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of 149
pro vyhledávání: '"van der Hoeven, J.H."'
Publikováno v:
In Clinical Neurophysiology January 2017 128(1):253-259
Autor:
van der Stouwe, A.M.M., Elting, J.W., van der Hoeven, J.H., van Laar, T., Leenders, K.L., Maurits, N.M., Tijssen, M.A.J.
Publikováno v:
In Parkinsonism and Related Disorders September 2016 30:23-28
Reproducibility and variability of dynamic cerebral autoregulation during passive cyclic leg raising
Publikováno v:
In Medical Engineering and Physics May 2014 36(5):585-591
Publikováno v:
In Parkinsonism and Related Disorders 2009 15(8):564-571
Autor:
van de Wassenberg, W.J.G., Kruizinga, W.J., van der Hoeven, J.H., Leenders, K.L., Maurits, N.M.
Publikováno v:
In Neurophysiologie Clinique / Clinical Neurophysiology 2008 38(5):277-288
Publikováno v:
In Clinical Neurophysiology 2008 119(6):1379-1384
Autor:
Bok, L.A., Halbertsma, F.J., Houterman, S., Wevers, R.A., Vreeswijk, C.M.J.M., Jakobs, C., Struys, E., van der Hoeven, J.H., Sival, D.A., Willemsen, M.A.
Publikováno v:
Developmental Medicine & Child Neurology, 54, 9, pp. 849-854
Developmental Medicine & Child Neurology, 54, 849-854
Developmental Medicine and Child Neurology, 54(9), 849-854. Wiley-Blackwell
Bok, L A, Halbertsma, F J, Houterman, S, Wevers, R A, Vreeswijk, C, Jakobs, C A J M, Struijs, E A, van der Hoeven, J H, Sival, D A & Willemsen, M A 2012, ' Long-term outcome in pyridoxine-dependent epilepsy ', Developmental Medicine and Child Neurology, vol. 54, no. 9, pp. 849-854 . https://doi.org/10.1111/j.1469-8749.2012.04347.x
Developmental Medicine & Child Neurology, 54, 849-854
Developmental Medicine and Child Neurology, 54(9), 849-854. Wiley-Blackwell
Bok, L A, Halbertsma, F J, Houterman, S, Wevers, R A, Vreeswijk, C, Jakobs, C A J M, Struijs, E A, van der Hoeven, J H, Sival, D A & Willemsen, M A 2012, ' Long-term outcome in pyridoxine-dependent epilepsy ', Developmental Medicine and Child Neurology, vol. 54, no. 9, pp. 849-854 . https://doi.org/10.1111/j.1469-8749.2012.04347.x
Item does not contain fulltext Aim The long-term outcome of the Dutch pyridoxine-dependent epilepsy cohort and correlations between patient characteristics and follow-up data were retrospectively studied. Method Fourteen patients recruited from a nat
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Acute trismus can have different causes. We describe the presentation, course and radiological findings of a 34-year-old man who developed acute trismus and MRI findings consistent with the combination of an old and fresh infarction in the genu of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::a9a000f81c0790e5bf4b467564643ec7
https://hdl.handle.net/20.500.14017/76ef2c6e-a61d-402f-b765-38b2ba52ae93
https://hdl.handle.net/20.500.14017/76ef2c6e-a61d-402f-b765-38b2ba52ae93
Publikováno v:
Nederlands Tijdschrift voor Geneeskunde, 148(21), 1035-1038. NLM (Medline)
Hypokalaemic periodic paralysis is an autosomal, dominantly inherited disorder, characterised by attacks of partial or total muscle weakness and serum hypokalaemia. The mutations responsible are located in the CACNA1S gene (type 1) and in the SCN4A g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::e9ad8da0e74595b0179511b41cc51f28
https://research.rug.nl/en/publications/3958690c-82f0-4c3d-9dfd-a6d7558629e0
https://research.rug.nl/en/publications/3958690c-82f0-4c3d-9dfd-a6d7558629e0