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Neurology|February 1, 1997
Validation of the ACAS TIA/stroke algorithmP N Karanjia, J J Nelson, D S Lefkowitz, et al.Neurology|February 1, 1997
Cerebrospinal fluid creatine kinase BB isoenzyme activity and neurologic prognosis after cardiac arrestD L Tirschwell, W T Longstreth, M E Rauch-Matthews, et al.Neurology|February 1, 1997
Comparison of extrapyramidal features in 31 pathologically confirmed cases of diffuse Lewy body disease and 34 pathologically confirmed cases of Parkinson's diseaseE D Louis, L A Klatka, Y Liu, et al.Neurology|February 1, 1997
Survival of patients with pathologically proven multiple system atrophy: a meta-analysisY Ben-Shlomo, G K Wenning, F Tison, et al.Neurology|February 1, 1997
Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossaB Subramaniam, S Naidu, A L ReissNeurology|February 1, 1997
A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsiesP Young, H Wiebusch, F Stögbauer, et al.Neurology|February 1, 1997
Dose-dependent, central effects of botulinum neurotoxin type A: a pilot study in the alert behaving catB Moreno-López, A M Pastor, R R de la Cruz, et al.Neurology|February 1, 1997
A novel point mutation in the peripheral myelin protein 22 (PMP22) gene associated with Charcot-Marie-Tooth disease type 1AM G Marrosu, S Vaccargiu, G Marrosu, et al.Neurology|February 1, 1997
Torsional eye movements in patients with skew deviation and spasmodic torticollis: responses to static and dynamic head rollL Averbuch-Heller, K G Rottach, A Z Zivotofsky, et al.Neurology|February 1, 1997
Apolipoprotein E-epsilon 2 and Alzheimer's disease: genotype influences pathologic phenotypeC F Lippa, T W Smith, A M Saunders, et al.Pageof 2,608