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

151 related items for PubMed ID: 4614217

  • 1. [Early diagnosis of phenylketonuria, homocystinuria and maple syrup urine disease in the GDR with the aid of Gatri's microbiological inhibitor test].
    Makhill G, Knapp A.
    Pediatriia; 1974 Dec; (12):27-30. PubMed ID: 4614217
    [No Abstract] [Full Text] [Related]

  • 2. [Results of screening studies for phenylketonuria, maple syrup disease and homocystinuria using Guthrie's test].
    Machill G.
    Kinderarztl Prax; 1973 May; 41(5):205-9. PubMed ID: 4732358
    [No Abstract] [Full Text] [Related]

  • 3. [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]

  • 4. [Screening of the Westphalia-Lippe newborns of 1977 for phenylketonuria, histidinemia, homocystinuria and maple syrup disease. Furthermore a pilot study of galactosemia and galactokinase deficiency disease].
    Menne F, Otte HJ, Krüger M, Winterhoff D.
    MMW Munch Med Wochenschr; 1979 Jun 22; 121(25):833-4. PubMed ID: 111089
    [No Abstract] [Full Text] [Related]

  • 5. [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]

  • 6. [Early diagnosis of hereditary metabolic diseases in the newborn by means of microbiological Guthrie tests].
    Schmid-Rüter E.
    Fortschr Med; 1978 Jun 22; 96(24):1289-93. PubMed ID: 96002
    [Abstract] [Full Text] [Related]

  • 7. Neonatal screening in Italy for congenital hypothyroidism and metabolic disorders: hyperphenylalaninemia, maple syrup urine disease and homocystinuria.
    Antonozzi I, Dominici R, Andreoli M, Monaco F.
    J Endocrinol Invest; 1980 Jun 22; 3(4):357-63. PubMed ID: 7204885
    [Abstract] [Full Text] [Related]

  • 8. [Hereditary amino acid metabolism disorders. Indications for early diagnosis].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):423-8. PubMed ID: 4680607
    [No Abstract] [Full Text] [Related]

  • 9. [Results of a nine-year phenylketonuria (PKU) screening (author's transl)].
    Menne F.
    MMW Munch Med Wochenschr; 1975 Jan 10; 117(2):63-8. PubMed ID: 164621
    [Abstract] [Full Text] [Related]

  • 10. Some inborn errors of metabolism.
    Barbor P.
    Nurs Mirror; 1978 Jul 20; 147(3):21-2. PubMed ID: 248774
    [No Abstract] [Full Text] [Related]

  • 11. [Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):430-1. PubMed ID: 4681731
    [No Abstract] [Full Text] [Related]

  • 12. [The early recognition of congenital metabolic diseases].
    Steuber W.
    Munch Med Wochenschr; 1971 Mar 26; 113(13):463-7. PubMed ID: 5108281
    [No Abstract] [Full Text] [Related]

  • 13. [Detection of congenital metabolic diseases with mental retardation].
    Colombo JP.
    Rev Otoneuroophtalmol; 1971 Nov 26; 43(7):328-33. PubMed ID: 5159706
    [No Abstract] [Full Text] [Related]

  • 14. Recent advances in the early detection and treatment of inborn errors with brain damage.
    Bickel H.
    Neuropadiatrie; 1969 Nov 26; 1(1):1-11. PubMed ID: 4942066
    [No Abstract] [Full Text] [Related]

  • 15. Pediatric clinical aspects of aminoacidopathies.
    Hooft C, Carton D.
    Monogr Hum Genet; 1972 Nov 26; 6():50-63. PubMed ID: 4663915
    [No Abstract] [Full Text] [Related]

  • 16. Recent developments in neonatal screening.
    Naylor EW.
    Semin Perinatol; 1985 Apr 26; 9(3):232-49. PubMed ID: 3832439
    [No Abstract] [Full Text] [Related]

  • 17. Diagnosis of disorders in amino acid methabolism by chemical ionization mass spectrometry.
    Issachar D, Yinon J.
    Clin Chim Acta; 1976 Dec 01; 73(2):307-14. PubMed ID: 1000850
    [Abstract] [Full Text] [Related]

  • 18. [Methodology of care for children with phenylketonuria and maple-syrup urine disease].
    Jiménez Soto Z.
    Arch Latinoam Nutr; 1993 Sep 01; 43(3):204-10. PubMed ID: 8779621
    [Abstract] [Full Text] [Related]

  • 19. [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]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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