1. The serum porphobilonogen and hepatic porphobilinogen deaminase in normal and porphyric individuals;Miyagi;J Lab Clin Med,1971
2. Heme biosynthesis in intermittent acute porphyria. Decreased hepatic conversion of porphobilinogen to porphyrins and increased delta aminolevulinic acid synthetase activity;Strand,1970
3. Decreased red cell uroporphyrinogen-I synthetase in intermittent acute porphyria;Strand;J Clin Invest,1972
4. Intermittent acute porphyria. Demonstration of a genetic defect in porphobilinogen metabolism;Meyer;N Engl J Med,1972
5. A microassay for uroporphyrinogen-I synthase, one of three abnormal enzyme activities in acute intermittent porphyria, and its application to the study of the genetics of this disease;Sassa,1974