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 *

102 related articles for article (PubMed ID: 6457308)

  • 1. [Biochemical changes in intra- and inter-metabolic syndromes].
    Pâtea P; Tănase-Mogos I; Petrescu L; Meilă P; Pesamosca A; Ursuleanu L; Toncescu N; Rădulescu G; Ulmeanu C
    Physiologie; 1981; 18(1):19-29. PubMed ID: 6457308
    [No Abstract]   [Full Text] [Related]  

  • 2. [Biochemical and clinical correlations in children suspected of having lysosomal diseases].
    Tănase-Mogos I; Turcanu L; Petrescu L; Popescu M
    Physiologie; 1981; 18(1):37-45. PubMed ID: 6794050
    [No Abstract]   [Full Text] [Related]  

  • 3. [Pathological metabolic products in the urine].
    Simon KH
    Med Monatsschr; 1969 Mar; 23(3):137-9. PubMed ID: 5779075
    [No Abstract]   [Full Text] [Related]  

  • 4. [Biochemistry of the blood and urine in members of families suspected of having hereditary metabolic defects].
    Tănase-Mogoş I; Petrescu L; Jemna M; Ankăr V; Feldioreanu E
    Physiologie; 1980; 17(2):101-11. PubMed ID: 6770382
    [No Abstract]   [Full Text] [Related]  

  • 5. Detection of metabolic disorders. Chromatographic procedures and interpretation of results.
    Berry HK; Leonard C; Peters H; Granger M; Chunekamrai N
    Clin Chem; 1968 Nov; 14(11):1033-65. PubMed ID: 4972564
    [No Abstract]   [Full Text] [Related]  

  • 6. [Simple screening tests for the detection of congenital metabolic disorders of amino acids, sugars, and mycopolysaccharides].
    Hyánek J
    Cas Lek Cesk; 1968 Nov; 107(47):1430-3. PubMed ID: 4235131
    [No Abstract]   [Full Text] [Related]  

  • 7. Screening for metabolic disorders using gas-liquid chromatography, mass spectrometry, and computer technique.
    Jellum E; Stokke O; Eldjarn L
    Scand J Clin Lab Invest; 1971 May; 27(3):273-85. PubMed ID: 4931892
    [No Abstract]   [Full Text] [Related]  

  • 8. [Biochemical differentiation of mucopolysaccharidoses].
    Spranger J; Wiedemann HR
    Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):421-3. PubMed ID: 4257110
    [No Abstract]   [Full Text] [Related]  

  • 9. [Importance of the culture of cells in vitro for the diagnosis and study of metabolic diseases].
    Esposito G
    Pediatria (Napoli); 1971; 79(2):270-83. PubMed ID: 4255382
    [No Abstract]   [Full Text] [Related]  

  • 10. Detection of inborn errors of metabolism.
    Boggs DE
    CRC Crit Rev Clin Lab Sci; 1971; 2(4):529-72. PubMed ID: 4257997
    [No Abstract]   [Full Text] [Related]  

  • 11. [Chromatography of amino acids on a thin layer of cellulose in urine exminations in inborn errors of metabolism].
    Hyánek J
    Cas Lek Cesk; 1969 Nov; 108(49):1479-81. PubMed ID: 5357423
    [No Abstract]   [Full Text] [Related]  

  • 12. Extra heating of amino acids.
    Henderson MJ; Allen JT; Holton JB; Goodall R
    Clin Chim Acta; 1985 Mar; 146(2-3):203-5. PubMed ID: 3987048
    [No Abstract]   [Full Text] [Related]  

  • 13. [Thin layer chromatography in clinical studies. IV. Separation of phosphoethanolamine].
    Dittmann J
    Z Klin Chem Klin Biochem; 1966 Jan; 4(1):10-1. PubMed ID: 5982669
    [No Abstract]   [Full Text] [Related]  

  • 14. Quality of analytical performance in inherited metabolic disorders: the role of ERNDIM.
    Fowler B; Burlina A; Kozich V; Vianey-Saban C
    J Inherit Metab Dis; 2008 Dec; 31(6):680-9. PubMed ID: 19016343
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Use of Toluidine Blue for sequential staining of urinary amino acid chromatograms.
    Curtis HT; Buist NR
    J Chromatogr; 1971 Apr; 57(1):165-6. PubMed ID: 4102684
    [No Abstract]   [Full Text] [Related]  

  • 16. Set of simple side-room urine tests for detection of inborn errors of metabolism.
    Buist NR
    Br Med J; 1968 Jun; 2(5607):745-9. PubMed ID: 4231911
    [No Abstract]   [Full Text] [Related]  

  • 17. Urinary metabolic screening in children with psycho-neurological diseases. Evaluation of different screening tests.
    Hambraeus L; Holmgren G
    Ups J Med Sci Suppl; 1974; 15():1-23. PubMed ID: 4274307
    [No Abstract]   [Full Text] [Related]  

  • 18. Inborn errors of metabolism in acutely sick children.
    Dhareshwar SS; Ambani LM; Suchak RH; Danthi V
    Indian J Med Res; 1982 Nov; 76():716-22. PubMed ID: 7166367
    [No Abstract]   [Full Text] [Related]  

  • 19. Proton MR spectroscopy of pediatric brain metabolic disorders.
    Wang ZJ; Zimmerman RA
    Neuroimaging Clin N Am; 1998 Nov; 8(4):781-807. PubMed ID: 9769342
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Quantitative UPLC-MS/MS analysis of underivatised amino acids in body fluids is a reliable tool for the diagnosis and follow-up of patients with inborn errors of metabolism.
    Waterval WA; Scheijen JL; Ortmans-Ploemen MM; Habets-van der Poel CD; Bierau J
    Clin Chim Acta; 2009 Sep; 407(1-2):36-42. PubMed ID: 19559691
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.