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1 Reye's syndrome (RS) appeared suddenly in the 1950s and
2 Reye's syndrome is characterized by encephalopathy and f
3 tabolic disorders of ureagenesis can cause a Reye-like syndrome with potentially fatal hyperammonemia
5 ar-old, previously healthy boy who died of a Reye-like episode and cerebellar stroke triggered by a m
6 ially narrow the differential diagnosis of a Reye-like syndrome with diffuse hepatocellular steatosis
7 nts and children-such as biliary atresia and Reye's syndrome; and (3) redefinition of the once obscur
15 ar aggregates of this nature do not occur in Reye syndrome or in any of its metabolic mimics other th
16 ked to several metabolic diseases, including Reye's syndrome, which is aspirin-induced hepatotoxicity
20 ance years 1981 through 1997), 1207 cases of Reye's syndrome were reported in patients less than 18 y