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

Journal Abstract Search


238 related items for PubMed ID: 4933544

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

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Argininosuccinic aciduria. Neonatal variant with rapid fatal course.
    Carton D, De Schrijver F, Kint J, Van Durme J, Hooft C.
    Acta Paediatr Scand; 1969 Sep; 58(5):528-34. PubMed ID: 5365174
    [No Abstract] [Full Text] [Related]

  • 5. Inherited hyperammonemic syndromes.
    Hsia YE.
    Gastroenterology; 1974 Aug; 67(2):347-74. PubMed ID: 4368001
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [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; 148(1):34-40. PubMed ID: 7453005
    [No Abstract] [Full Text] [Related]

  • 9. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase].
    Cathelineau L, Navarro J, Aymard P, Baudon JJ, Mondet Y, Polonovski C, Laplane R.
    Arch Fr Pediatr; 1972 Jan; 29(7):713-36. PubMed ID: 4644461
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 12. Early dietary management in an infant with argininosuccinase deficiency: preliminary report.
    Shih VE.
    J Pediatr; 1972 Apr; 80(4):645-8. PubMed ID: 5015075
    [No Abstract] [Full Text] [Related]

  • 13. Establishment of a clonal strain of hepatoma cells which maintain in culture the five enzymes of the urea cycle.
    Richardson UI, Snodgrass PJ, Nuzum CT, Tashjian AH.
    J Cell Physiol; 1974 Feb; 83(1):141-9. PubMed ID: 4149774
    [No Abstract] [Full Text] [Related]

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

  • 15. Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase.
    Matsuda I, Arashima S, Nambu H, Takekoshi Y, Anakura M.
    Pediatrics; 1971 Oct; 48(4):595-600. PubMed ID: 5114747
    [No Abstract] [Full Text] [Related]

  • 16. A neonatal screening test for argininosuccinic acid lyase deficiency and other urea cycle disorders.
    Talbot HW, Sumlin AB, Naylor EW, Guthrie R.
    Pediatrics; 1982 Oct; 70(4):526-31. PubMed ID: 7122151
    [Abstract] [Full Text] [Related]

  • 17. Hyperammonaemia in 20 families. Biochemical and genetical survey, including investigations in 3 new families.
    Palmer T, Oberholzer VG, Burgess EA, Butler LJ, Levin B.
    Arch Dis Child; 1974 Jun; 49(6):443-9. PubMed ID: 4852321
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia.
    Tuchman M, Yudkoff M.
    Mol Genet Metab; 1999 Jan; 66(1):10-5. PubMed ID: 9973542
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 12.