Zobrazeno 1 - 7
of 7
pro vyhledávání: '"S. M. A. van der Salm"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82d30e7f95b0f28c50977e209be153ba
https://doi.org/10.1002/mds.25128
https://doi.org/10.1002/mds.25128
Autor:
Maria Fiorella Contarino, S. M. A. van der Salm, Danielle C. Cath, E.M.J. Foncke, Yasmine E. M. Dreissen, M.J. van Tricht, Justus L. Groen, Joke M. Dijk, Marina A. J. Tijssen, Ben Schmand
Publikováno v:
van Tricht, M J, Dreissen, Y E M, Cath, D, Dijk, J M, Contarino, M F, van der Salm, S M, Foncke, E M J, Groen, J L, Schmand, B & Tijssen, M A J 2012, ' Cognition and psychopathology in myoclonus-dystonia ', Journal of Neurology, Neurosurgery and Psychiatry, vol. 83, no. 8, pp. 814-820 . https://doi.org/10.1136/jnnp-2011-301386
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 83(8), 814-820. BMJ PUBLISHING GROUP
Journal of Neurology, Neurosurgery and Psychiatry, 83(8), 814-820. BMJ Publishing Group
Journal of neurology, neurosurgery, and psychiatry, 83(8), 814-820. BMJ Publishing Group
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 83(8), 814-820. BMJ PUBLISHING GROUP
Journal of Neurology, Neurosurgery and Psychiatry, 83(8), 814-820. BMJ Publishing Group
Journal of neurology, neurosurgery, and psychiatry, 83(8), 814-820. BMJ Publishing Group
Objective (1) To study the neuropsychological and psychopathological profile in myoclonus-dystonia (M-D) patients with and without a mutation in the DYT11 gene. (2) To explore whether cognitive and psychiatric impairments are related to severity and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d037c8663812f5b02a98fff78f57760
https://doi.org/10.1136/jnnp-2011-301386
https://doi.org/10.1136/jnnp-2011-301386
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f6c372977c1d59ff8ba0df76d30812
https://doi.org/10.1111/j.1468-1331.2010.03321.x
https://doi.org/10.1111/j.1468-1331.2010.03321.x
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::955a853a021a918a54afa0111388f1fa
https://pubmed.ncbi.nlm.nih.gov/23114862
https://pubmed.ncbi.nlm.nih.gov/23114862
Autor:
Elisabeth M. J. Foncke, Kailash P. Bhatia, John C. Rothwell, Lo J. Bour, A.F. van Rootselaar, Johannes H. T. M. Koelman, Marina A. J. Tijssen, S. M. A. van der Salm
Publikováno v:
Experimental Neurology, 216(2), 300-305. ACADEMIC PRESS INC JNL-COMP SUBSCRIPTIONS
Experimental neurology, 216(2), 300-305. Academic Press Inc.
Experimental neurology, 216(2), 300-305. Academic Press Inc.
Objective: The aim of the present study is to investigate cortical excitability in patients with DYT 11 positive Myoclonus-Dystonia (M-D), using transcranial magnetic stimulation (TMS).Methods: Silent period, motor evoked potential (MEP) recruitment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9a87c16cf905b75e98b2de7c50cc2a0
https://pubmed.ncbi.nlm.nih.gov/19118553
https://pubmed.ncbi.nlm.nih.gov/19118553
Publikováno v:
Clinical Neurophysiology. 125:S198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::372c2821e9f62129564c05df2c454e9a
https://doi.org/10.1016/s1388-2457(14)50648-7
https://doi.org/10.1016/s1388-2457(14)50648-7
Autor:
S. M. A. van der Salm, E.M.J. Foncke, M. Tijssen, J.H. Koelman, Lo J. Bour, A.F. van Rootselaar, J.C. Rothwell, K. Bhatia
Publikováno v:
Parkinsonism & Related Disorders. 13:S174
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17650b035c062a484a3fb94ee3136b32
https://doi.org/10.1016/s1353-8020(08)70882-4
https://doi.org/10.1016/s1353-8020(08)70882-4