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 *

107 related articles for article (PubMed ID: 3987048)

  • 1. 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]  

  • 2. Extra heating of TLC plates detects two lysosomal storage diseases, aspartylglucosaminuria and fucosidosis, during routine urinary amino acid screening.
    Simell O; Sipilä I; Autio S
    Clin Chim Acta; 1983 Sep; 133(2):227-32. PubMed ID: 6627685
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. Screening tests and chromatography for the detection of inborn errors of metabolism.
    Stuber A
    Clin Chim Acta; 1972 Feb; 36(2):309-13. PubMed ID: 5008795
    [No Abstract]   [Full Text] [Related]  

  • 5. Screening for metabolic disorders associated with mental retardation.
    Hill A; Zaleski WA
    Clin Biochem; 1972 Mar; 5(1):33-45. PubMed ID: 5022447
    [No Abstract]   [Full Text] [Related]  

  • 6. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.
    Yahya NA; Ismail Z; Embong KH; Mohamad SA
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():130-3. PubMed ID: 8629091
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Two-dimensional thin-layer chromatography on two-layer plates of amino acids.
    Kraffczyk F; Helger R; Lang H
    Clin Chem; 1970 Aug; 16(8):662-6. PubMed ID: 5474194
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. Thin-layer chromatography of amino acids in blood.
    Giguère R; Shapcott D; Lemieux B
    J Chromatogr; 1974 Jul; 95(1):122-6. PubMed ID: 4855191
    [No Abstract]   [Full Text] [Related]  

  • 11. Application of automation and systems analysis to detection of histidinemia.
    Newton DA; Summer GK; Hill HD; Salameh K
    Biochem Med; 1972 Oct; 6(5):397-408. PubMed ID: 4561695
    [No Abstract]   [Full Text] [Related]  

  • 12. Separation of amino acids in physiological fluids by two-dimensional thin-layer chromatography.
    White HH
    Clin Chim Acta; 1968 Sep; 21(3):297-302. PubMed ID: 5725187
    [No Abstract]   [Full Text] [Related]  

  • 13. Urinary glycosaminoglycans in aspartylglycosaminuria: evidence for disturbed proteoglycan metabolism.
    Näntö-Salonen K; Larjava H; Aalto M; Kivimäki T
    Clin Chim Acta; 1985 Mar; 146(2-3):111-8. PubMed ID: 3987044
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Vigabatrin--interference with urinary amino acid analysis.
    Preece MA; Sewell IJ; Taylor JA; Green A
    Clin Chim Acta; 1993 Sep; 218(1):113-6. PubMed ID: 8299214
    [No Abstract]   [Full Text] [Related]  

  • 15. [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]  

  • 16. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders].
    Khiari D; Tebib N; Kaabachi N; Ben Dridi MF; Mebazaa A
    Tunis Med; 1995 May; 73(5):159-67. PubMed ID: 9507277
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. An improved technique for the analysis of amino acids and related compounds on thin layers of cellulose. VI. The characterization of small peptides by thin-layer and ion-exchange chromatography.
    Heathcote JG; Washington RJ; Keogh BJ; Glanville RW
    J Chromatogr; 1972 Feb; 65(2):397-405. PubMed ID: 5016272
    [No Abstract]   [Full Text] [Related]  

  • 19. Screening for sulfite oxidase deficiency.
    Kutter D; Humbel R
    Clin Chim Acta; 1969 May; 24(2):211-4. PubMed ID: 5787324
    [No Abstract]   [Full Text] [Related]  

  • 20. Chromatographic analysis of amino and organic acids in physiological fluids to detect inborn errors of metabolism.
    Woontner M; Goodman SI
    Curr Protoc Hum Genet; 2006 Nov; Chapter 17():Unit 17.2. PubMed ID: 18428392
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.