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

143 related items for PubMed ID: 5054004

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

  • 2. [Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer].
    Boisse J, Moatti N.
    Ann Biol Clin (Paris); 1973; 31(4):249-55. PubMed ID: 4579284
    [No Abstract] [Full Text] [Related]

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

  • 4. [The inborn errors of metabolism of amino acids].
    Tomaszewski L.
    Postepy Biochem; 1973; 19(1):91-122. PubMed ID: 4697972
    [No Abstract] [Full Text] [Related]

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

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

  • 7. [Malabsorption in hereditary disorders of the carbohydrate and amino acid metabolism].
    Linneweh F.
    Acta Paediatr Acad Sci Hung; 1969; 10(1):1-12. PubMed ID: 5793288
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. [Defects of renal tubular transport systems for amino acids].
    Gerok W.
    Med Klin; 1975 Feb 21; 70(8):301-12. PubMed ID: 1091836
    [No Abstract] [Full Text] [Related]

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

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

  • 12. [Inherited amino acid transport disorders].
    Igarashi Y, Tada K.
    Nihon Rinsho; 1992 Jul 21; 50(7):1587-92. PubMed ID: 1404888
    [Abstract] [Full Text] [Related]

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

  • 14. Inborn errors of metabolism associated with unusual odors.
    Carpenter DG, Carter CH.
    J Fla Med Assoc; 1970 May 21; 57(5):31-3. PubMed ID: 5449191
    [No Abstract] [Full Text] [Related]

  • 15. Inherited disorders of amino acid transport in relation to the kidney.
    Buehler BA.
    Ann Clin Lab Sci; 1981 May 21; 11(3):274-8. PubMed ID: 7018372
    [Abstract] [Full Text] [Related]

  • 16. Further investigations in the methionine malabsorption syndrome.
    Hooft C, Carton D, Snoeck J, Timmermans J, Antener I, van den Hende C.
    Helv Paediatr Acta; 1968 Aug 21; 23(4):334-49. PubMed ID: 5678411
    [No Abstract] [Full Text] [Related]

  • 17. [Intestinal enzymopathies of children (author's transl)].
    Schreier K.
    MMW Munch Med Wochenschr; 1976 Dec 24; 118(52-53):1695-1702. PubMed ID: 827699
    [Abstract] [Full Text] [Related]

  • 18. [Intestinal malabsorption and genetic defects].
    Porto JA, Mello Sda S, Junqueira A.
    Arq Bras Endocrinol Metabol; 1969 Apr 24; 18(1):5-23. PubMed ID: 5403667
    [No Abstract] [Full Text] [Related]

  • 19. Beta-apoprotein sufficiency and function.
    Gotto AM.
    N Engl J Med; 1969 Jun 05; 280(23):1297-8. PubMed ID: 5770055
    [No Abstract] [Full Text] [Related]

  • 20. [Idiopathic disorder of intestinal fat transport (Anderson's disease). A further case].
    Rey J, Jos J, Rey F, Leporrier M, Dechaux M, Ramon J, Frézal J.
    Arch Fr Pediatr; 1973 May 05; 30(5):564-5. PubMed ID: 4733664
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.