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4. 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]
5. Molecular basis of phenotypic variation in patients with argininemia. Uchino T; Snyderman SE; Lambert M; Qureshi IA; Shapira SK; Sansaricq C; Smit LM; Jakobs C; Matsuda I Hum Genet; 1995 Sep; 96(3):255-60. PubMed ID: 7649538 [TBL] [Abstract][Full Text] [Related]
6. [Seven patients of argininemia with spastic tetraplegia as the first and major symptom and prenatal diagnosis of two fetuses with high risk]. Wu T; Li X; Ding Y; Liu Y; Song J; Wang Q; Li M; Qin Y; Yang Y Zhonghua Er Ke Za Zhi; 2015 Jun; 53(6):425-30. PubMed ID: 26310552 [TBL] [Abstract][Full Text] [Related]
7. Arginase and free amino acids in hyperargininemia: leukocyte arginine as a diagnostic parameter for heterozygotes. Marescau B; Pintens J; Lowenthal A; Terheggen HG; Adriaenssens K J Clin Chem Clin Biochem; 1979 Apr; 17(4):211-7. PubMed ID: 438730 [TBL] [Abstract][Full Text] [Related]
8. Clinical and biochemical studies on periodic hyperammonemia with hyperlysinemia and homocitrullinuria. Oyanagi K; Sogawa H; Sato S; Orii T; Nakao T Tohoku J Exp Med; 1976 Oct; 120(2):105-12. PubMed ID: 982431 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Late diagnosis of congenital argininemia during administration of sodium valproate]. Christmann D; Hirsch E; Mutschler V; Collard M; Marescaux C; Colombo JP Rev Neurol (Paris); 1990; 146(12):764-6. PubMed ID: 2291040 [TBL] [Abstract][Full Text] [Related]
12. Hyperargininaemia: follow-up of a new case. Scarpa P; Faggioli R J Inherit Metab Dis; 1995; 18(1):80-1. PubMed ID: 7623450 [No Abstract] [Full Text] [Related]
13. Argininosuccinic aciduria: metabolic studies and effects of treatment with keto-analogues of essential amino acids. Böhles H; Heid H; Harms D; Schmid D; Fekl W Eur J Pediatr; 1978 Jul; 128(4):225-33. PubMed ID: 668730 [TBL] [Abstract][Full Text] [Related]
14. Five novel mutations in ARG1 gene in Chinese patients of argininemia. Wu TF; Liu YP; Li XY; Wang Q; Ding Y; Ma YY; Song JQ; Yang YL Pediatr Neurol; 2013 Aug; 49(2):119-23. PubMed ID: 23859858 [TBL] [Abstract][Full Text] [Related]
15. Enzyme replacement therapy in a patient with hyperargininemia. Mizutani N; Hayakawa C; Maehara M; Watanabe K Tohoku J Exp Med; 1987 Mar; 151(3):301-7. PubMed ID: 3590176 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Arginase deficiency in Macaca fascicularis. I. Arginase activity and arginine concentration in erythrocytes and liver. Shih VE; Jones TC; Levy HL; Madigan PM Pediatr Res; 1972 Jun; 6(6):548-51. PubMed ID: 4625814 [No Abstract] [Full Text] [Related]
18. 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]
19. Prenatal diagnosis for arginase deficiency: a case study. Hewson S; Clarke JT; Cederbaum S J Inherit Metab Dis; 2003; 26(6):607-10. PubMed ID: 14605507 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]