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Journal Abstract Search

66 related items for PubMed ID: 3419873

  • 1. [Partial ornithine carbamyl transferase deficiency].
    Largillière C.
    Pediatrie; 1988; 43(4):309-12. PubMed ID: 3419873
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
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  • 3. Central pontine myelinolysis as a complication of partial ornithine carbamoyl transferase deficiency.
    Mattson LR, Lindor NM, Goldman DH, Goodwin JT, Groover RV, Vockley J.
    Am J Med Genet; 1995 Jun 19; 60(3):210-3. PubMed ID: 7573173
    [Abstract] [Full Text] [Related]

  • 4. 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 19; 85 Suppl 2():S720-31. PubMed ID: 12403252
    [Abstract] [Full Text] [Related]

  • 5. Ornithine transcarbamylase deficiency. Unsuccessful therapy of neonatal hyperammonemia with N-carbamyl-L-glutamate and L-arginine.
    Gelehrter TD, Rosenberg LE.
    N Engl J Med; 1975 Feb 13; 292(7):351-2. PubMed ID: 1117963
    [No Abstract] [Full Text] [Related]

  • 6. [Changes of urinary excretion of orotic acid in a patient with ornithine carbamyl transferase deficiency].
    Sakane Y, Sugimoto T.
    Rinsho Byori; 1982 May 13; 30(5):547-50. PubMed ID: 7131821
    [No Abstract] [Full Text] [Related]

  • 7. [Hereditary ornithine-carbamyl-transferase deficiency with qualitative enzyme abnormality. Report of a form with neonatal revelation and fatal course in a boy].
    Saudubray JM, Cathelineau L, Charpentier C, Boisse J, Allaneau C, Le Bont H, Lesage B.
    Arch Fr Pediatr; 1973 Jan 13; 30(1):15-27. PubMed ID: 4721585
    [No Abstract] [Full Text] [Related]

  • 8. Therapy of urea cycle enzymopathies: three case studies.
    Batshaw ML, Painter MJ, Sproul GT, Schafer IA, Thomas GH, Brusilow S.
    Johns Hopkins Med J; 1981 Jan 13; 148(1):34-40. PubMed ID: 7453005
    [No Abstract] [Full Text] [Related]

  • 9. [Hyperammonemia in the newborn through ornithine transcarbamylase deficiency (author's transl)].
    Plöchl E, Hilbe W, Bachmann C.
    Padiatr Padol; 1981 Jan 13; 16(2):179-88. PubMed ID: 7243329
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  • 11. Effect of long-term administration of sodium benzoate to a patient with partial ornithine carbamoyl transferase deficiency.
    Takeda E, Kuroda Y, Toshima K, Watanabe T, Naito E, Miyao M.
    Clin Pediatr (Phila); 1983 Mar 13; 22(3):206-8. PubMed ID: 6825366
    [Abstract] [Full Text] [Related]

  • 12. [Living related liver transplantation for patients with ornithine transcarbamylase deficiency].
    Tazuke M, Murakawa M, Nakao S, Mukaida K, Toda H, Mori K.
    Masui; 1997 Jun 13; 46(6):783-7. PubMed ID: 9223881
    [Abstract] [Full Text] [Related]

  • 13. [Carbamyl phosphate synthase deficiency: clinical symptoms, diagnosis and dietary-medicamentous treatment in the neonatal period and infancy].
    Hochreutener H, Issakainen J, Bachmann C, Baerlocher K.
    Helv Paediatr Acta; 1989 Jun 13; 43(5-6):493-505. PubMed ID: 2745145
    [Abstract] [Full Text] [Related]

  • 14. [Congenital hyperammoniemia caused by ornithine carbamoyl-transferase and carbamyl phosphate synthetase deficiency].
    Salle B, Levin B, Longin B, Richard P, Andre M, Gauthier J.
    Arch Fr Pediatr; 1972 May 13; 29(5):493-504. PubMed ID: 4655647
    [No Abstract] [Full Text] [Related]

  • 15. Hyperammoniemic coma in an adolescent girl: an unusual case of ornithine transcarbamylase deficiency.
    Perini M, Zarcone D, Corbetta C.
    Ital J Neurol Sci; 1993 Sep 13; 14(6):461-4. PubMed ID: 8282523
    [Abstract] [Full Text] [Related]

  • 16. [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 13; 16(5):416-20. PubMed ID: 7114619
    [Abstract] [Full Text] [Related]

  • 17. Sodium valproate and ornithine carbamyl transferase deficiency.
    Tripp JH, Hargreaves T, Anthony PP, Searle JF, Miller P, Leonard JV, Patrick AD, Oberholzer VG.
    Lancet; 1981 May 23; 1(8230):1165-6. PubMed ID: 6112522
    [No Abstract] [Full Text] [Related]

  • 18. [Hyperammonemia type II as an example of urea cycle disorder].
    Hawrot-Kawecka AM, Kawecki GP, Duława J.
    Wiad Lek; 2006 May 23; 59(7-8):512-5. PubMed ID: 17209350
    [Abstract] [Full Text] [Related]

  • 19. Focal glycogenosis of the liver in disorders of ureagenesis: its occurrence and diagnostic significance.
    Badizadegan K, Perez-Atayde AR.
    Hepatology; 1997 Aug 23; 26(2):365-73. PubMed ID: 9252147
    [Abstract] [Full Text] [Related]

  • 20. [Congenital deficiency of ornithine transcarbamylase. Description of 2 clinical cases].
    D'Eufemia P, Corrado G, Sabetta G, Castro M, Martino F, Cantani A, Ruberto U.
    Minerva Pediatr; 1983 Mar 15; 35(5):219-24. PubMed ID: 6343831
    [No Abstract] [Full Text] [Related]

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