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 *

159 related articles for article (PubMed ID: 4593296)

  • 41. 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]  

  • 42. High-voltage electrophoresis in urinary amino acid screening.
    Holmgren G; Jeppson JO; Samuelson G
    Scand J Clin Lab Invest; 1970 Dec; 26(4):313-8. PubMed ID: 5486398
    [No Abstract]   [Full Text] [Related]  

  • 43. Diagnosis and treatment: interpreting the positive screening test in the newborn infant.
    Scriver CR
    Pediatrics; 1967 May; 39(5):764-8. PubMed ID: 6026878
    [No Abstract]   [Full Text] [Related]  

  • 44. [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]  

  • 45. 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]  

  • 46. MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
    COFFEY VP
    J Ir Med Assoc; 1964 Mar; 54():84-7. PubMed ID: 14130648
    [No Abstract]   [Full Text] [Related]  

  • 47. The dietary therapy of inherited metabolic disease.
    Snyderman SE
    Prog Food Nutr Sci; 1975; 1(7-8):507-30. PubMed ID: 57628
    [No Abstract]   [Full Text] [Related]  

  • 48. A survey of inborn errors of amino acid metabolism and transport in man.
    Wellner D; Meister A
    Annu Rev Biochem; 1981; 50():911-68. PubMed ID: 6791581
    [No Abstract]   [Full Text] [Related]  

  • 49. The child with an unusual odor. A clinical resumé.
    Mace JW; Goodman SI; Centerwall WR; Chinnock RF
    Clin Pediatr (Phila); 1976 Jan; 15(1):57-62. PubMed ID: 812627
    [No Abstract]   [Full Text] [Related]  

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

  • 51. [Diseases of newborn infants based on inborn anomalies of metabolism. 1. Theoretical principles].
    Plöchl E
    Wien Med Wochenschr; 1970 Oct; 120(41):707-11. PubMed ID: 4918107
    [No Abstract]   [Full Text] [Related]  

  • 52. [Phaenotypic aspects of hereditary aminoacidopathies (author's transl)].
    Becker K
    Monatsschr Kinderheilkd; 1981 Oct; 129(10):556-63. PubMed ID: 6801479
    [TBL] [Abstract][Full Text] [Related]  

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

  • 54. Thin-layer chromatographic screening of amino acids in plasma and urine of newborns.
    Century B; Vorkink WP; Natelson S
    Clin Chem; 1974 Nov; 20(11):1446-50. PubMed ID: 4417439
    [No Abstract]   [Full Text] [Related]  

  • 55. Inborn errors of metabolism associated with unusual odors.
    Carpenter DG; Carter CH
    J Fla Med Assoc; 1970 May; 57(5):31-3. PubMed ID: 5449191
    [No Abstract]   [Full Text] [Related]  

  • 56. 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]  

  • 57. [Test program for the earlydetection of inborn errors of metabolism].
    Thlhamer O
    Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):37-8. PubMed ID: 5398916
    [No Abstract]   [Full Text] [Related]  

  • 58. 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]  

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

  • 60. Detection of heterozygotes for phenylketonuria and hyperphenylaianinemia by gas-chromatographic analysis of aromatic acid excretion in urine.
    Koepp P; Hoffman B
    Clin Chim Acta; 1975 Feb; 58(3):215-21. PubMed ID: 1112063
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.