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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 2
2002 2
2003 2
2004 6
2005 3
2006 4
2007 7
2008 4
2009 3
2010 1
2023 0

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33 results

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Page 1
Recent findings in headache genetics.
Kors EE, Vanmolkot KR, Haan J, Frants RR, van den Maagdenberg AM, Ferrari MD. Kors EE, et al. Among authors: vanmolkot kr. Curr Opin Neurol. 2004 Jun;17(3):283-8. doi: 10.1097/00019052-200406000-00008. Curr Opin Neurol. 2004. PMID: 15167062 Review.
Migraine genetics: an update.
Haan J, Kors EE, Vanmolkot KR, van den Maagdenberg AM, Frants RR, Ferrari MD. Haan J, et al. Among authors: vanmolkot kr. Curr Pain Headache Rep. 2005 Jun;9(3):213-20. doi: 10.1007/s11916-005-0065-9. Curr Pain Headache Rep. 2005. PMID: 15907261 Review.
Toward a molecular genetic classification of familial hemiplegic migraine.
Haan J, Kors EE, van den Maagdenberg AM, Vanmolkot KR, Terwindt GM, Frants RR, Ferrari MD. Haan J, et al. Among authors: vanmolkot kr. Curr Pain Headache Rep. 2004 Jun;8(3):238-43. doi: 10.1007/s11916-004-0058-0. Curr Pain Headache Rep. 2004. PMID: 15115644 Review.
CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.
Stam AH, Vanmolkot KR, Kremer HP, Gärtner J, Brown J, Leshinsky-Silver E, Gilad R, Kors EE, Frankhuizen WS, Ginjaar HB, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM, Terwindt GM. Stam AH, et al. Among authors: vanmolkot kr. Clin Genet. 2008 Nov;74(5):481-5. doi: 10.1111/j.1399-0004.2008.00996.x. Epub 2008 Apr 8. Clin Genet. 2008. PMID: 18400034
Shared genetic factors in migraine and depression: evidence from a genetic isolate.
Stam AH, de Vries B, Janssens AC, Vanmolkot KR, Aulchenko YS, Henneman P, Oostra BA, Frants RR, van den Maagdenberg AM, Ferrari MD, van Duijn CM, Terwindt GM. Stam AH, et al. Among authors: vanmolkot kr. Neurology. 2010 Jan 26;74(4):288-94. doi: 10.1212/WNL.0b013e3181cbcd19. Epub 2010 Jan 13. Neurology. 2010. PMID: 20071666 Free PMC article.
Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM families.
Lopes LR, Peres MF, Vanmolkot KR, Tobo PR, Zukerman E, Frants RR, van den Maagdenberg AM, Moreira-Filho CA. Lopes LR, et al. Among authors: vanmolkot kr. Arq Neuropsiquiatr. 2006 Sep;64(3A):549-52. doi: 10.1590/s0004-282x2006000400001. Arq Neuropsiquiatr. 2006. PMID: 17119788 Free article.
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.
Castro MJ, Stam AH, Lemos C, Barros J, Gouveia RG, Martins IP, Koenderink JB, Vanmolkot KRJ, Mendes AP, Frants RR, Ferrari MD, Sequeiros J, Pereira-Monteiro JM, van den Maagdenberg AMJM. Castro MJ, et al. Among authors: vanmolkot krj. J Hum Genet. 2007;52(12):990-998. doi: 10.1007/s10038-007-0205-7. Epub 2007 Oct 19. J Hum Genet. 2007. PMID: 17952365
33 results