330 related articles for article (PubMed ID: 9748855)
1. [Familial hemiplegic migraine].
Thomsen LL; Olesen J; Russell MB
Ugeskr Laeger; 1998 Sep; 160(37):5325-9. PubMed ID: 9748855
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Genetic heterogeneity of familial hemiplegic migraine.
Ophoff RA; van Eijk R; Sandkuijl LA; Terwindt GM; Grubben CP; Haan J; Lindhout D; Ferrari MD; Frants RR
Genomics; 1994 Jul; 22(1):21-6. PubMed ID: 7959770
[TBL] [Abstract][Full Text] [Related]
4. Familial hemiplegic migraine: involvement of a calcium neuronal channel.
Ophoff RA; Terwindt GM; Vergouwe MN; Frants RR; Ferrari MD
Neurologia; 1997 Dec; 12 Suppl 5():31-7. PubMed ID: 9436352
[TBL] [Abstract][Full Text] [Related]
5. The genetic spectrum of a population-based sample of familial hemiplegic migraine.
Thomsen LL; Kirchmann M; Bjornsson A; Stefansson H; Jensen RM; Fasquel AC; Petursson H; Stefansson M; Frigge ML; Kong A; Gulcher J; Stefansson K; Olesen J
Brain; 2007 Feb; 130(Pt 2):346-56. PubMed ID: 17142831
[TBL] [Abstract][Full Text] [Related]
6. [Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19].
Joutel A; Bousser MG; Biousse V; Labauge P; Chabriat H; Nibbio A; Maciazek J; Meyer B; Bach MA; Weissenbach J
Rev Neurol (Paris); 1994; 150(5):340-5. PubMed ID: 7878319
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [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]
9. Familial hemiplegic migraine, nystagmus, and cerebellar atrophy.
Elliott MA; Peroutka SJ; Welch S; May EF
Ann Neurol; 1996 Jan; 39(1):100-6. PubMed ID: 8572654
[TBL] [Abstract][Full Text] [Related]
10. Familial migraine: exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p.
Hovatta I; Kallela M; Färkkilä M; Peltonen L
Genomics; 1994 Oct; 23(3):707-9. PubMed ID: 7851903
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.
Vanmolkot KR; Kors EE; Turk U; Turkdogan D; Keyser A; Broos LA; Kia SK; van den Heuvel JJ; Black DF; Haan J; Frants RR; Barone V; Ferrari MD; Casari G; Koenderink JB; van den Maagdenberg AM
Eur J Hum Genet; 2006 May; 14(5):555-60. PubMed ID: 16538223
[TBL] [Abstract][Full Text] [Related]
13. A gene for familial hemiplegic migraine maps to chromosome 19.
Joutel A; Bousser MG; Biousse V; Labauge P; Chabriat H; Nibbio A; Maciazek J; Meyer B; Bach MA; Weissenbach J
Nat Genet; 1993 Sep; 5(1):40-5. PubMed ID: 8220421
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
Alonso I; Barros J; Tuna A; Coelho J; Sequeiros J; Silveira I; Coutinho P
Arch Neurol; 2003 Apr; 60(4):610-4. PubMed ID: 12707077
[TBL] [Abstract][Full Text] [Related]
16. Familial hemiplegic migraine in developmental age: report of two cases.
Lendvai D; Monteleone F; Melpignano G; Turri E; Verdecchia P; Cantani A
Riv Eur Sci Med Farmacol; 1996; 18(4):143-7. PubMed ID: 9177612
[TBL] [Abstract][Full Text] [Related]
17. Management of sporadic and familial hemiplegic migraine.
Russell MB
Expert Rev Neurother; 2010 Mar; 10(3):381-7. PubMed ID: 20187861
[TBL] [Abstract][Full Text] [Related]
18. Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group.
Terwindt GM; Ophoff RA; Haan J; Sandkuijl LA; Frants RR; Ferrari MD
Eur J Hum Genet; 1998; 6(4):297-307. PubMed ID: 9781035
[TBL] [Abstract][Full Text] [Related]
19. Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2.
Kors EE; Vanmolkot KR; Haan J; Kheradmand Kia S; Stroink H; Laan LA; Gill DS; Pascual J; van den Maagdenberg AM; Frants RR; Ferrari MD
Neuropediatrics; 2004 Oct; 35(5):293-6. PubMed ID: 15534763
[TBL] [Abstract][Full Text] [Related]
20. Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.
Jones KW; Ehm MG; Pericak-Vance MA; Haines JL; Boyd PR; Peroutka SJ
Genomics; 2001 Dec; 78(3):150-4. PubMed ID: 11735221
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]