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Journal Abstract Search

378 related items for PubMed ID: 729890

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  • 3. [Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)].
    Beaudry MA, Letarte J, Collu R, Leboeuf G, Ducharme JR, Melancon SB, Dallairf L.
    Diabete Metab; 1975 Mar; 1():29-37. PubMed ID: 1234064
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  • 5. Transient hyperammonemia during aging in ornithine transcarbamylase-deficient, sparse-fur mice.
    Gushiken T, Yoshimura N, Saheki T.
    Biochem Int; 1985 Nov; 11(5):637-43. PubMed ID: 4091843
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  • 6. [Variability of enzyme activity and urinary orotic acid in ornithine transcarbamylase deficient spf/+ heterozygotic mice].
    Qureshi IA, Letarte J, Lebel S, Ouellet R.
    Diabete Metab; 1986 Oct; 12(5):250-5. PubMed ID: 3803679
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  • 8. Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.
    Sunshine P, Lindenbaum JE, Levy HL, Freeman JM.
    Pediatrics; 1972 Jul; 50(1):100-11. PubMed ID: 5038084
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  • 9. Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndrome.
    Brown T, Hug G, Lansky L, Bove K, Scheve A, Ryan M, Brown H, Schubert WK, Partin JC, Lloyd-Still J.
    N Engl J Med; 1976 Apr 15; 294(16):861-7. PubMed ID: 175276
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  • 10. Heterogeneity of patients with late onset ornithine transcarbamylase deficiency.
    Tuchman M, Holzknecht RA.
    Clin Invest Med; 1991 Aug 15; 14(4):320-4. PubMed ID: 1782729
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  • 11. [A new family with mutation of the structural gene of human ornithine carbamoyltransferase].
    Stoll C, Bieth R, Dreyfus J, Flori E, Lutz P, Levy JM.
    Arch Fr Pediatr; 1978 May 15; 35(5):512-8. PubMed ID: 678030
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  • 12. Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase.
    Matsuda I, Arashima S, Nambu H, Takekoshi Y, Anakura M.
    Pediatrics; 1971 Oct 15; 48(4):595-600. PubMed ID: 5114747
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  • 13. Urea-cycle enzyme deficiencies and an increased nitrogen load producing hyperammonemia in Reye's syndrome.
    Snodgrass PJ, DeLong GR.
    N Engl J Med; 1976 Apr 15; 294(16):855-60. PubMed ID: 1250313
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  • 14. Congenital hyperammonemia: symptomatic carrier girl patient and her asymptomatic heterozygous mother for ornithine transcarbamylase (OTC) deficiency: specific enzyme diagnostic and kinetic investigations for the detection of heterozygous genostatus.
    László A, Karsai T, Várkonyi A.
    Acta Paediatr Hung; 1991 Apr 15; 31(3):291-7. PubMed ID: 1742044
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  • 15. [Neonatal hyperammonemia due to ornithine transcarbamylase deficiency (author's transl)].
    del Valle JA, Urbón A, García MJ, Cuadrado P, Ugarte M.
    An Esp Pediatr; 1982 May 15; 16(5):416-20. PubMed ID: 7114619
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