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4. [Prenatal diagnosis of enzymopathies of the urea cycle]. Chadefaux B; Rabier D; Kamoun P Ann Biol Clin (Paris); 1988; 46(7):471-6. PubMed ID: 3056128 [TBL] [Abstract][Full Text] [Related]
5. Plasma alpha-ketoglutarate in urea cycle enzymopathies and its role as a harbinger of hyperammonemic coma. Batshaw ML; Walser M; Brusilow SW Pediatr Res; 1980 Dec; 14(12):1316-9. PubMed ID: 7208146 [TBL] [Abstract][Full Text] [Related]
14. The activity of carbamoyl-phosphate synthetase I and ornithine carbamoyltransferase (OCT) in the intestine and screening for OCT deficiency in the rectal mucosa. Matsushima A; Orii T J Inherit Metab Dis; 1981; 4(2):83-4. PubMed ID: 6790859 [No Abstract] [Full Text] [Related]
15. Management of heritable disorders of the urea cycle and of Refsum's and Fabry's diseases. Moser HW; Batshaw ML; Murray C; Braine H; Brusilow SW Prog Clin Biol Res; 1979; 34():183-200. PubMed ID: 93755 [No Abstract] [Full Text] [Related]