L R Griffiths
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Explore the profile of L R Griffiths including associated specialties, affiliations and a list of published articles.
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Recent Articles
11.
Yogeetha B, Haupt L, McKenzie K, Sutherland H, Okolicsyani R, Lea R, et al.
Mol Biol Rep
. 2013 Aug;
40(9):5483-90.
PMID: 23918043
Here, we investigate the genetic basis of human memory in healthy individuals and the potential role of two polymorphisms, previously implicated in memory function. We have explored aspects of retrospective...
12.
Maher B, Taylor M, Stuart S, Okolicsanyi R, Roy B, Sutherland H, et al.
Gene
. 2013 Aug;
528(2):343-6.
PMID: 23911303
Migraine is a common neurological disorder characterised by temporary disabling attacks of severe head pain and associated disturbances. There is significant evidence to suggest a genetic aetiology to the disease...
13.
Gasparini C, Griffiths L
Int J Biomed Sci
. 2013 May;
9(1):1-8.
PMID: 23675283
Migraine is a common genetically linked neurovascular disorder. Approximately ∼12% of the Caucasian population are affected including 18% of adult women and 6% of adult men (1, 2). A notable...
14.
Sutherland H, Buteri J, Menon S, Haupt L, MacGregor E, Lea R, et al.
Gene
. 2012 Dec;
515(1):187-92.
PMID: 23237777
Migraine is a common neurovascular brain disorder characterised by recurrent attacks of severe headache that may be accompanied by various neurological symptoms. Migraine is thought to result from activation of...
15.
Stuart S, Griffiths L
Mol Genet Genomics
. 2012 Oct;
287(11-12):837-44.
PMID: 23052833
Migraine is a common neurological disorder characterised by debilitating head pain and an assortment of additional symptoms which can include nausea, emesis, photophobia, phonophobia and occasionally visual sensory disturbances. Migraine...
16.
Donges B, Haupt L, Lea R, Chan R, Shum D, Griffiths L
Gene
. 2012 Jul;
506(1):135-40.
PMID: 22771913
Human memory is a complex neurocognitive process. By combining psychological and molecular genetics expertise, we examined the APOE ε4 allele, a known risk factor for Alzheimer's disease, and the COMT...
17.
Menon S, Lea R, Roy B, Hanna M, Wee S, Haupt L, et al.
J Headache Pain
. 2012 Jul;
13(7):513-9.
PMID: 22752568
Migraine is a painful and debilitating, neurovascular disease. Current migraine head pain treatments work with differing efficacies in migraineurs. The opioid system plays an important role in diverse biological functions...
18.
Roy B, Maksemous N, Smith R, Menon S, Davies G, Griffiths L
Mutat Res
. 2012 Mar;
732(1-2):3-8.
PMID: 22373597
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary disease of small vessel caused by mutations in the NOTCH3 gene (NCBI Gene ID: 4854) located on...
19.
Maher B, Kerr M, Cox H, MacMillan J, Brimage P, Esposito T, et al.
Neurogenetics
. 2012 Feb;
13(1):97-101.
PMID: 22294494
Investigations into migraine genetics have suggested that susceptibility loci exist on the X chromosome. These reports are supported by evidence that demonstrates male probands as having a higher proportion of...
20.
Tiralongo E, Lea R, Wee S, Hanna M, Griffiths L
Evid Based Complement Alternat Med
. 2012 Jan;
2012:417267.
PMID: 22229040
Objective. To identify whether a standardised Echinacea formulation is effective in the prevention of respiratory and other symptoms associated with long-haul flights. Methods. 175 adults participated in a randomised, double-blind...