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

155 related items for PubMed ID: 4593296

  • 21. Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
    World Health Organ Tech Rep Ser; 1968; 401():1-57. PubMed ID: 4973455
    [No Abstract] [Full Text] [Related]

  • 22. Disorders of intestinal transport of amino acids.
    Thier SO, Alpers DH.
    Am J Dis Child; 1969 Jan; 117(1):13-23. PubMed ID: 4883974
    [No Abstract] [Full Text] [Related]

  • 23. [Simultaneous thin-layer chromatography of blood and urine samples for the diagnosis of hereditary amino acid metabolism disorders].
    Peters WH, Lubs H, Knapp A.
    Z Arztl Fortbild (Jena); 1974 Jul 15; 68(14):716-25. PubMed ID: 4216183
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. [Neonatal diagnosis of hereditary metabolic diseases].
    Lambotte C.
    Rev Med Liege; 1973 Dec 15; 28(24):837-51. PubMed ID: 4769974
    [No Abstract] [Full Text] [Related]

  • 32. [Metabolic disorders, their early diagnosis and therapy in newborn infants].
    Tabolin VA.
    Vestn Akad Med Nauk SSSR; 1973 Dec 15; 28(6):76-86. PubMed ID: 4729650
    [No Abstract] [Full Text] [Related]

  • 33. [A screening test for phenylketonuria using a paper chromatography method].
    Halvorsen S, Skjelkvåle L.
    Lakartidningen; 1974 Mar 20; 71(12):1166-7. PubMed ID: 4821497
    [No Abstract] [Full Text] [Related]

  • 34. Screening for metabolic disorders. How are we doing?
    Irons M.
    Pediatr Clin North Am; 1993 Oct 20; 40(5):1073-85. PubMed ID: 8414711
    [Abstract] [Full Text] [Related]

  • 35. [Methods and results of screening newborn infants for aminoacidopathies].
    Bickel H.
    Monatsschr Kinderheilkd (1902); 1976 Sep 20; 129(9):650-3. PubMed ID: 979984
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Screening for inborn errors of metabolism in infancy.
    Hudson FP.
    Nurs Mirror Midwives J; 1975 Aug 28; 141(9):64-6. PubMed ID: 1041391
    [No Abstract] [Full Text] [Related]

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