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Year Number of Results
1991 1
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1999 2
2000 3
2001 5
2002 1
2003 1
2004 3
2005 2
2006 1
2008 1
2009 4
2010 2
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2016 3
2017 1
2018 3
2019 2
2020 1
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52 results

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Page 1
Heart defects in connexin43-deficient mice.
Ya J, Erdtsieck-Ernste EB, de Boer PA, van Kempen MJ, Jongsma H, Gros D, Moorman AF, Lamers WH. Ya J, et al. Among authors: van kempen mj. Circ Res. 1998 Feb 23;82(3):360-6. doi: 10.1161/01.res.82.3.360. Circ Res. 1998. PMID: 9486664 Review.
Modifier genes in SCN1A-related epilepsy syndromes.
de Lange IM, Mulder F, van 't Slot R, Sonsma ACM, van Kempen MJA, Nijman IJ, Ernst RF, Knoers NVAM, Brilstra EH, Koeleman BPC. de Lange IM, et al. Among authors: van kempen mja. Mol Genet Genomic Med. 2020 Apr;8(4):e1103. doi: 10.1002/mgg3.1103. Epub 2020 Feb 7. Mol Genet Genomic Med. 2020. PMID: 32032478 Free PMC article.
The immune response in adenoids and tonsils.
van Kempen MJ, Rijkers GT, Van Cauwenberge PB. van Kempen MJ, et al. Int Arch Allergy Immunol. 2000 May;122(1):8-19. doi: 10.1159/000024354. Int Arch Allergy Immunol. 2000. PMID: 10859465 Review.
Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome.
Buijsse N, Jansen FE, Ockeloen CW, van Kempen MJA, Zeidler S, Willemsen MH, Scarano E, Monticone S, Zonneveld-Huijssoon E, Low KJ, Bayat A, Sisodiya SM, Samanta D, Lesca G, de Jong D, Giltay JC, Verbeek NE, Kleefstra T, Brilstra EH, Vlaskamp DRM. Buijsse N, et al. Among authors: van kempen mja. Epilepsia Open. 2023 Dec;8(4):1300-1313. doi: 10.1002/epi4.12799. Epub 2023 Aug 18. Epilepsia Open. 2023. PMID: 37501353 Free PMC article.
Viral rhinitis and asthma.
Van Cauwenberge PB, Vermeiren JS, van Kempen MJ. Van Cauwenberge PB, et al. Among authors: van kempen mj. Curr Opin Allergy Clin Immunol. 2001 Feb;1(1):21-5. doi: 10.1097/01.all.0000010980.24867.24. Curr Opin Allergy Clin Immunol. 2001. PMID: 11964665 Review.
The common cold.
Van Cauwenberge PB, van Kempen MJ, Bachert C. Van Cauwenberge PB, et al. Among authors: van kempen mj. Acta Otorhinolaryngol Belg. 2000;54(3):397-401. Acta Otorhinolaryngol Belg. 2000. PMID: 11082776
Congenital epulis of the jaw: a series of five cases and review of literature.
Küpers AM, Andriessen P, van Kempen MJ, van der Tol IG, Baart JA, Dumans AG, van der Waal I. Küpers AM, et al. Among authors: van kempen mj. Pediatr Surg Int. 2009 Feb;25(2):207-10. doi: 10.1007/s00383-008-2304-8. Epub 2008 Dec 12. Pediatr Surg Int. 2009. PMID: 19082830 Review.
Influence of common SCN1A promoter variants on the severity of SCN1A-related phenotypes.
de Lange IM, Weuring W, van 't Slot R, Gunning B, Sonsma ACM, McCormack M, de Kovel C, van Gemert LJJM, Mulder F, van Kempen MJA, Knoers NVAM, Brilstra EH, Koeleman BPC. de Lange IM, et al. Among authors: van kempen mja. Mol Genet Genomic Med. 2019 Jul;7(7):e00727. doi: 10.1002/mgg3.727. Epub 2019 May 29. Mol Genet Genomic Med. 2019. PMID: 31144463 Free PMC article.
Mutations in KCNT1 cause a spectrum of focal epilepsies.
Møller RS, Heron SE, Larsen LH, Lim CX, Ricos MG, Bayly MA, van Kempen MJ, Klinkenberg S, Andrews I, Kelley K, Ronen GM, Callen D, McMahon JM, Yendle SC, Carvill GL, Mefford HC, Nabbout R, Poduri A, Striano P, Baglietto MG, Zara F, Smith NJ, Pridmore C, Gardella E, Nikanorova M, Dahl HA, Gellert P, Scheffer IE, Gunning B, Kragh-Olsen B, Dibbens LM. Møller RS, et al. Among authors: van kempen mj. Epilepsia. 2015 Sep;56(9):e114-20. doi: 10.1111/epi.13071. Epub 2015 Jun 30. Epilepsia. 2015. PMID: 26122718 Free PMC article.
52 results