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.
44. 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]
48. A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine. Alonso I; Barros J; Tuna A; Seixas A; Coutinho P; Sequeiros J; Silveira I Clin Genet; 2004 Jan; 65(1):70-2. PubMed ID: 15032980 [No Abstract] [Full Text] [Related]
49. Imaging abnormalities in sporadic hemiplegic migraine on conventional MRI, diffusion and perfusion MRI and MRS. Jacob A; Mahavish K; Bowden A; Smith ET; Enevoldson P; White RP Cephalalgia; 2006 Aug; 26(8):1004-9. PubMed ID: 16886937 [TBL] [Abstract][Full Text] [Related]
50. [Familial hemiplegic migraine resulting in recurrent coma]. Lee H; Aramideh M; Ginjaar HB Ned Tijdschr Geneeskd; 2008 Feb; 152(7):393-6. PubMed ID: 18380388 [TBL] [Abstract][Full Text] [Related]
58. Familial hemiplegic migraine: EEG and CT scan study of two cases. Gastaut JL; Yermenos E; Bonnefoy M; Cros D Ann Neurol; 1981 Oct; 10(4):392-5. PubMed ID: 7316492 [TBL] [Abstract][Full Text] [Related]
59. Multimodal imaging of striatal degeneration in Amish patients with glutaryl-CoA dehydrogenase deficiency. Strauss KA; Lazovic J; Wintermark M; Morton DH Brain; 2007 Jul; 130(Pt 7):1905-20. PubMed ID: 17478444 [TBL] [Abstract][Full Text] [Related]
60. [Role of P/Q calcium channel in familial hemiplegic migraine]. Weiss N; Tournier-Lasserve E; De Waard M Med Sci (Paris); 2007 Jan; 23(1):53-63. PubMed ID: 17212932 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]