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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 4041281)

  • 1. Chromatographic screening of 70,328 neonates for inborn errors of amino acid metabolism.
    Méhes K; Juhász E; Ruszinkó V
    Acta Paediatr Hung; 1985; 26(2):147-9. PubMed ID: 4041281
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Newborn mass-screening programme for histidinaemia: increased efficiency through selective thin-layer chromatography (author's transl)].
    Schön R
    Wien Klin Wochenschr; 1977 May; 89(10):353-5. PubMed ID: 868031
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Mass screening for histidinaemia:rationalization by selective thin layer chromatography. First results].
    Ergebnisse E
    Monatsschr Kinderheilkd (1902); 1976 Sep; 129(9):639-42. PubMed ID: 979981
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inborn errors of amino acid metabolism in north India.
    Kaur M; Das GP; Verma IC
    J Inherit Metab Dis; 1994; 17(2):230-3. PubMed ID: 7967478
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Histidinaemia in Sweden. Report on a neonatal screening programme.
    Alm J; Holmgren G; Larsson A; Schimpfessel L
    Clin Genet; 1981 Sep; 20(3):229-33. PubMed ID: 7307322
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Areas of applicability of thin-layer chromatography. Practical mass screening; data on intestinal mucosa lesions].
    Szabó B
    Padiatr Padol; 1983; 18(2):105-11. PubMed ID: 6856315
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Routine screening for inborn errors using urine filterpaper specimens at age 4-5 weeks (author's transl)].
    Schön R; Thalhammer O
    Padiatr Padol; 1976; 11(1):319-25. PubMed ID: 1250631
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Screening for hyperaminoacidemias in newborns by thin-layer chromatography on DEAE-cellulose.
    Vercaemst R; Blaton V; Lievens-Taveirne J; Peeters H
    Acta Paediatr Belg; 1973; 27(5):334-47. PubMed ID: 4779694
    [No Abstract]   [Full Text] [Related]  

  • 9. Massachusetts metabolic disorders screening program. I. Technics and results of urine screening.
    Levy HL; Madigan PM; Shih VE
    Pediatrics; 1972 Jun; 49(6):825-36. PubMed ID: 5041315
    [No Abstract]   [Full Text] [Related]  

  • 10. Ion-exchange thin-layer chromatographic screening test for phenylketonuria and other aminoacidaemias.
    Kovács J
    Acta Paediatr Acad Sci Hung; 1973; 14(3):165-9. PubMed ID: 4785695
    [No Abstract]   [Full Text] [Related]  

  • 11. A ten-year follow-up study of urinary screening for inherited metabolic disorders.
    Hyánek J; Viletová H; Kunová V; Záková L; Kubík M; Matousová M
    Czech Med; 1987; 10(2):64-9. PubMed ID: 3115737
    [TBL] [Abstract][Full Text] [Related]  

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

  • 13. Plasma amino acid screening in the newborn.
    Mellon J
    Arch Dis Child; 1971 Dec; 46(250):882. PubMed ID: 5129204
    [No Abstract]   [Full Text] [Related]  

  • 14. Newborn screening of urea cycle disorders.
    Naylor EW
    Pediatrics; 1981 Sep; 68(3):453-7. PubMed ID: 7279482
    [No Abstract]   [Full Text] [Related]  

  • 15. [A routine method for thin layer chromatographic determination of urocanic acid in blood samples impregnated on filter paper cards (author's transl)].
    Schön R
    J Clin Chem Clin Biochem; 1976 Oct; 14(10):501-2. PubMed ID: 993736
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Thin layer chromatography studies of capillary blood in newborn infants. Evaluation of utility for mass screening].
    Coradello H
    Klin Padiatr; 1972 Sep; 184(5):358-66. PubMed ID: 4673723
    [No Abstract]   [Full Text] [Related]  

  • 17. [Mass screening of genetic metabolic abnormalities with special reference to amino acid metabolism disorders, using chemical methods].
    Lubs H; Knapp A
    Z Arztl Fortbild (Jena); 1970 May; 64(10):516-9. PubMed ID: 5520559
    [No Abstract]   [Full Text] [Related]  

  • 18. Screening for inborn errors of amino acid metabolism.
    Wu JT
    Ann Clin Lab Sci; 1991; 21(2):123-42. PubMed ID: 2029175
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A neonatal screening test for argininosuccinic acid lyase deficiency and other urea cycle disorders.
    Talbot HW; Sumlin AB; Naylor EW; Guthrie R
    Pediatrics; 1982 Oct; 70(4):526-31. PubMed ID: 7122151
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Aminoaciduria screening in newborn infants using, comparatively, chromatographic and colorimetric methods].
    Pedrazzi AH; Rossi AR
    Rev Farm Bioquim Univ Sao Paulo; 1976; 14(2):241-54. PubMed ID: 1030516
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.