BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 14246093)

  • 21. Biochemical research in two cases of endogenous pellagra.
    Voiculescu V; Luca N; Hategan D
    Eur Neurol; 1973; 10(4):205-14. PubMed ID: 4778379
    [No Abstract]   [Full Text] [Related]  

  • 22. ACUTE CEREBELLAR ATAXIA ASSOCIATED WITH SOME FEATURES OF THE HARTNUP SYNDROME. PRESENTATION OF A CASE.
    FOIS A; LECCHINI L
    Helv Paediatr Acta; 1964 Jun; 19():42-9. PubMed ID: 14189842
    [No Abstract]   [Full Text] [Related]  

  • 23. Hereditary abnormalities of intestinal absorption.
    Milne MD
    Br Med Bull; 1967 Sep; 23(3):279-84. PubMed ID: 4865986
    [No Abstract]   [Full Text] [Related]  

  • 24. INVESTIGATION OF NEPHROCALCINOSIS AND NEPHROLITHIASIS.
    FOURMAN P
    J Clin Pathol; 1965 Jul; 18():568-71. PubMed ID: 14318720
    [No Abstract]   [Full Text] [Related]  

  • 25. [THE BIOCHEMICAL EFFECTS OF CERTAIN CHROMOSOMES].
    JEROME H
    Ann Genet; 1964; 7():88-100. PubMed ID: 14249004
    [No Abstract]   [Full Text] [Related]  

  • 26. [Chief clinical syndromes in children with tryptophan metabolism disorders (literature survey)].
    Tabolin VA; Kruglov BV; Lebedev VP; Levitina NO
    Vopr Okhr Materin Det; 1972 Jun; 17(6):45-8. PubMed ID: 4560708
    [No Abstract]   [Full Text] [Related]  

  • 27. INDOLYLACROYL GLYCINE EXCRETION IN A FAMILY WITH MENTAL RETARDATION.
    MELLMAN WJ; BARNESS LA; TEDESCO TA; BESSELMAN D
    Clin Chim Acta; 1963 Nov; 8():843-7. PubMed ID: 14089554
    [No Abstract]   [Full Text] [Related]  

  • 28. [Blue diaper syndrome].
    Takita H
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):574-5. PubMed ID: 9645138
    [No Abstract]   [Full Text] [Related]  

  • 29. Detection of inborn errors of metabolism in 1,117 patients studied because of suspected inherited disease.
    Vaca G; Hernández A; Ibarra B; Velázquez A; Olivares N; Sanchez-Corona J; Medina C; Cantú JM
    Arch Invest Med (Mex); 1981; 12(3):341-8. PubMed ID: 7294941
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Diagnostic methods for the detection of amino acid metabolism disorders].
    Lutz P
    Monatsschr Kinderheilkd (1902); 1973 May; 121(5):184-9. PubMed ID: 4197345
    [No Abstract]   [Full Text] [Related]  

  • 31. HYPERGLYCINEMIA. V. THE MISCIBLE POOL AND TURNOVER RATE OF GLYCINE AND THE FORMATION OF SERINE.
    NYHAN WL; CHILDS B
    J Clin Invest; 1964 Dec; 43(12):2404-9. PubMed ID: 14234837
    [No Abstract]   [Full Text] [Related]  

  • 32. THE DETERMINATION OF BETA-AMINO-ISOBUTYRIC ACID IN URINE.
    SMITH H; DYMOND B
    Clin Chim Acta; 1963 Jul; 8():614-20. PubMed ID: 14063978
    [No Abstract]   [Full Text] [Related]  

  • 33. Chromatographic study of "Reigelhaupt" chromogens in urine.
    YUWILER A; GOOD MH
    J Psychiatr Res; 1962 Dec; 1():215-27. PubMed ID: 14002926
    [No Abstract]   [Full Text] [Related]  

  • 34. PYRIDOXINE AND INFANTILE MYOCLONIC SEIZURES.
    FRENCH JH; GRUETER BB; DRUCKMAN R; O'BRIEN D
    Neurology; 1965 Feb; 15():101-13. PubMed ID: 14275268
    [No Abstract]   [Full Text] [Related]  

  • 35. [CRITICAL DISCUSSION ON A CASE OF NEPHROCALCINOSIS (ATYPICAL BURNETT'S SYNDROME)].
    KISSEL P; RAUBER G; DUREUX JB; SCHMITT J; PETIT J; DUC M
    Ann Med Nancy; 1964 Jan; 3():71-6. PubMed ID: 14136379
    [No Abstract]   [Full Text] [Related]  

  • 36. Familial protein intolerance. Possible nature of enzyme defect.
    Malmquist J; Jagenburg R; Lindstedt G
    N Engl J Med; 1971 May; 284(18):997-1002. PubMed ID: 5553484
    [No Abstract]   [Full Text] [Related]  

  • 37. [Amino acid metabolism and childhood pathology].
    Netakhata ZhN; Liapun SN
    Pediatriia; 1970; 49(12):63-73. PubMed ID: 4950145
    [No Abstract]   [Full Text] [Related]  

  • 38. [Hereditary digestive enzyme defects].
    Rey J
    Med Chir Dig; 1972; 1(1):41-4 contd. PubMed ID: 5054004
    [No Abstract]   [Full Text] [Related]  

  • 39. [TESTS FOR AMINO ACIDS IN URINE].
    SANO I; KAKIMOTO T
    No To Shinkei; 1964 Oct; 16():868-72. PubMed ID: 14220108
    [No Abstract]   [Full Text] [Related]  

  • 40. [THE CLINICAL FORM OF HARTNUP'S DISEASE].
    DEMEULEMEESTER F
    Acta Paediatr Belg; 1963; 17():215-22. PubMed ID: 14107571
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.