These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
12. Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family. Spacey SD; Vanmolkot KR; Murphy C; van den Maagdenberg AM; Hsiung RG Headache; 2005 Oct; 45(9):1244-9. PubMed ID: 16178956 [TBL] [Abstract][Full Text] [Related]
13. [Genetics of migraine]. Ducros A Pathol Biol (Paris); 2000 Sep; 48(7):658-62. PubMed ID: 11072644 [TBL] [Abstract][Full Text] [Related]
14. The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility. D'Onofrio M; Ambrosini A; Di Mambro A; Arisi I; Santorelli FM; Grieco GS; Nicoletti F; Nappi G; Pierelli F; Schoenen J; Buzzi MG Neurosci Lett; 2009 Mar; 453(1):12-5. PubMed ID: 19429006 [TBL] [Abstract][Full Text] [Related]
15. 1H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1. Dichgans M; Herzog J; Freilinger T; Wilke M; Auer DP Neurology; 2005 Feb; 64(4):608-13. PubMed ID: 15728280 [TBL] [Abstract][Full Text] [Related]
17. Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus. Jones KW; Ehm MG; Pericak-Vance MA; Haines JL; Boyd PR; Peroutka SJ Genomics; 2001 Dec; 78(3):150-4. PubMed ID: 11735221 [TBL] [Abstract][Full Text] [Related]
18. [From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene]. Kors EE; Vanmolkot KR; Haan J; van den Maagdenberg AM; Frants RR; Ferrari MD Ned Tijdschr Geneeskd; 2004 Sep; 148(39):1919-20. PubMed ID: 15495990 [TBL] [Abstract][Full Text] [Related]
19. Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation. Malpas TJ; Riant F; Tournier-Lasserve E; Vahedi K; Neville BG Dev Med Child Neurol; 2010 Jan; 52(1):103-4. PubMed ID: 19811514 [No Abstract] [Full Text] [Related]
20. CACNA1A nonsense mutation is associated with basilar-type migraine and episodic ataxia type 2. Robbins MS; Lipton RB; Laureta EC; Grosberg BM Headache; 2009 Jul; 49(7):1042-6. PubMed ID: 19486177 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]