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Results: 16

1.

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 29;8:57.

2.

Minor head trauma-induced sporadic hemiplegic migraine coma.

Curtain RP, Smith RL, Ovcaric M, Griffiths LR.

Pediatr Neurol. 2006 Apr;34(4):329-32.

PMID:
16638514
3.

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.

PMID:
16157018
4.

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine.

Lea RA, Nyholt DR, Curtain RP, Ovcaric M, Sciascia R, Bellis C, Macmillan J, Quinlan S, Gibson RA, McCarthy LC, Riley JH, Smithies YJ, Kinrade S, Griffiths LR.

Neurogenetics. 2005 May;6(2):67-72. Epub 2005 Apr 14.

PMID:
15830246
5.

Investigation of an inducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population.

Tajouri L, Martin V, Ovcaric M, Curtain RP, Lea RA, Csurhes P, Pender MP, Griffiths LR.

Brain Res Bull. 2004 Jul 30;64(1):9-13.

PMID:
15275951
6.

An investigation of the 5-HT2C receptor gene as a migraine candidate gene.

Johnson MP, Lea RA, Curtain RP, MacMillan JC, Griffiths LR.

Am J Med Genet B Neuropsychiatr Genet. 2003 Feb;117B(1):86-9.

PMID:
12555241
7.

A typical migraine susceptibility region localizes to chromosome 1q31.

Lea RA, Shepherd AG, Curtain RP, Nyholt DR, Quinlan S, Brimage PJ, Griffiths LR.

Neurogenetics. 2002 Mar;4(1):17-22.

PMID:
12030327
8.

Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility.

Lea RA, Curtain RP, Hutchins C, Brimage PJ, Griffiths LR.

Am J Med Genet. 2001 Dec 8;105(8):707-12.

PMID:
11803518
9.

Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension.

Rutherford S, Johnson MP, Curtain RP, Griffiths LR.

Hum Genet. 2001 Oct;109(4):408-15.

PMID:
11702222
10.

No evidence for involvement of the human inducible nitric oxide synthase (iNOS) gene in susceptibility to typical migraine.

Lea RA, Curtain RP, Shepherd AG, Brimage PJ, Griffiths LR.

Am J Med Genet. 2001 Jan 8;105(1):110-3.

PMID:
11424980
11.

Familial typical migraine: significant linkage and localization of a gene to Xq24-28.

Nyholt DR, Curtain RP, Griffiths LR.

Hum Genet. 2000 Jul;107(1):18-23.

PMID:
10982029
12.

Influence of family history on frequency of glucagon receptor Gly40Ser mutation in hypertensive subjects.

Morris BJ, Jeyasingam CL, Zhang W, Curtain RP, Griffiths LR.

Hypertension. 1997 Dec;30(6):1640-1. No abstract available.

13.

Association of a low density lipoprotein receptor microsatellite variant with obesity.

Rutherford S, Nyholt DR, Curtain RP, Quinlan SR, Gaffney PT, Morris BJ, Griffiths LR.

Int J Obes Relat Metab Disord. 1997 Nov;21(11):1032-7.

PMID:
9368827
14.

Migraine association and linkage studies of an endothelial nitric oxide synthase (NOS3) gene polymorphism.

Griffiths LR, Nyholt DR, Curtain RP, Goadsby PJ, Brimage PJ.

Neurology. 1997 Aug;49(2):614-7. Erratum in: Neurology 1997 Nov;49(5):1489.

PMID:
9270610
15.

Migraine association and linkage analyses of the human 5-hydroxytryptamine (5HT2A) receptor gene.

Nyholt DR, Curtain RP, Gaffney PT, Brimage P, Goadsby PJ, Griffiths LR.

Cephalalgia. 1996 Nov;16(7):463-7.

PMID:
8933989
16.

Cross-sectional study of a microsatellite marker in the low density lipoprotein receptor gene in obese normotensives.

Griffiths LR, Nyholt DR, Curtain RP, Gaffney PT, Morris BJ.

Clin Exp Pharmacol Physiol. 1995 Jun-Jul;22(6-7):496-8.

PMID:
8582115
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