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Journal Abstract Search

105 related items for PubMed ID: 1883110

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  • 4. The diagnosis of ornithine transcarbamylase deficiency.
    Batshaw ML.
    J Pediatr Gastroenterol Nutr; 1985 Feb; 4(1):4-6. PubMed ID: 3981367
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  • 6. Cerebral dysfunction in asymptomatic carriers of ornithine transcarbamylase deficiency.
    Batshaw ML, Roan Y, Jung AL, Rosenberg LA, Brusilow SW.
    N Engl J Med; 1980 Feb 28; 302(9):482-5. PubMed ID: 7351973
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  • 8. Ornithine transcarbamylase deficiency: case report and review.
    Bueno JD, Lutz R, Cho S.
    Kans Med; 1995 Feb 28; 96(3):135-8. PubMed ID: 8583741
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  • 10. Ornithine transcarbamylase deficiency: ten new mutations and high proportion of de novo mutations in heterozygous females.
    Oppliger Leibundgut E, Liechti-Gallati S, Colombo JP, Wermuth B.
    Hum Mutat; 1997 Feb 28; 9(5):409-11. PubMed ID: 9143919
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  • 15. Urea cycle disorders in Thai infants: a report of 5 cases.
    Wasant P, Srisomsap C, Liammongkolkul S, Svasti J.
    J Med Assoc Thai; 2002 Aug 28; 85 Suppl 2():S720-31. PubMed ID: 12403252
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  • 17. Natural history of symptomatic partial ornithine transcarbamylase deficiency.
    Rowe PC, Newman SL, Brusilow SW.
    N Engl J Med; 1986 Feb 27; 314(9):541-7. PubMed ID: 3945292
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  • 18. Fatal initial adult-onset presentation of urea cycle defect.
    Lien J, Nyhan WL, Barshop BA.
    Arch Neurol; 2007 Dec 27; 64(12):1777-9. PubMed ID: 18071043
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  • 19. Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family study.
    Treacy EP, Lambert DM, Barnes R, Boriack RL, Vockley J, O'brien LK, Jones PM, Bennett MJ.
    J Pediatr; 2000 Aug 27; 137(2):257-9. PubMed ID: 10931422
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