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 *

164 related articles for article (PubMed ID: 4609646)

  • 1. Neonatal screening for inborn errors of amino acid metabolism.
    Levy HL
    Clin Endocrinol Metab; 1974 Mar; 3(1):153-66. PubMed ID: 4609646
    [No Abstract]   [Full Text] [Related]  

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

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

  • 4. 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; 203(2-3):191-7. PubMed ID: 1777980
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. Isocratic reverse-phase liquid chromatography assay for amino acid metabolic disorders using eluates of dried blood spots.
    Vollmer DW; Jinks DC; Guthrie R
    Anal Biochem; 1990 Aug; 189(1):115-21. PubMed ID: 2278380
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. [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]  

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

  • 10. [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; 120(18):619-22. PubMed ID: 306535
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neonatal screening tests.
    Mamunes P
    Pediatr Clin North Am; 1980 Nov; 27(4):733-51. PubMed ID: 7005846
    [No Abstract]   [Full Text] [Related]  

  • 12. [5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report].
    Thalhammer O; Scheibenreiter S; Schön R; Knoll E; Schmierer G
    Wien Klin Wochenschr; 1972; 84():Suppl 2:3-12. PubMed ID: 5085466
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic screening.
    Levy HL
    Adv Hum Genet; 1973; 4():1-104. PubMed ID: 4593296
    [No Abstract]   [Full Text] [Related]  

  • 14. Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
    Levy HL; Barkin E
    J Lab Clin Med; 1971 Oct; 78(4):517-23. PubMed ID: 5114049
    [No Abstract]   [Full Text] [Related]  

  • 15. [Experiences with a new amino acid analyzer for a rapid analysis].
    Irtel von Brenndorff A; Hagge W
    Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):417-9. PubMed ID: 5523694
    [No Abstract]   [Full Text] [Related]  

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

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

  • 18. Screening for inherited metabolic disease by plasma chromatography (Scriver) in a large city.
    Raine DN; Cooke JR; Andrews WA; Mahon DF
    Br Med J; 1972 Jul; 3(5817):7-13. PubMed ID: 5039582
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Routine thin-layer-chromatography in 25000 newborn infants. Comparison with the Guthrie-tests].
    Schön R; Thalhammer O
    Z Kinderheilkd; 1971; 111(3):223-32. PubMed ID: 5157652
    [No Abstract]   [Full Text] [Related]  

  • 20. Hereditary disorders of amino acid metabolism associated with mental deficiency.
    Berry HK
    Ann N Y Acad Sci; 1969 Sep; 166(1):66-73. PubMed ID: 5262032
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.