These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

138 related items for PubMed ID: 219172

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Neonatal hyperammonaemia with complete absence of liver carbamyl phosphate synthetase activity.
    Mantagos S, Tsagaraki S, Burgess EA, Oberholzer V, Palmer T, Sacks J, Baibas S, Valaes T.
    Arch Dis Child; 1978 Mar 15; 53(3):230-4. PubMed ID: 206210
    [Abstract] [Full Text] [Related]

  • 4. Amino acid acylation: a mechanism of nitrogen excretion in inborn errors of urea synthesis.
    Brusilow S, Tinker J, Batshaw ML.
    Science; 1980 Feb 08; 207(4431):659-61. PubMed ID: 6243418
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Severe neonatal deficiency of carbamylphosphate synthetase.
    Lambotte C, Adam A, Van Der Hofstadt J, Dodinval-Versie J, Gielen J.
    Acta Paediatr Belg; 1977 Feb 08; 30(3):151-5. PubMed ID: 204150
    [No Abstract] [Full Text] [Related]

  • 7. Detection of urea cycle enzymopathies in childhood.
    Trauner DA, Self TW.
    Arch Neurol; 1984 Jul 08; 41(7):758-60. PubMed ID: 6743067
    [Abstract] [Full Text] [Related]

  • 8. Focal glycogenosis of the liver in disorders of ureagenesis: its occurrence and diagnostic significance.
    Badizadegan K, Perez-Atayde AR.
    Hepatology; 1997 Aug 08; 26(2):365-73. PubMed ID: 9252147
    [Abstract] [Full Text] [Related]

  • 9. Proceedings: Hepatic ultrastructure in a child with carbamyl phosphate synthetase deficiency, hyperornithinaemia, hyperammonaemia, and homocitrullinuria.
    Haust MD, Gatfield PD.
    Arch Dis Child; 1975 Aug 08; 50(8):663. PubMed ID: 173245
    [No Abstract] [Full Text] [Related]

  • 10. Editorial: Ammonia disposal in Reye's syndrome.
    Smith AL.
    N Engl J Med; 1976 Apr 15; 294(16):897-8. PubMed ID: 1250317
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Double deficiencies of urea cycle enzymes in human liver.
    Raijman L.
    Biochem Med; 1979 Apr 15; 21(2):226-33. PubMed ID: 465019
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [Hyperammonemias of childhood. I. Enzymopathies of the urea cycle].
    Kopieczna-Grzebieniak E, Toborek M, Tarnawski R, Jakubowska D.
    Pediatr Pol; 1987 Oct 15; 62(10):727-32. PubMed ID: 3328149
    [No Abstract] [Full Text] [Related]

  • 16. Disorders of the urea cycle.
    Brusilow SW.
    Hosp Pract (Off Ed); 1985 Oct 15; 20(10):65-72. PubMed ID: 3930543
    [No Abstract] [Full Text] [Related]

  • 17. Prospective treatment of urea cycle disorders.
    Maestri NE, Hauser ER, Bartholomew D, Brusilow SW.
    J Pediatr; 1991 Dec 15; 119(6):923-8. PubMed ID: 1720458
    [Abstract] [Full Text] [Related]

  • 18. [Urea cycle disorders].
    Tazawa Y.
    Ryoikibetsu Shokogun Shirizu; 1995 Dec 15; (8):367-9. PubMed ID: 8581654
    [No Abstract] [Full Text] [Related]

  • 19. Urea cycle enzymopathies.
    Walser M.
    Semin Liver Dis; 1982 Nov 15; 2(4):329-39. PubMed ID: 6763345
    [No Abstract] [Full Text] [Related]

  • 20. [Reye's syndrome].
    Tomaszewski L.
    Pediatr Pol; 1982 Nov 15; 57(11):981-8. PubMed ID: 6763187
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.