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Page 1
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Heinzen EL, Swoboda KJ, Hitomi Y, Gurrieri F, Nicole S, de Vries B, Tiziano FD, Fontaine B, Walley NM, Heavin S, Panagiotakaki E; European Alternating Hemiplegia of Childhood (AHC) Genetics Consortium; Biobanca e Registro Clinico per l'Emiplegia Alternante (I.B.AHC) Consortium; European Network for Research on Alternating Hemiplegia (ENRAH) for Small and Medium-sized Enterpriese (SMEs) Consortium; Fiori S, Abiusi E, Di Pietro L, Sweney MT, Newcomb TM, Viollet L, Huff C, Jorde LB, Reyna SP, Murphy KJ, Shianna KV, Gumbs CE, Little L, Silver K, Ptáček LJ, Haan J, Ferrari MD, Bye AM, Herkes GK, Whitelaw CM, Webb D, Lynch BJ, Uldall P, King MD, Scheffer IE, Neri G, Arzimanoglou A, van den Maagdenberg AM, Sisodiya SM, Mikati MA, Goldstein DB. Heinzen EL, et al. Among authors: van den maagdenberg am. Nat Genet. 2012 Sep;44(9):1030-4. doi: 10.1038/ng.2358. Epub 2012 Jul 29. Nat Genet. 2012. PMID: 22842232 Free PMC article.
Mutant P/Q-type calcium channel electrophysiology and migraine.
Plomp JJ, van den Maagdenberg AM, Molenaar PC, Frants RR, Ferrari MD. Plomp JJ, et al. Among authors: van den maagdenberg am. Curr Opin Investig Drugs. 2001 Sep;2(9):1250-60. Curr Opin Investig Drugs. 2001. PMID: 11717812 Review.
Calcium channel mutations and migraine.
Kors EE, van den Maagdenberg AM, Plomp JJ, Frants RR, Ferrari MD. Kors EE, et al. Among authors: van den maagdenberg am. Curr Opin Neurol. 2002 Jun;15(3):311-6. doi: 10.1097/00019052-200206000-00014. Curr Opin Neurol. 2002. PMID: 12045730 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: van den maagdenberg am. 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.
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: van den maagdenberg am. 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: van den maagdenberg am. 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.
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.
Vanmolkot KR, Kors EE, Turk U, Turkdogan D, Keyser A, Broos LA, Kia SK, van den Heuvel JJ, Black DF, Haan J, Frants RR, Barone V, Ferrari MD, Casari G, Koenderink JB, van den Maagdenberg AM. Vanmolkot KR, et al. Among authors: van den maagdenberg am, van den heuvel jj. Eur J Hum Genet. 2006 May;14(5):555-60. doi: 10.1038/sj.ejhg.5201607. Eur J Hum Genet. 2006. PMID: 16538223
Genetic biomarkers for migraine.
De Vries B, Haan J, Frants RR, Van den Maagdenberg AM, Ferrari MD. De Vries B, et al. Among authors: van den maagdenberg am. Headache. 2006 Jul-Aug;46(7):1059-68. doi: 10.1111/j.1526-4610.2006.00499.x. Headache. 2006. PMID: 16866710 Review.
331 results