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12. Early dietary management in an infant with argininosuccinase deficiency: preliminary report. Shih VE. J Pediatr; 1972 Apr; 80(4):645-8. PubMed ID: 5015075 [No Abstract] [Full Text] [Related]
13. Establishment of a clonal strain of hepatoma cells which maintain in culture the five enzymes of the urea cycle. Richardson UI, Snodgrass PJ, Nuzum CT, Tashjian AH. J Cell Physiol; 1974 Feb; 83(1):141-9. PubMed ID: 4149774 [No Abstract] [Full Text] [Related]
15. Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase. Matsuda I, Arashima S, Nambu H, Takekoshi Y, Anakura M. Pediatrics; 1971 Oct; 48(4):595-600. PubMed ID: 5114747 [No Abstract] [Full Text] [Related]
16. A neonatal screening test for argininosuccinic acid lyase deficiency and other urea cycle disorders. Talbot HW, Sumlin AB, Naylor EW, Guthrie R. Pediatrics; 1982 Oct; 70(4):526-31. PubMed ID: 7122151 [Abstract] [Full Text] [Related]
17. Hyperammonaemia in 20 families. Biochemical and genetical survey, including investigations in 3 new families. Palmer T, Oberholzer VG, Burgess EA, Butler LJ, Levin B. Arch Dis Child; 1974 Jun; 49(6):443-9. PubMed ID: 4852321 [No Abstract] [Full Text] [Related]