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22. A new case of arginase deficiency in a Spanish male. Jordá A; Rubio V; Portolés M; Vilas J; García-Piño J J Inherit Metab Dis; 1986; 9(4):393-7. PubMed ID: 3104676 [TBL] [Abstract][Full Text] [Related]
23. [Hereditary enzyme defects of the urea cycle]. Colombo JP Ergeb Inn Med Kinderheilkd; 1971; 31():97-130. PubMed ID: 4933544 [No Abstract] [Full Text] [Related]
24. Absence of erythrocyte arginase protein in Japanese patients with hyperargininemia. Hayakawa C; Aono S; Keino H; Mizutani N; Watanabe K; Ikemoto M; Totani M; Murachi T; Kashiwamata S Eur J Pediatr; 1991 Sep; 150(11):800-3. PubMed ID: 1959545 [TBL] [Abstract][Full Text] [Related]
25. [Hyperargininemia. Clinical aspects and molecular basis of the defect]. Konarska L Pediatr Pol; 1987 Apr; 62(4):261-72. PubMed ID: 3670917 [No Abstract] [Full Text] [Related]
26. Arginase deficiency in two brothers. Candito M; Bebin B; Vianey-Saban C; Rabier D; Bekri S; Sebag F; Chambon P; Kamoun P J Inherit Metab Dis; 1993; 16(6):1054-6. PubMed ID: 8127062 [No Abstract] [Full Text] [Related]
27. Arginosuccine aciduria. Levin B Am J Dis Child; 1967 Jan; 113(1):162-5. PubMed ID: 6015896 [No Abstract] [Full Text] [Related]
28. Clinical and biochemical findings in argininemia. Terheggen HG; Lowenthal A; Colombo JP Adv Exp Med Biol; 1982; 153():111-9. PubMed ID: 7164891 [No Abstract] [Full Text] [Related]