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 *

166 related articles for article (PubMed ID: 5022447)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. [Detection of metabolic diseases].
    Adriaenssens K; Van Sande M
    Acta Neurol Psychiatr Belg; 1968 Oct; 68(10):719-28. PubMed ID: 4976725
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Metabolic disorders associated with mental retardation.
    Hsia DY; Berman JL; Justice P; Nadler HL; O'Flynn ME
    Pediatr Clin North Am; 1968 Nov; 15(4):889-904. PubMed ID: 4883204
    [No Abstract]   [Full Text] [Related]  

  • 11. [Early detection of congenital metabolic anomalies].
    Thalhammer O
    Klin Padiatr; 1973 Mar; 185(2):81-90. PubMed ID: 4576950
    [No Abstract]   [Full Text] [Related]  

  • 12. [A pilot study of selective screening for high risk children with inborn error of metabolism using tandem mass spectrometry in China].
    Gu XF; Han LS; Gao XL; Yan YL; Ye J; Qiu WJ
    Zhonghua Er Ke Za Zhi; 2004 Jun; 42(6):401-4. PubMed ID: 15265419
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic diagnostic studies for mental retardation.
    Beaudet AL
    Curr Probl Pediatr; 1978 Mar; 8(5):1-47. PubMed ID: 657833
    [No Abstract]   [Full Text] [Related]  

  • 14. [Screening for congenital metabolic diseases in mentally retarded patients in 6 psychiatric institutions of Lower Saxony].
    Byrd DJ; Brötling D; Brodehl J; Hunneman DH
    Klin Padiatr; 1984; 196(5):298-303. PubMed ID: 6492685
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A guide to screening newborn infants for inborn errors of metabolism.
    Buist NR; Jhaveri BM
    J Pediatr; 1973 Mar; 82(3):511-22. PubMed ID: 4266933
    [No Abstract]   [Full Text] [Related]  

  • 16. [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]  

  • 17. An evaluation of the gas chromatographic analysis of plasma amino acids.
    Pellizzari ED; Brown JH; Talbot P; Farmer RW; Fabre LF
    J Chromatogr; 1971 Mar; 55(2):281-9. PubMed ID: 5547798
    [No Abstract]   [Full Text] [Related]  

  • 18. Screening for biochemical abnormalities in the urine of the mentally handicapped in Dublin.
    Moore PT; Martin MC; Coffey VP
    J Ment Defic Res; 1972 Jun; 16(2):128-38. PubMed ID: 4277644
    [No Abstract]   [Full Text] [Related]  

  • 19. An approach to the diagnosis of overwhelming metabolic disease in early infancy.
    Nyhan WL
    Curr Probl Pediatr; 1977 Apr; ():1-20. PubMed ID: 856539
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.