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Journal Abstract Search
328 related items for PubMed ID: 18451712
1. Genetics of migraine: an update with special attention to genetic comorbidity. Stam AH, van den Maagdenberg AM, Haan J, Terwindt GM, Ferrari MD. Curr Opin Neurol; 2008 Jun; 21(3):288-93. PubMed ID: 18451712 [Abstract] [Full Text] [Related]
2. FHM3 in familial hemiplegic migraine is more resistant to mutation than FHM1 and FHM2. Wiwanitkit V. J Neurol Sci; 2009 Feb 15; 277(1-2):76-9. PubMed ID: 19007941 [Abstract] [Full Text] [Related]
8. The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online. Vanmolkot KR, Babini E, de Vries B, Stam AH, Freilinger T, Terwindt GM, Norris L, Haan J, Frants RR, Ramadan NM, Ferrari MD, Pusch M, van den Maagdenberg AM, Dichgans M. Hum Mutat; 2007 May 15; 28(5):522. PubMed ID: 17397047 [Abstract] [Full Text] [Related]
9. Two novel SCN1A mutations identified in families with familial hemiplegic migraine. Weller CM, Pelzer N, de Vries B, López MA, De Fàbregues O, Pascual J, Arroyo MA, Koelewijn SC, Stam AH, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AM. Cephalalgia; 2014 Nov 15; 34(13):1062-9. PubMed ID: 24707016 [Abstract] [Full Text] [Related]
18. Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4. von Brevern M, Ta N, Shankar A, Wiste A, Siegel A, Radtke A, Sander T, Escayg A. Headache; 2006 May 15; 46(7):1136-41. PubMed ID: 16866717 [Abstract] [Full Text] [Related]
20. Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes. Cuenca-León E, Corominas R, Fernàndez-Castillo N, Volpini V, Del Toro M, Roig M, Macaya A, Cormand B. Cephalalgia; 2008 Oct 15; 28(10):1039-47. PubMed ID: 18644040 [Abstract] [Full Text] [Related] Page: [Next] [New Search]