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Journal Abstract Search

166 related items for PubMed ID: 2929667

  • 21.
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  • 22. Hyperornithinemia, hyperammonemia, and homocitrullinuria associated with decreased carbamyl phosphate synthetase I activity.
    Gatfield PD, Taller E, Wolfe DM, Haust MD.
    Pediatr Res; 1975 May; 9(5):488-97. PubMed ID: 166348
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  • 23. Abnormal urinary excretion of polyamines in HHH syndrome (hyperornithinemia associated with hyperammonemia and homocitrullinuria).
    Shimizu H, Maekawa K, Eto Y.
    Brain Dev; 1990 May; 12(5):533-5. PubMed ID: 2288388
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  • 24. 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 15; 218(1-2):53-8. PubMed ID: 14759633
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  • 25. 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 15; 10(2):78-82. PubMed ID: 862180
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  • 26.
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  • 27. Hyperornithinemia, hyperammonemia and homocitrullinuria--a case report and study of ornithine metabolism using in vivo deuterium labelling.
    Tsujino S, Suzuki T, Azuma T, Higa S, Sakoda S, Kishimoto S.
    Clin Chim Acta; 1991 Sep 14; 201(1-2):129-33. PubMed ID: 1790616
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  • 30. Possible pathogenetic mechanism in hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome.
    Haust MD, Gordon BA.
    Birth Defects Orig Artic Ser; 1987 Sep 14; 23(1):17-45. PubMed ID: 3580547
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  • 31. Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15.
    Debray FG, Lambert M, Lemieux B, Soucy JF, Drouin R, Fenyves D, Dubé J, Maranda B, Laframboise R, Mitchell GA.
    J Med Genet; 2008 Nov 14; 45(11):759-64. PubMed ID: 18978333
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  • 32.
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  • 33. Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with stroke-like imaging presentation: clinical, biochemical and molecular analysis.
    Al-Hassnan ZN, Rashed MS, Al-Dirbashi OY, Patay Z, Rahbeeni Z, Abu-Amero KK.
    J Neurol Sci; 2008 Jan 15; 264(1-2):187-94. PubMed ID: 17825324
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  • 34. A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet.
    Gjessing LR, Lunde HA, Undrum T, Broch H, Alme A, Lie SO.
    J Inherit Metab Dis; 1986 Jan 15; 9(2):186-92. PubMed ID: 3091924
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  • 35. Defective ornithine metabolism in the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria.
    Shih VE, Mandell R, Herzfeld A.
    J Inherit Metab Dis; 1981 Jan 15; 4(2):95-6. PubMed ID: 6790865
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  • 39. Conscientious metabolic monitoring on a patient with hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome undergoing anaesthesia.
    Mühling J, Dehne MG, Fuchs M, Sablotzki A, Weiss S, Spatz J, Hempelmann G.
    Amino Acids; 2001 Jan 15; 21(3):303-18. PubMed ID: 11764411
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