316 related articles for article (PubMed ID: 9403481)
21. Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine.
Dichgans M; Mayer M; Müller-Myhsok B; Straube A; Gasser T
Genomics; 1996 Feb; 32(1):151-4. PubMed ID: 8786108
[TBL] [Abstract][Full Text] [Related]
22. Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity.
Masotti C; Oliveira KG; Poerner F; Splendore A; Souza J; Freitas Rda S; Zechi-Ceide R; Guion-Almeida ML; Passos-Bueno MR
Eur J Hum Genet; 2008 Feb; 16(2):145-52. PubMed ID: 18000524
[TBL] [Abstract][Full Text] [Related]
23. Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Vanmolkot KR; Kors EE; Hottenga JJ; Terwindt GM; Haan J; Hoefnagels WA; Black DF; Sandkuijl LA; Frants RR; Ferrari MD; van den Maagdenberg AM
Ann Neurol; 2003 Sep; 54(3):360-6. PubMed ID: 12953268
[TBL] [Abstract][Full Text] [Related]
24. Genetic heterogeneity of familial hemiplegic migraine.
Joutel A; Ducros A; Vahedi K; Labauge P; Delrieu O; Pinsard N; Mancini J; Ponsot G; Gouttière F; Gastaut JL
Am J Hum Genet; 1994 Dec; 55(6):1166-72. PubMed ID: 7977376
[TBL] [Abstract][Full Text] [Related]
25. A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
Fernandez DM; Hand CK; Sweeney BJ; Parfrey NA
Headache; 2008 Jan; 48(1):101-8. PubMed ID: 18184292
[TBL] [Abstract][Full Text] [Related]
26. The molecular genetics of migraine.
Wessman M; Kaunisto MA; Kallela M; Palotie A
Ann Med; 2004; 36(6):462-73. PubMed ID: 15513297
[TBL] [Abstract][Full Text] [Related]
27. Association analysis of chromosome 1 migraine candidate genes.
Fernandez F; Curtain RP; Colson NJ; Ovcaric M; MacMillan J; Griffiths LR
BMC Med Genet; 2007 Aug; 8():57. PubMed ID: 17727731
[TBL] [Abstract][Full Text] [Related]
28. [Familial and sporadic hemiplegic migraine].
Ducros A
Rev Neurol (Paris); 2008 Mar; 164(3):216-24. PubMed ID: 18405771
[TBL] [Abstract][Full Text] [Related]
29. A novel locus for generalized epilepsy with febrile seizures plus in French families.
Baulac S; Gourfinkel-An I; Couarch P; Depienne C; Kaminska A; Dulac O; Baulac M; LeGuern E; Nabbout R
Arch Neurol; 2008 Jul; 65(7):943-51. PubMed ID: 18625863
[TBL] [Abstract][Full Text] [Related]
30. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
Ophoff RA; Terwindt GM; Vergouwe MN; van Eijk R; Oefner PJ; Hoffman SM; Lamerdin JE; Mohrenweiser HW; Bulman DE; Ferrari M; Haan J; Lindhout D; van Ommen GJ; Hofker MH; Ferrari MD; Frants RR
Cell; 1996 Nov; 87(3):543-52. PubMed ID: 8898206
[TBL] [Abstract][Full Text] [Related]
33. [Molecular genetic findings in migraine].
Østergaard E; Thomsen LL; Russell MB
Ugeskr Laeger; 2001 Nov; 163(45):6260-5. PubMed ID: 11723684
[TBL] [Abstract][Full Text] [Related]
34. Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.
Nyholt DR; Lea RA; Goadsby PJ; Brimage PJ; Griffiths LR
Neurology; 1998 May; 50(5):1428-32. PubMed ID: 9596000
[TBL] [Abstract][Full Text] [Related]
35. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
[TBL] [Abstract][Full Text] [Related]
36. The physiopathology of migraine: the contribution of genetics.
Montagna P
Neurol Sci; 2004 Oct; 25 Suppl 3():S93-6. PubMed ID: 15549578
[TBL] [Abstract][Full Text] [Related]
37. Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican families.
Huertas-Vázquez A; del Rincón JP; Canizales-Quinteros S; Riba L; Vega-Hernández G; Ramírez-Jiménez S; Aurón-Gómez M; Gómez-Pérez FJ; Aguilar-Salinas CA; Tusié-Luna MT
Ann Hum Genet; 2004 Sep; 68(Pt 5):419-27. PubMed ID: 15469419
[TBL] [Abstract][Full Text] [Related]
38. [Genetics of migraine].
Ducros A
Pathol Biol (Paris); 2000 Sep; 48(7):658-62. PubMed ID: 11072644
[TBL] [Abstract][Full Text] [Related]
39. Basilar-type migraine: clinical, epidemiologic, and genetic features.
Kirchmann M; Thomsen LL; Olesen J
Neurology; 2006 Mar; 66(6):880-6. PubMed ID: 16567706
[TBL] [Abstract][Full Text] [Related]
40. Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.
Terwindt GM; Ophoff RA; Haan J; Vergouwe MN; van Eijk R; Frants RR; Ferrari MD
Neurology; 1998 Apr; 50(4):1105-10. PubMed ID: 9566402
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
