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In a large study comparing different strategies for screening for Down's syndrome, first-trimester combined screening (measurement of nuchal translucency, pregnancy-associated plasma protein A [PAPP-A], and the free beta subunit of human chorionic gonadotropin [fβhCG]) at 11 weeks was better than second-trimester quadruple screening (measurement of alpha-fetoprotein, hCG, unconjugated estriol, and inhibin A). Strategies combining first-trimester and second-trimester screening provide high detection rates at acceptable false positive rates. These findings will help guide the choice of screening strategies for Down's syndrome.
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A small proportion of glioblastomas respond to gefitinib or erlotinib (tyrosine kinase inhibitors). Some of these responsive tumors have a mutant variant of the epidermal growth factor receptor (EGFR), and some unresponsive tumors lack PTEN, a regulator of the pathway that a mutant EGFR activates. The simultaneous presence in glioblastoma cells of mutant EGFR and PTEN was associated with responsiveness to tyrosine kinase inhibitors.
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Central sleep apnea is common among patients who have heart failure and increases the risk of death in this setting. In the Canadian Continuous Positive Airway Pressure trial, continuous positive airway pressure (CPAP) therapy administered to patients with heart failure was found to reduce the severity of central sleep apnea and increase the left ventricular ejection fraction, but did not improve survival.
Obstructive sleep apnea is a form of sleep-disordered breathing in which the upper airway closes repeatedly during sleep. In an observational cohort study, the risk of stroke or death from any cause was significantly increased among patients with sleep apnea, independent of other cardiovascular risk factors. More severe sleep apnea was associated with greater risk.
A rash developed in a 10-year-old girl and became confluent and bullous, with sloughing, after she was given carbamazepine for a seizure. Oral and conjunctival sloughing followed, with pancytopenia, gastrointestinal hemorrhage, and respiratory failure. After a protracted course of management in the burn unit, reepithelialization occurred, and the patient recovered fully.
Although we have successfully sequenced the human genome, progress toward defining the genetic basis of disease has been limited by the availability of people willing to share their phenotypic information along with their genotypic information. In this article, the authors offer a proposal to increase participation in genetic studies.
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