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Neurology|February 17, 2010
CLN5 mutations are frequent in juvenile and late-onset non-Finnish patients with NCLW Xin, T E Mullen, R Kiely, et al.Neurology|February 17, 2010
Accuracy of clinical signs, SEP, and EEG in predicting outcome of hypoxic coma: a meta-analysisY C Lee, T G Phan, D J Jolley, et al.Neurology|February 17, 2010
Risk of recurrent stroke, myocardial infarction, or death in hospitalized stroke patientsWuwei Feng, Robert M Hendry, Robert J AdamsNeurology|December 29, 2005
Prodromal cognitive signs of dementia in 85-year-olds using four sources of informationS Sacuiu, M Sjögren, B Johansson, et al.Neurology|December 29, 2005
The natural history of primary progressive MS in British Columbia, CanadaHelen Tremlett, Donald Paty, Virginia DevonshireNeurology|December 29, 2005
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 geneH Jungbluth, H Zhou, L Hartley, et al.Neurology|December 29, 2005
Elevated IL-6 and TNF-alpha levels in patients with ALS: inflammation or hypoxia?C Moreau, D Devos, V Brunaud-Danel, et al.Neurology|December 31, 2005
Premorbid antiplatelet use and ischemic stroke outcomesN Sanossian, J L Saver, V Rajajee, et al.Neurology|December 31, 2005
Seizure control and treatment in pregnancy: observations from the EURAP epilepsy pregnancy registryNeurology|December 31, 2005
Albendazole trial at 15 or 30 mg/kg/day for subarachnoid and intraventricular cysticercosisF Göngora-Rivera, J L Soto-Hernández, D González Esquivel, et al.Pageof 2,610