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

987 related items for PubMed ID: 5085466

  • 21. [Screening and therapy of 6 metabolic diseases of hereditary nature which are possible causes of mental retardation: screening of 1,900,000 newborn infants since the year 1965].
    Menne F.
    Clin Ter; 1979 Mar 15; 88(5):445-59. PubMed ID: 466967
    [No Abstract] [Full Text] [Related]

  • 22. [Diet therapy of some inborn errors of metabolism].
    Perrone L.
    Pediatria (Napoli); 1974 Sep 30; 82(2):260-97. PubMed ID: 4473102
    [No Abstract] [Full Text] [Related]

  • 23. [25 years Austrian screening program for inborn errors of metabolism at the Vienna University].
    Widhalm K.
    Wien Klin Wochenschr; 1992 Sep 30; 104(16):510-3. PubMed ID: 1413809
    [Abstract] [Full Text] [Related]

  • 24. Newborn screening for hereditary metabolic disorders in Manitoba, 1965-1970.
    Fox JG, Hall DL, Haworth JC, Maniar A, Sekla L.
    Can Med Assoc J; 1971 Jun 19; 104(12):1085-8. PubMed ID: 5580751
    [Abstract] [Full Text] [Related]

  • 25. State screening for metabolic disorders in newborns.
    Stevens MB, Rigilano JC, Wilson CC.
    Am Fam Physician; 1988 Apr 19; 37(4):223-8. PubMed ID: 3358346
    [Abstract] [Full Text] [Related]

  • 26. [Screening newborn infants for phenylketonuria, histadinemia, homocystinuria and maple syrup disease. Results from north rhein-westphalia (1974-1976) (author's transl].
    Menne F, Otte HJ, Krüger M, Winterhoff D.
    MMW Munch Med Wochenschr; 1978 May 05; 120(18):619-22. PubMed ID: 306535
    [Abstract] [Full Text] [Related]

  • 27. [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]

  • 28. Dietary restriction in inborn errors of amino acid metabolism.
    Bickel H.
    Curr Concepts Nutr; 1979 Jul 15; 8():35-53. PubMed ID: 527358
    [No Abstract] [Full Text] [Related]

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

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

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Neonatal screening for metabolic and endocrine diseases.
    Tiwary CM.
    Nurse Pract; 1987 Sep 15; 12(9):28-35, 38, 41. PubMed ID: 3118277
    [Abstract] [Full Text] [Related]

  • 35. [Early diagnosis of congenital metabolic diseases].
    Steuer W.
    Minerva Med; 1971 Nov 03; 62(83):4047-52. PubMed ID: 5134399
    [No Abstract] [Full Text] [Related]

  • 36. [Screening for congenital metabolic disorders].
    Knapp A, Machill G.
    Kinderarztl Prax; 1974 Jun 03; 42(6):270-7. PubMed ID: 4610264
    [No Abstract] [Full Text] [Related]

  • 37. Phenylketonuria and other disorders of amino acid metabolism.
    Ampola MG.
    Pediatr Clin North Am; 1973 May 03; 20(2):507-36. PubMed ID: 4573597
    [No Abstract] [Full Text] [Related]

  • 38. [Early detection of hereditary metabolic diseases (author's transl)].
    Steuer W.
    Offentl Gesundheitswes; 1980 Dec 03; 42(12):949-54. PubMed ID: 6451829
    [No Abstract] [Full Text] [Related]

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

  • 40. [Detection of congenital metabolic diseases with mental retardation].
    Colombo JP.
    Rev Otoneuroophtalmol; 1971 Nov 03; 43(7):328-33. PubMed ID: 5159706
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 50.