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

249 related items for PubMed ID: 7204885

  • 1. 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; 3(4):357-63. PubMed ID: 7204885
    [Abstract] [Full Text] [Related]

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

  • 3. [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]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 6. Newborn screening: the role of the obstetrician.
    Larsson A, Therrell BL.
    Clin Obstet Gynecol; 2002 Sep; 45(3):697-710; discussion 730-2. PubMed ID: 12370609
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Screening of congenital hypothyroidism, phenylketonuria, galactosemia, homocystinuria, and maple syrup urine disease in moderate to severe mentally retarded Chinese children.
    Hsiao KJ, Chen CH, Liu TT, Wu SJ, Plettner C, Clemens P.
    Taiwan Yi Xue Hui Za Zhi; 1989 Jan; 88(1):18-22. PubMed ID: 2787833
    [Abstract] [Full Text] [Related]

  • 9. Genetic screening of the newborn in Australia. Results for 1978.
    Pitt D, Connelly J, Francis I, Wilcken B, Brown DA, Hill G, Masters P, Tucker RG, Raby J, McFarlane J.
    Med J Aust; 1979 Sep 08; 2(5):272-3. PubMed ID: 514173
    [Abstract] [Full Text] [Related]

  • 10. Screening for metabolic disorders. How are we doing?
    Irons M.
    Pediatr Clin North Am; 1993 Oct 08; 40(5):1073-85. PubMed ID: 8414711
    [Abstract] [Full Text] [Related]

  • 11. Neonatal screening for congenital hypothyroidism and phenylketonuria at Siriraj Hospital, Mahidol University, Bangkok, Thailand--a pilot study.
    Wasant P, Liammongkolkul S, Srisawat C.
    Southeast Asian J Trop Med Public Health; 1999 Oct 08; 30 Suppl 2():33-7. PubMed ID: 11400774
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 14. Multiple positive results during a neonatal screening program: a retrospective analysis of incidence, clinical implications and outcomes.
    Zaffanello M, Maffeis C, Zamboni G.
    J Perinat Med; 2005 Oct 08; 33(3):246-51. PubMed ID: 15914349
    [Abstract] [Full Text] [Related]

  • 15. Newborn screening for PKU and congenital hypothyroidism in Latvia.
    Lugovska R, Vevere P, Andrusaite R, Kornejeva A.
    Southeast Asian J Trop Med Public Health; 1999 Oct 08; 30 Suppl 2():52-3. PubMed ID: 11400783
    [Abstract] [Full Text] [Related]

  • 16. [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]

  • 17. [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]

  • 18. The value of screening in paediatrics.
    Carter RA.
    J R Coll Physicians Lond; 1976 Jan 22; 10(2):153-60. PubMed ID: 54421
    [No Abstract] [Full Text] [Related]

  • 19. Rapid automated quantitation of isoleucine, leucine, tyrosine and phenylalanine from dried blood filter paper specimens.
    Qu Y, Miller JB, Slocum RH, Shapira E.
    Clin Chim Acta; 1991 Dec 16; 203(2-3):191-7. PubMed ID: 1777980
    [Abstract] [Full Text] [Related]

  • 20. Pediatric clinical aspects of aminoacidopathies.
    Hooft C, Carton D.
    Monogr Hum Genet; 1972 Dec 16; 6():50-63. PubMed ID: 4663915
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.