M.O. McCarron
Department of Neuropathology
University of Glasgow
Institute of Neurological Sciences
Southern General Hospital
UK
Name/email consistency: medium
- Apolipoprotein E genotype and cerebral amyloid angiopathy-related hemorrhage. McCarron, M.O., Nicoll, J.A. Ann. N. Y. Acad. Sci. (2000)
- Chronic vitamin E deficiency causing spinocerebellar degeneration, peripheral neuropathy, and centro-cecal scotomata. McCarron, M.O., Russell, A.J., Metcalfe, R.A., Deysilva, R. Nutrition (1999)
- Cerebral amyloid angiopathy-related hemorrhage. Interaction of APOE epsilon2 with putative clinical risk factors. McCarron, M.O., Nicoll, J.A., Ironside, J.W., Love, S., Alberts, M.J., Bone, I. Stroke (1999)
- APOE genotype as a risk factor for ischemic cerebrovascular disease: a meta-analysis. McCarron, M.O., Delong, D., Alberts, M.J. Neurology (1999)
- Intracerebral hemorrhage outcome: apolipoprotein E genotype, hematoma, and edema volumes. McCarron, M.O., Hoffmann, K.L., DeLong, D.M., Gray, L., Saunders, A.M., Alberts, M.J. Neurology (1999)
- High frequency of apolipoprotein E epsilon 2 allele is specific for patients with cerebral amyloid angiopathy-related haemorrhage. McCarron, M.O., Nicoll, J.A. Neurosci. Lett. (1998)
