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Neurology|June 13, 2001
Bcl-2 family protein behavior in frontotemporal dementia implies vascular involvementK E Nichol, R Kim, C W CotmanNeurology|April 26, 2001
Neuropsychological assessment in children with absence epilepsyP Pavone, R Bianchini, R R Trifiletti, et al.Neurology|April 26, 2001
Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain diseaseB Cormand, H Pihko, M Bayés, et al.Neurology|April 26, 2001
Increased CSF cortisol in AD is a function of APOE genotypeE R Peskind, C W Wilkinson, E C Petrie, et al.Neurology|April 26, 2001
No correlation between muscle A3243G mutation load and mitochondrial function in vivoP F Chinnery, D J Taylor, D Manners, et al.Neurology|October 10, 2001
In vivo hippocampal glucose metabolism in mesial temporal lobe epilepsyR C Knowlton, K D Laxer, G Klein, et al.Neurology|October 10, 2001
The Clomethiazole Acute Stroke Study in tissue-type plasminogen activator-treated stroke (CLASS-T): final resultsP Lyden, M Jacoby, J Schim, et al.Neurology|October 10, 2001
Small cerebral aneurysms presenting with symptoms other than ruptureJ A Friedman, D G Piepgras, M A Pichelmann, et al.Neurology|October 10, 2001
Sensory symptoms in ipsilateral limbs/body due to lateral medullary infarctionJ S KimNeurology|October 10, 2001
Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL familyP de la Peña, B Bornstein, P del Hoyo, et al.Pageof 2,611