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 *

109 related articles for article (PubMed ID: 890978)

  • 1. [Determination of urinary alpha-keto-gamma-methylthiobutyric acid in hypermethionemia by use of gas chromatography and flame photometry (author's transl)].
    Favier A; Caillat D
    Clin Chim Acta; 1977 Sep; 79(2):419-23. PubMed ID: 890978
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sulfur-containing amino acids in the plasma and urine of homocystinurics.
    Perry TL; Hansen S; MacDougall L; Warrington PD
    Clin Chim Acta; 1967 Mar; 15(3):409-20. PubMed ID: 6034417
    [No Abstract]   [Full Text] [Related]  

  • 3. The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria.
    Faull KF; Bolton PD; Halpern B; Hammond J; Danks DM
    Clin Chim Acta; 1976 Dec; 73(3):553-9. PubMed ID: 1000872
    [No Abstract]   [Full Text] [Related]  

  • 4. Determination of sulphur amino acids by gas chromatography with flame photometric detection.
    Kataoka H; Tanaka H; Fujimoto A; Noguchi I; Makita M
    Biomed Chromatogr; 1994; 8(3):119-24. PubMed ID: 8075520
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The identification of tiglylglycine in the urine of a child with -methylcrotonylglycinuria.
    Gompertz D; Draffan GH
    Clin Chim Acta; 1972 Mar; 37():405-10. PubMed ID: 5022104
    [No Abstract]   [Full Text] [Related]  

  • 6. Aminoaciduria in a homocystinuric family.
    Kelly S; Copeland W; Leikhim E
    Clin Chim Acta; 1969 Dec; 26(3):586-7. PubMed ID: 5358562
    [No Abstract]   [Full Text] [Related]  

  • 7. Determination of branched chain amino acids, methionine, phenylalanine, tyrosine and alpha-keto acids in plasma and dried blood samples using HPLC with fluorescence detection.
    Kand'ár R; Záková P; Jirosová J; Sladká M
    Clin Chem Lab Med; 2009; 47(5):565-72. PubMed ID: 19290779
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cystathioninuria and homocystinuria.
    Levy HL; Mudd SH; Uhlendorf BW; Madigan PM
    Clin Chim Acta; 1975 Jan; 58(1):51-9. PubMed ID: 1122632
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Homocystinuria: metabolism of [35S]methionine.
    Brenton DP; Cusworth DC
    Clin Sci; 1966 Oct; 31(2):197-206. PubMed ID: 5955721
    [No Abstract]   [Full Text] [Related]  

  • 10. An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis.
    Daum RS; Scriver CR; Mamer OA; Delvin E; Lamm P; Goldman H
    Pediatr Res; 1973 Mar; 7(3):149-60. PubMed ID: 4690360
    [No Abstract]   [Full Text] [Related]  

  • 11. Spectrum of hypermethioninemia in neonatal screening.
    Chien YH; Chiang SC; Huang A; Hwu WL
    Early Hum Dev; 2005 Jun; 81(6):529-33. PubMed ID: 15935930
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 'Homocystinuria' and urinary excretion of beta-amino acids in patients treated with 6-azauridine.
    Hyánek J; Bremer HJ; Slavik M
    Clin Chim Acta; 1969 Aug; 25(2):288-90. PubMed ID: 5801395
    [No Abstract]   [Full Text] [Related]  

  • 13. Defect in alpha-ketobutyrate metabolism: a new inborn error.
    Yang W; Roth KS
    Clin Chim Acta; 1985 Jan; 145(2):173-82. PubMed ID: 3918815
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Primary cystathioninuria. Methionine load tests and response to pyridoxine.
    Bremer HJ; Endres W
    Helv Paediatr Acta; 1972 Nov; 27(5):525-36. PubMed ID: 4640904
    [No Abstract]   [Full Text] [Related]  

  • 15. Hypermethioninemias of genetic and non-genetic origin: A review.
    Mudd SH
    Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):3-32. PubMed ID: 21308989
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hypermethioninemia with other hyperaminoacidemias. Studies in infants on high-protein diets.
    Levy HL; Shih VE; Madigan PM; Karolkewicz V; Carr JR; Lum A; Richards AA; Crawford JD; MacCready RA
    Am J Dis Child; 1969 Jan; 117(1):96-103. PubMed ID: 5812761
    [No Abstract]   [Full Text] [Related]  

  • 17. Cholestasis and hypermethioninemia during dietary management of hereditary tyrosinemia type 1.
    Ameen VZ; Powell GK; Rassin DK
    J Pediatr; 1986 Jun; 108(6):949-52. PubMed ID: 2872285
    [No Abstract]   [Full Text] [Related]  

  • 18. 3-methyl-3-butenoic acid: an artefact in the urinary metabolic pattern of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
    Jakobs C; Bojasch M; Duran M; Ketting D; Wadman SK; Leupold D
    Clin Chim Acta; 1980 Sep; 106(1):85-9. PubMed ID: 6157502
    [No Abstract]   [Full Text] [Related]  

  • 19. A new type of hypermethioninemia in neonates.
    Tsuchiyama A; Oyanagi K; Nakata F; Uetsuji N; Tsugawa S; Nakao T; Mori M
    Tohoku J Exp Med; 1982 Nov; 138(3):281-8. PubMed ID: 7157356
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Methionine adenosyltransferase deficiency: new enzymatic defect associated with hypermethioninemia.
    Gaull GE; Tallan HH
    Science; 1974 Oct; 186(4158):59-60. PubMed ID: 4421454
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.