180 related articles for article (PubMed ID: 24286483)
1. Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci.
Addis L; Chiang T; Clarke T; Hardison H; Kugler S; Mandelbaum DE; Novotny E; Wolf S; Strug LJ; Pal DK
Genes Brain Behav; 2014 Mar; 13(3):333-40. PubMed ID: 24286483
[TBL] [Abstract][Full Text] [Related]
2. The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.
Strug LJ; Addis L; Chiang T; Baskurt Z; Li W; Clarke T; Hardison H; Kugler SL; Mandelbaum DE; Novotny EJ; Wolf SM; Pal DK
PLoS One; 2012; 7(7):e40696. PubMed ID: 22815793
[TBL] [Abstract][Full Text] [Related]
3. Pleiotropic effects of the 11p13 locus on developmental verbal dyspraxia and EEG centrotemporal sharp waves.
Pal DK; Li W; Clarke T; Lieberman P; Strug LJ
Genes Brain Behav; 2010 Nov; 9(8):1004-12. PubMed ID: 20825490
[TBL] [Abstract][Full Text] [Related]
4. Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees.
Curtain RP; Lea RA; Tajouri L; Haupt LM; Ovcaric M; MacMillan J; Griffiths LR
Neurol Res; 2005 Sep; 27(6):647-52. PubMed ID: 16157018
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs.
Spadaro M; Ursu S; Lehmann-Horn F; Veneziano L; Antonini G; Giunti P; Frontali M; Jurkat-Rott K
Neurogenetics; 2004 Sep; 5(3):177-85. PubMed ID: 15459825
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locus.
Thompson MD; Noble-Topham S; Percy ME; Andrade DM; Ebers GC
Neuroreport; 2012 Jan; 23(1):45-8. PubMed ID: 22107845
[TBL] [Abstract][Full Text] [Related]
10. Significant linkage to migraine with aura on chromosome 11q24.
Cader ZM; Noble-Topham S; Dyment DA; Cherny SS; Brown JD; Rice GP; Ebers GC
Hum Mol Genet; 2003 Oct; 12(19):2511-7. PubMed ID: 12915447
[TBL] [Abstract][Full Text] [Related]
11. Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.
Marconi R; De Fusco M; Aridon P; Plewnia K; Rossi M; Carapelli S; Ballabio A; Morgante L; Musolino R; Epifanio A; Micieli G; De Michele G; Casari G
Ann Neurol; 2003 Mar; 53(3):376-81. PubMed ID: 12601705
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Genetics of migraine: an update with special attention to genetic comorbidity.
Stam AH; van den Maagdenberg AM; Haan J; Terwindt GM; Ferrari MD
Curr Opin Neurol; 2008 Jun; 21(3):288-93. PubMed ID: 18451712
[TBL] [Abstract][Full Text] [Related]
14. Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.
Roth C; Freilinger T; Kirovski G; Dunkel J; Shah Y; Wilken B; Rautenstrauß B; Ferbert A
Cephalalgia; 2014 Mar; 34(3):183-90. PubMed ID: 24096472
[TBL] [Abstract][Full Text] [Related]
15. Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.
Cevoli S; Pierangeli G; Monari L; Valentino ML; Bernardoni P; Mochi M; Cortelli P; Montagna P
Neurol Sci; 2002 Apr; 23(1):7-10. PubMed ID: 12111614
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.
Neubauer BA; Fiedler B; Himmelein B; Kämpfer F; Lässker U; Schwabe G; Spanier I; Tams D; Bretscher C; Moldenhauer K; Kurlemann G; Weise S; Tedroff K; Eeg-Olofsson O; Wadelius C; Stephani U
Neurology; 1998 Dec; 51(6):1608-12. PubMed ID: 9855510
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
