van Kempen MJ - Search Results

1

Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome.

Volkers L, Kahlig KM, Verbeek NE, Das JH, van Kempen MJ, Stroink H, Augustijn P, van Nieuwenhuizen O, Lindhout D, George AL Jr, Koeleman BP, Rook MB. Volkers L, et al. Among authors: van kempen mj, van nieuwenhuizen o. Eur J Neurosci. 2011 Oct;34(8):1268-75. doi: 10.1111/j.1460-9568.2011.07826.x. Epub 2011 Aug 22. Eur J Neurosci. 2011. PMID: 21864321 Free PMC article.

2

Gap junctions in human umbilical cord endothelial cells contain multiple connexins.

Van Rijen H, van Kempen MJ, Analbers LJ, Rook MB, van Ginneken AC, Gros D, Jongsma HJ. Van Rijen H, et al. Among authors: van ginneken ac, van kempen mj. Am J Physiol. 1997 Jan;272(1 Pt 1):C117-30. doi: 10.1152/ajpcell.1997.272.1.C117. Am J Physiol. 1997. PMID: 9038818

3

Gap junctions in the rabbit sinoatrial node.

Verheule S, van Kempen MJ, Postma S, Rook MB, Jongsma HJ. Verheule S, et al. Among authors: van kempen mj. Am J Physiol Heart Circ Physiol. 2001 May;280(5):H2103-15. doi: 10.1152/ajpheart.2001.280.5.H2103. Am J Physiol Heart Circ Physiol. 2001. PMID: 11299212 Free article.

4

P19 embryonal carcinoma cells: a suitable model system for cardiac electrophysiological differentiation at the molecular and functional level.

van der Heyden MA, van Kempen MJ, Tsuji Y, Rook MB, Jongsma HJ, Opthof T. van der Heyden MA, et al. Among authors: van kempen mj. Cardiovasc Res. 2003 May 1;58(2):410-22. doi: 10.1016/s0008-6363(03)00247-5. Cardiovasc Res. 2003. PMID: 12757875

5

Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.

Volkers L, Rook MB, Das JH, Verbeek NE, Groenewegen WA, van Kempen MJ, Lindhout D, Koeleman BP. Volkers L, et al. Among authors: van kempen mj. Neurosci Lett. 2009 Oct 2;462(1):24-9. doi: 10.1016/j.neulet.2009.06.064. Epub 2009 Jun 25. Neurosci Lett. 2009. PMID: 19559753

6

Novel SCN1A mutations in Indonesian patients with severe myoclonic epilepsy in infancy.

Herini ES, Gunadi, van Kempen MJ, Yusoff S, Sutaryo, Sunartini, Patria SY, Matsuo M, Lindhout D, Nishio H. Herini ES, et al. Among authors: van kempen mj. Pediatr Int. 2010 Apr;52(2):234-9. doi: 10.1111/j.1442-200X.2009.02916.x. Epub 2009 Jun 26. Pediatr Int. 2010. PMID: 19563458

7

Adults with a history of possible Dravet syndrome: an illustration of the importance of analysis of the SCN1A gene.

Verbeek NE, van Kempen M, Gunning WB, Renier WO, Westland B, Lindhout D, Brilstra EH. Verbeek NE, et al. Epilepsia. 2011 Apr;52(4):e23-5. doi: 10.1111/j.1528-1167.2011.02982.x. Epub 2011 Mar 3. Epilepsia. 2011. PMID: 21371021 Free article. Review.

8

A retrospective population-based study on seizures related to childhood vaccination.

von Spiczak S, Helbig I, Drechsel-Baeuerle U, Muhle H, van Baalen A, van Kempen MJ, Lindhout D, Scheffer IE, Berkovic SF, Stephani U, Keller-Stanislawski B. von Spiczak S, et al. Among authors: van kempen mj, van baalen a. Epilepsia. 2011 Aug;52(8):1506-12. doi: 10.1111/j.1528-1167.2011.03134.x. Epub 2011 Jun 21. Epilepsia. 2011. PMID: 21692791 Free article.

9

Prevalence of SCN1A-related dravet syndrome among children reported with seizures following vaccination: a population-based ten-year cohort study.

Verbeek NE, van der Maas NA, Jansen FE, van Kempen MJ, Lindhout D, Brilstra EH. Verbeek NE, et al. Among authors: van der maas na, van kempen mj. PLoS One. 2013 Jun 6;8(6):e65758. doi: 10.1371/journal.pone.0065758. Print 2013. PLoS One. 2013. PMID: 23762420 Free PMC article.

10

Febrile temperatures unmask biophysical defects in Nav1.1 epilepsy mutations supportive of seizure initiation.

Volkers L, Kahlig KM, Das JH, van Kempen MJ, Lindhout D, Koeleman BP, Rook MB. Volkers L, et al. Among authors: van kempen mj. J Gen Physiol. 2013 Dec;142(6):641-53. doi: 10.1085/jgp.201311042. J Gen Physiol. 2013. PMID: 24277604 Free PMC article.

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