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12. CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood. de Vries B; Stam AH; Beker F; van den Maagdenberg AM; Vanmolkot KR; Laan L; Ginjaar IB; Frants RR; Lauffer H; Haan J; Haas JP; Terwindt GM; Ferrari MD Cephalalgia; 2008 Aug; 28(8):887-91. PubMed ID: 18498393 [TBL] [Abstract][Full Text] [Related]
13. Clinical aspects of familial hemiplegic migraine in two families. O'Hare JA; Feely MJ; Callaghan N Ir Med J; 1981 Oct; 74(10):291-5. PubMed ID: 7309446 [No Abstract] [Full Text] [Related]
14. Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene. Haan J; Kors EE; Terwindt GM; Vermeulen FL; Vergouwe MN; van den Maagdenberg AM; Gill DS; Pascual J; Ophoff RA; Frants RR; Ferrari Cephalalgia; 2000 Oct; 20(8):696-700. PubMed ID: 11167897 [TBL] [Abstract][Full Text] [Related]
15. Reversible cerebellar perfusion in familial hemiplegic migraine. Lee TG; Solomon GD; Kunkel RS; Raja S Lancet; 1996 Nov; 348(9038):1383. PubMed ID: 8918294 [No Abstract] [Full Text] [Related]
17. Paroxysmal disorders associated with PRRT2 mutations shake up expectations on ion channel genes. Guerrini R; Mink JW Neurology; 2012 Nov; 79(21):2086-8. PubMed ID: 23077020 [No Abstract] [Full Text] [Related]
18. 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]
19. Cerebral angiography complications link cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy to familial hemiplegic migraine. Weller M; Petersen D; Dichgans J; Klockgether T Neurology; 1996 Mar; 46(3):844. PubMed ID: 8618700 [No Abstract] [Full Text] [Related]
20. From genetics to prophylaxis. Ferrari M Cephalalgia; 1997 Jun; 17 Suppl 17():2-4; discussion 4-5. PubMed ID: 9218877 [No Abstract] [Full Text] [Related] [Next] [New Search]