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23. Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: low creatine excretion and effect of citrulline, arginine, or ornithine supplement. Dionisi Vici C; Bachmann C; Gambarara M; Colombo JP; Sabetta G Pediatr Res; 1987 Sep; 22(3):364-7. PubMed ID: 3116497 [TBL] [Abstract][Full Text] [Related]
24. Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH)-syndrome. Ultrastructural changes of mitochondria in cultured dermal fibroblasts of three patients. Haust MD; Dewar RA; Gatfield DP; Gordon BA Pathol Res Pract; 1996 Mar; 192(3):271-80. PubMed ID: 8739474 [TBL] [Abstract][Full Text] [Related]
25. [A case of hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome with spastic paraparesis and severe distal muscle atrophy of lower limbs]. Shigeto H; Yamada T; Kobayashi T; Goto I Rinsho Shinkeigaku; 1992 Jul; 32(7):729-32. PubMed ID: 1291165 [TBL] [Abstract][Full Text] [Related]
27. Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome with evidence of mitochondrial dysfunction due to a novel SLC25A15 (ORNT1) gene mutation in a Palestinian family. Korman SH; Kanazawa N; Abu-Libdeh B; Gutman A; Tsujino S J Neurol Sci; 2004 Mar; 218(1-2):53-8. PubMed ID: 14759633 [TBL] [Abstract][Full Text] [Related]
28. Ornithine methyl ester. An unusual metabolite encountered in the urine of patients with a urea cycle disorder characterized by hyperammonemia, hyperornithinemia and homocitrullinuria. Gordon BA; Gatfield PD; Taller E Clin Biochem; 1977 Apr; 10(2):78-82. PubMed ID: 862180 [TBL] [Abstract][Full Text] [Related]
29. Reduced ornithine catabolism in cultured fibroblasts and phytohaemagglutinin-stimulated lymphocytes from a patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria. Gray RG; Hill SE; Pollitt RJ Clin Chim Acta; 1982 Feb; 118(2-3):141-8. PubMed ID: 6120052 [No Abstract] [Full Text] [Related]
33. Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuria. Haust MD; Gatfield PD; Gordon BA Hum Pathol; 1981 Mar; 12(3):212-22. PubMed ID: 7228016 [TBL] [Abstract][Full Text] [Related]
34. Homocitrullinuria and homoargininuria in lysinuric protein intolerance. Kato T; Sano M; Mizutani N J Inherit Metab Dis; 1989; 12(2):157-61. PubMed ID: 2474087 [TBL] [Abstract][Full Text] [Related]
35. Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transport. Fell V; Pollitt RJ; Sampson GA; Wright T Am J Dis Child; 1974 May; 127(5):752-6. PubMed ID: 4825593 [No Abstract] [Full Text] [Related]
36. "Basolateral" and mitochondrial membrane transport defect in the hepatocytes in lysinuric protein intolerance. Rajantie J; Simell O; Perheentupa J Acta Paediatr Scand; 1983 Jan; 72(1):65-70. PubMed ID: 6407277 [TBL] [Abstract][Full Text] [Related]
37. Aberrations of ammonia metabolism in ornithine carbamoyltransferase-deficient spf-ash mice and their prevention by treatment with urea cycle intermediate amino acids and an ornithine aminotransferase inactivator. Li MX; Nakajima T; Fukushige T; Kobayashi K; Seiler N; Saheki T Biochim Biophys Acta; 1999 Sep; 1455(1):1-11. PubMed ID: 10524224 [TBL] [Abstract][Full Text] [Related]
38. A neonate with ornithine aminotransferase deficiency; insights on the hyperammonemia-associated biochemical phenotype of gyrate atrophy. Kaczmarczyk A; Baker M; Diddle J; Yuzyuk T; Valle D; Lindstrom K Mol Genet Metab Rep; 2022 Jun; 31():100857. PubMed ID: 35782604 [TBL] [Abstract][Full Text] [Related]
39. Hyperammonemia caused by impaired mitochondrial ornithine transport in a patient with partial quantitative deficiency of ornithine carbamoyltransferase. Kuno T; Miyazaki S; Inoue I; Saheki T Clin Biochem; 1990 Apr; 23(2):143-7. PubMed ID: 2372929 [TBL] [Abstract][Full Text] [Related]
40. Possible pathogenetic mechanism in hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome. Haust MD; Gordon BA Birth Defects Orig Artic Ser; 1987; 23(1):17-45. PubMed ID: 3580547 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]