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6. Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissues. Endres W; Schaller R; Shin YS J Inherit Metab Dis; 1984; 7(1):8. PubMed ID: 6429443 [No Abstract] [Full Text] [Related]
7. Argininemia: report of a new case and mechanisms of orotic aciduria and hyperammonemia. Yoshino M; Kubota K; Yoshida I; Murakami T; Yamashita F Adv Exp Med Biol; 1982; 153():121-5. PubMed ID: 7164892 [No Abstract] [Full Text] [Related]
9. Use of enzyme-loaded erythrocytes in in-vitro correction of arginase-deficient erythrocytes in familial hyperargininemia. Adriaenssens K; Karcher D; Lowenthal A; Terheggen HG Clin Chem; 1976 Mar; 22(3):323-6. PubMed ID: 1253407 [TBL] [Abstract][Full Text] [Related]
10. [Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies]. Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP Z Kinderheilkd; 1970; 107(4):298-312. PubMed ID: 5438971 [No Abstract] [Full Text] [Related]
11. Biochemical diagnosis and follow-up in a new Italian patient with hyperargininaemia. Gatti R; Cerone R; Caruso U; Schiaffino MC; Ciccone O J Inherit Metab Dis; 1993; 16(6):1050. PubMed ID: 8127059 [No Abstract] [Full Text] [Related]
12. Hyperargininemia: clinical course and treatment with sodium benzoate and phenylacetic acid. Mizutani N; Maehara M; Hayakawa C; Kato T; Watanabe K; Suzuki S Brain Dev; 1983; 5(6):555-63. PubMed ID: 6670711 [TBL] [Abstract][Full Text] [Related]
13. Hyperargininemia, epilepsy and the metabolism of guanidino compounds. Wiechert P; Marescau B; De Deyn PP; Lowenthal A Padiatr Grenzgeb; 1989; 28(2):101-6. PubMed ID: 2657590 [TBL] [Abstract][Full Text] [Related]
14. Arginase deficiency in multiple tissues in argininemia. Michels VV; Beaudet AL Clin Genet; 1978 Jan; 13(1):61-7. PubMed ID: 624188 [TBL] [Abstract][Full Text] [Related]
15. Argininemia: a treatable genetic cause of progressive spastic diplegia simulating cerebral palsy: case reports and literature review. Prasad AN; Breen JC; Ampola MG; Rosman NP J Child Neurol; 1997 Aug; 12(5):301-9. PubMed ID: 9378897 [TBL] [Abstract][Full Text] [Related]
16. Human hyperargininemia: a mutation not expressed in skin fibroblasts? Van Elsen AF; Leroy JG Am J Hum Genet; 1977 Jul; 29(4):350-5. PubMed ID: 879168 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapy. Marescau B; De Deyn PP; Lowenthal A; Qureshi IA; Antonozzi I; Bachmann C; Cederbaum SD; Cerone R; Chamoles N; Colombo JP Pediatr Res; 1990 Mar; 27(3):297-303. PubMed ID: 1690873 [TBL] [Abstract][Full Text] [Related]
19. Ammonia metabolism in a family affected by hyperargininemia. Qureshi IA; Letarte J; Ouellet R; Lelièvre M; Laberge C Diabete Metab; 1981 Mar; 7(1):5-11. PubMed ID: 7238975 [TBL] [Abstract][Full Text] [Related]