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The Review of Scientific Instruments|April 3, 2015
Plasma current start-up by the outer ohmic heating coils in the Saskatchewan TORus Modified (STOR-M) iron core tokamakO Mitarai, C Xiao, D McColl, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 10, 2006
Longitudinal study of the motor response to levodopa in Parkinson's diseaseBenjamin G Clissold, Craig D McColl, Katrina R Reardon, et al.Cellular and Molecular Life Sciences : CMLS|August 29, 2003
Neuronal nicotinic receptors: insights gained from gene knockout and knockin mutant miceJ Drago, C D McColl, M K Horne, et al.British Journal of Haematology|February 26, 2000
Prevalence of the post-thrombotic syndrome in young women with previous venous thromboembolismM D McColl, J Ellison, I A Greer, et al.Neuropharmacology|October 26, 2005
Galanin receptor-1 knockout mice exhibit spontaneous epilepsy, abnormal EEGs and altered inhibition in the hippocampusCraig D McColl, Arie S Jacoby, John Shine, et al.QJM : Monthly Journal of the Association of Physicians|August 31, 2001
Increased oxidative stress in Alzheimer's disease as assessed with 4-hydroxynonenal but not malondialdehydeL T McGrath, B M McGleenon, S Brennan, et al.BJOG : an International Journal of Obstetrics and Gynaecology|April 12, 2000
Prothrombin 20210 G-->A, MTHFR C677T mutations in women with venous thromboembolism associated with pregnancyM D McColl, J Ellison, F Reid, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2009
Longitudinal study of the levodopa motor response in Parkinson's disease: relationship between cognitive decline and motor functionJane E Alty, Benjamin G Clissold, Craig D McColl, et al.Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|May 4, 2011
Pregnancy-specific reference ranges for haematological variables in a Scottish populationR C Shields, V Caric, M Hair, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1997
Asymptomatic coinheritance of heterozygous plasminogen deficiency and the factor VLeiden mutationM D McColl, R C Tait, I D Walker, et al.Pageof 5