New observations provide a neural link between the perception of visual objects and the subsequent storage of visual information in working memory. Supèrprovides unique insights into this crucial area of memory function and the neurologic symptoms that occur when these functions are altered.
Activation of spinal cord circulation independent of the higher centers is an emerging and dynamic area of neuroscience and clinical neurology. Kalbprovides the neurobiologic basis for autonomous spinal cord functioning and potential therapies.
Levels of 14-3-3 protein in cerebrospinal fluid may be helpful to diagnose Creutzfeldt-Jakob disease, but we must be aware of false-negatives and false-positives and the wider spectrum of differential diagnoses, as emphasized by Geschwind and colleagues. Editorial perspective is provided by Allen J. Aksamit, MD.
As emphasized by Burneo and colleagues, patients with extratemporal porencephaly and intractable seizures should be evaluated early and considered for temporal lobectomy if findings on clinical examination, magnetic resonance imaging, and electroencephalogram support seizures of temporal lobe onset.
Farlow and colleaguesshow that after discontinuation of therapy, patients treated with rivastigmine exhibited less deterioration in cognitive functions compared with patients receiving a placebo. The use of this drug is defined and refined in this interesting clinical trial.
This prospective study by Teunissen and colleaguesshows a slow deterioration of muscle strength and an increase in disability in patients with type 2 Charcot-Marie-Tooth disease during a 5-year follow-up period.
Quality of life scores in 27 patients. Deviations from the reference population (zero line) are expressed in mean standard scores. Greater deviation of the zero line indicates greater limitations. The x-axis values represent the domains of the RAND 36-item health survey questionnaire.
Inheritance of the apolipoprotein E ϵ4 allele is associated with an increased risk for late posttraumatic seizures as detailed by Diaz-Arrastia and colleagues.
Lee and colleaguesprovide the first detailed analysis of the clinical characteristics of the genetically defined CAG repeat spinocerebellar ataxias in Korean patients. An important clinical and molecular correlation defines the natural history of disease in these patients.
This Month in Archives of Neurology. Arch Neurol. 2003;60(6):802. doi:10.1001/archneur.60.6.802