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2. [Phenotypic manifestations and genetic features of migraine]. Godinova AM Zh Nevropatol Psikhiatr Im S S Korsakova; 1967; 67(7):1002-7. PubMed ID: 5598776 [No Abstract] [Full Text] [Related]
3. Migraine: sex-influenced trait model? Wang XP; Liu JM; Zhao YB Med Hypotheses; 2008; 71(1):14-21. PubMed ID: 18289799 [TBL] [Abstract][Full Text] [Related]
4. [Developing conditions of migraine]. Soyka D Dtsch Med Wochenschr; 1978 Aug; 103(34):1342-5. PubMed ID: 354915 [No Abstract] [Full Text] [Related]
5. 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]
10. [Relationships between genotype and phenotype in Charcot-Marie-Tooth disease]. Câmpeanu E; Morariu M Rev Roum Neurol; 1970; 7(1):47-56. PubMed ID: 5527990 [No Abstract] [Full Text] [Related]
11. Evidence of shared genetic risk factors for migraine and rolandic epilepsy. Clarke T; Baskurt Z; Strug LJ; Pal DK Epilepsia; 2009 Nov; 50(11):2428-33. PubMed ID: 19674062 [TBL] [Abstract][Full Text] [Related]
12. [Complicated migraine in children (author's transl)]. Ritz A; Jacobi G; Emrich R Monatsschr Kinderheilkd; 1981 Sep; 129(9):504-12. PubMed ID: 7343827 [TBL] [Abstract][Full Text] [Related]
13. Testing models for genetic determination in migraine. Mochi M; Sangiorgi S; Cortelli P; Carelli V; Scapoli C; Crisci M; Monari L; Pierangeli G; Montagna P Cephalalgia; 1993 Dec; 13(6):389-94. PubMed ID: 8313452 [TBL] [Abstract][Full Text] [Related]
14. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. Lee H; Jen JC; Wang H; Chen Z; Mamsa H; Sabatti C; Baloh RW; Nelson SF Hum Mol Genet; 2006 Jan; 15(2):251-8. PubMed ID: 16330481 [TBL] [Abstract][Full Text] [Related]
15. Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms. Singh R; Macdonell RA; Scheffer IE; Crossland KM; Berkovic SF Epileptic Disord; 1999 Jun; 1(2):93-9. PubMed ID: 10937138 [TBL] [Abstract][Full Text] [Related]
16. Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL). Hutchinson M; O'Riordan J; Javed M; Quin E; Macerlaine D; Wilcox T; Parfrey N; Nagy TG; Tournier-Lasserve E Ann Neurol; 1995 Nov; 38(5):817-24. PubMed ID: 7486874 [TBL] [Abstract][Full Text] [Related]
17. Aetiology of migraine and prevention with carbamazepine (Tegretol): results of a double-blind, cross-over study. Rompel H; Bauermeister PW S Afr Med J; 1970 Jan; 44(4):75-80. PubMed ID: 4905910 [No Abstract] [Full Text] [Related]
18. [Epilepsy and migraine]. Badalian LO; Gorlina IS Klin Med (Mosk); 1969 Sep; 47(9):18-54. PubMed ID: 5397881 [No Abstract] [Full Text] [Related]
19. Genetic analysis of the inheritance of otosclerosis. Gapanavichyus BM; Venslauskas MI Sov Genet; 1974 Apr; 8(2):251-60. PubMed ID: 4846192 [No Abstract] [Full Text] [Related]
20. Sex differences in the transmission of migraine. Low NC; Cui L; Merikangas KR Cephalalgia; 2007 Aug; 27(8):935-42. PubMed ID: 17661867 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]