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3. Genetic heterogeneity in Italian families with familial hemiplegic migraine. Carrera P; Piatti M; Stenirri S; Grimaldi LM; Marchioni E; Curcio M; Righetti PG; Ferrari M; Gelfi C Neurology; 1999 Jul; 53(1):26-33. PubMed ID: 10408532 [TBL] [Abstract][Full Text] [Related]
8. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity. Ducros A; Joutel A; Vahedi K; Cecillon M; Ferreira A; Bernard E; Verier A; Echenne B; Lopez de Munain A; Bousser MG; Tournier-Lasserve E Ann Neurol; 1997 Dec; 42(6):885-90. PubMed ID: 9403481 [TBL] [Abstract][Full Text] [Related]
9. Families linked and unlinked to chromosome 19 with familial hemiplegic migraine. Peroutka SJ Cephalalgia; 1996 May; 16(3):138. PubMed ID: 8734764 [No Abstract] [Full Text] [Related]
10. Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine. Kors EE; Haan J; Giffin NJ; Pazdera L; Schnittger C; Lennox GG; Terwindt GM; Vermeulen FL; Van den Maagdenberg AM; Frants RR; Ferrari MD Arch Neurol; 2003 May; 60(5):684-8. PubMed ID: 12756131 [TBL] [Abstract][Full Text] [Related]
16. Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group. Haan J; Terwindt GM; Bos PL; Ophoff RA; Frants RR; Ferrari MD Clin Neurol Neurosurg; 1994 Aug; 96(3):244-9. PubMed ID: 7988094 [TBL] [Abstract][Full Text] [Related]
17. A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group. Ophoff RA; Terwindt GM; Vergouwe MN; van Eijk R; Mohrenweiser H; Litt M; Hofker MH; Haan J; Ferrari MD; Frants RR Eur J Hum Genet; 1996; 4(6):321-8. PubMed ID: 9043864 [TBL] [Abstract][Full Text] [Related]