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PubPharm (107)
61
Observation of Autoregulation Indices During Ventricular CSF Drainage After Aneurysmal Subarachnoid Hemorrhage: A Pilot Study
enthalten in:
Neurocritical care
| 2015
von
Aries, M.
|
de Jong, S.
|
van Dijk, J.
| +5
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62
Cortical Myoclonus in a Young Boy with GOSR2 Mutation Mimics Chorea
enthalten in:
Movement disorders clinical practice
| 2015
von
van Egmond, M.
|
Kuiper, A.
|
Elting, J.
| +3
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63
Myoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment
enthalten in:
European journal of paediatric neurology
| 2015
von
van Egmond, M.
|
Elting, J.
|
Kuiper, A.
| +7
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64
Letter by Aries et al Regarding Article, "Optical Bedside Monitoring of Cerebral Blood Flow in Acute Ischemic Stroke Patients During Head-of-Bed Manipulation"
enthalten in:
Stroke
| 2014
von
Aries, M.
|
Vroomen, P.
|
Elting, J.
CommentOn: Stroke. 2014 May;45(5):1269-74. - PMID 24652308
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65
Reticular Myoclonus : It Really Comes From the Brainstem!
enthalten in:
Movement disorders clinical practice
| 2014
von
Beudel, M.
|
Elting, J.
|
Uyttenboogaart, M.
| +2
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66
Modulation of cerebral blood flow with transcutaneous electrical neurostimulation (TENS) in patients with cerebral vasospasm after subarachnoid hemorrhage
enthalten in:
Neuromodulation : journal of the International Neuromodulation Society
| 2014
von
ter Laan, M.
|
van Dijk, J.
|
Stewart, R.
| +2
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67
Modulation of Cerebral Blood Flow With Transcutaneous Electrical Neurostimulation (TENS) in Patients With Cerebral Vasospasm After Subarachnoid Hemorrhage
enthalten in:
Neuromodulation
| 2014
von
Laan, M.
|
Dijk, J.
|
Stewart, R.
| +2
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68
Facial tics and spasms
enthalten in:
Nederlands tijdschrift voor geneeskunde
| 2014
von
Potgieser, A.
|
van Dijk, J.
|
Elting, J.
| +1
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69
Ramsay Hunt syndrome : clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2014
von
van Egmond, M.
|
Verschuuren-Bemelmans, C.
|
Nibbeling, E.
| +8
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70
Ramsay hunt syndrome: Clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation
enthalten in:
Movement disorders
| 2014
von
Egmond, M.
|
Verschuuren‐Bemelmans, C.
|
Nibbeling, E.
| +8
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myoclonus
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