012)
Purpose: To assess clinical efficacy of deep brain stimulation of the pallidum in Myoclonus-Dystonia patients, and to compare pre- and postoperative striatal dopamine D2 receptor availability. Methods: Clinical parameters were scored using validated
Autor:
Johan N. van der Meer, Elisabeth M. J. Foncke, Marina A. J. Tijssen, Richard J. Beukers, Dick J. Veltman
Publikováno v:
Archives of neurology, 68(6), 802-805. American Medical Association
Beukers, R J, Foncke, E M J, van der Meer, J N, Veltman, D J & Tijssen, M A 2011, ' Functional Magnetic Resonance Imaging Evidence of Incomplete Maternal Imprinting in Myoclonus-Dystonia ', Archives of Neurology, vol. 68, no. 6, pp. 802-805 . https://doi.org/10.1001/archneurol.2011.23
Archives of Neurology, 68(6), 802-805. American Medical Association
Archives of Neurology, 68(6), 802-805. AMER MEDICAL ASSOC
Beukers, R J, Foncke, E M J, van der Meer, J N, Veltman, D J & Tijssen, M A 2011, ' Functional Magnetic Resonance Imaging Evidence of Incomplete Maternal Imprinting in Myoclonus-Dystonia ', Archives of Neurology, vol. 68, no. 6, pp. 802-805 . https://doi.org/10.1001/archneurol.2011.23
Archives of Neurology, 68(6), 802-805. American Medical Association
Archives of Neurology, 68(6), 802-805. AMER MEDICAL ASSOC
Background: Myoclonus-dystonia is an autosomal dominantly inherited movement disorder, clinically characterized by myoclonic jerks and dystonic postures or movements. A previous functional magnetic resonance imaging study showed altered cortical acti
Autor:
Cees C. Tijssen, Johannes H. T. M. Koelman, Marina A. J. Tijssen, Elisabeth M. J. Foncke, Richard J. Beukers
Publikováno v:
Parkinsonism & Related Disorders, 16(4), 288-289. Elsevier
Foncke, E M J, Beukers, R J, Tijssen, C C, Koelman, J H & Tijssen, M A 2010, ' Myoclonus-dystonia and spinocerebellar ataxia type 14 presenting with similar phenotypes: Trunk tremor, myoclonus, and dystonia ', Parkinsonism and Related Disorders, vol. 16, no. 4, pp. 288-289 . https://doi.org/10.1016/j.parkreldis.2009.10.008
Parkinsonism and Related Disorders, 16(4), 288-289. Elsevier BV
Parkinsonism & related disorders, 16(4), 288-289. Elsevier BV
Foncke, E M J, Beukers, R J, Tijssen, C C, Koelman, J H & Tijssen, M A 2010, ' Myoclonus-dystonia and spinocerebellar ataxia type 14 presenting with similar phenotypes: Trunk tremor, myoclonus, and dystonia ', Parkinsonism and Related Disorders, vol. 16, no. 4, pp. 288-289 . https://doi.org/10.1016/j.parkreldis.2009.10.008
Parkinsonism and Related Disorders, 16(4), 288-289. Elsevier BV
Parkinsonism & related disorders, 16(4), 288-289. Elsevier BV
We describe three genetically confirmed myoclonus dystonia (M-D) patients and one spinocerebellar ataxia type 14 (SCA14) patient, presenting with a combination of trunk tremor, multifocal myoclonus and axial dystonia as predominant clinical features.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4285afc5c9d0f4941322fd0114331ec6
https://research.rug.nl/en/publications/fae107ce-6aa7-4bdb-ae9f-fb0bcf6b6823
https://research.rug.nl/en/publications/fae107ce-6aa7-4bdb-ae9f-fb0bcf6b6823
Autor:
Wouterina C.G. Overweg-Plandsoen, Mariken Gruppen, Marinus Vermeulen, Annemarie C.M. van Bellegem, Richard J. Beukers
Publikováno v:
Pediatric neurology, 42(4), 301-303. Elsevier Inc.
A case of acute predominantly axonal motor and sensory neuropathy (AMSAN) is reported in a 16-year-old boy with LEOPARD syndrome (the acronym represents lentigines, ECG conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef782369ada54ce308e741ea4d1d1ae
https://pure.amc.nl/en/publications/acute-motor-and-sensory-axonal-neuropathy-in-leopard-syndrome(6308dffc-c1c0-47e2-8346-6f171ecb2b01).html
https://pure.amc.nl/en/publications/acute-motor-and-sensory-axonal-neuropathy-in-leopard-syndrome(6308dffc-c1c0-47e2-8346-6f171ecb2b01).html