BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 413127)

  • 1. ["Atypical" metabolic forms of phenylketonuria (PKU) and leucinosis detected in newborn infants].
    Tănase I; Ciortoloman H; Popescu M; Grigorescu G; Ankăr V
    Physiologie; 1977; 14(4):257-61. PubMed ID: 413127
    [No Abstract]   [Full Text] [Related]  

  • 2. Family with intermittent maple syrup urine disease.
    Valman HB; Patrick AD; Seakins JW; Platt JW; Gompertz D
    Arch Dis Child; 1973 Mar; 48(3):225-8. PubMed ID: 4693464
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening of organic acids in urine by chemical ionization mass spectrometry.
    Issachar D; Yinon J
    Biomed Mass Spectrom; 1979 Feb; 6(2):47-56. PubMed ID: 420910
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diagnosis of disorders in amino acid methabolism by chemical ionization mass spectrometry.
    Issachar D; Yinon J
    Clin Chim Acta; 1976 Dec; 73(2):307-14. PubMed ID: 1000850
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recent work on phenylketonuria and maple syrup urine disease (leucinosis).
    WOOLF LI
    Proc R Soc Med; 1962 Oct; 55(10):824-6. PubMed ID: 14001839
    [No Abstract]   [Full Text] [Related]  

  • 6. A variant form of branched-chain keto aciduria.
    van der Horst JL; Wadman SK
    Acta Paediatr Scand; 1971 Sep; 60(5):594-9. PubMed ID: 5125167
    [No Abstract]   [Full Text] [Related]  

  • 7. [Early diagnosis of phenylketonuria, homocystinuria and maple syrup urine disease in the GDR with the aid of Gatri's microbiological inhibitor test].
    Makhill G; Knapp A
    Pediatriia; 1974 Dec; (12):27-30. PubMed ID: 4614217
    [No Abstract]   [Full Text] [Related]  

  • 8. Maple syrup urine disease (branched-chain keto-aciduria) variant type manifesting as hyperkinetic behaviour and mental retardation. Report of two cases.
    Kalyanaraman K; Chamukuttan S; Arjundas G; Gajanan N; Ramamurthi B
    J Neurol Sci; 1972 Feb; 15(2):209-17. PubMed ID: 5010106
    [No Abstract]   [Full Text] [Related]  

  • 9. [Methodology of care for children with phenylketonuria and maple-syrup urine disease].
    Jiménez Soto Z
    Arch Latinoam Nutr; 1993 Sep; 43(3):204-10. PubMed ID: 8779621
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Simultaneous retention index analysis of urinary amino acids and carboxylic acids for graphic recognition of abnormal state.
    Paik MJ; Lee HJ; Kim KR
    J Chromatogr B Analyt Technol Biomed Life Sci; 2005 Jul; 821(1):94-104. PubMed ID: 15894518
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Lists of food exchanges for use in phenylketonuria and maple-syrup urine disease].
    Jiménez Soto Z
    Arch Latinoam Nutr; 1993 Sep; 43(3):211-6. PubMed ID: 8779622
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ENZYMES IN MENTAL RETARDATION.
    ROSANOVA AR; NEIMEYER H; COMPALL T; MICHAELSON AS
    IMJ Ill Med J; 1964 Jul; 126():52-6. PubMed ID: 14183323
    [No Abstract]   [Full Text] [Related]  

  • 13. [Maple syrup urine disease: report of a mild variant case and results of dietary treatment].
    Stoppoloni G; Santinelli R; Prisco F; Tolone C; D'Ambrosio M
    Pediatria (Napoli); 1978 Sep; 86(3):409-20. PubMed ID: 754161
    [No Abstract]   [Full Text] [Related]  

  • 14. Prepurification and derivatization of alpha-keto acids using hydrazide gel. Application in gas chromatography and gas chromatography--mass spectrometry.
    Todoriki H; Hayashi T; Naruse H; Ikeda S
    J Chromatogr; 1982 Nov; 232(2):394-9. PubMed ID: 6818241
    [No Abstract]   [Full Text] [Related]  

  • 15. Transaminations between amino acids and keto acids elevated in phenylketonuria and maple syrup urine disease.
    Lees GJ; Weiner N
    J Neurochem; 1973 Feb; 20(2):389-403. PubMed ID: 4698286
    [No Abstract]   [Full Text] [Related]  

  • 16. Profiles of urinary volatiles from metabolic disorders characterized by unusual odors.
    Burke DG; Halpern B; Malegan D; McCairns E; Danks D; Schlesinger P; Wilken B
    Clin Chem; 1983 Oct; 29(10):1834-8. PubMed ID: 6616835
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Screening newborn infants for phenylketonuria, histadinemia, homocystinuria and maple syrup disease. Results from north rhein-westphalia (1974-1976) (author's transl].
    Menne F; Otte HJ; Krüger M; Winterhoff D
    MMW Munch Med Wochenschr; 1978 May; 120(18):619-22. PubMed ID: 306535
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and biochemical observations on an apparently nonfatal variant of branched-chain ketoaciduria (maple syrup urine disease).
    MORRIS MD; LEWIS BD; DOOLAN PD; HARPER HA
    Pediatrics; 1961 Dec; 28():918-23. PubMed ID: 14476272
    [No Abstract]   [Full Text] [Related]  

  • 19. Urinary excretion of N-acetyl amino acids in patients with some inborn errors of amino acid metabolism.
    Jellum E; Horn L; Thoresen O; Kvittingen EA; Stokke O
    Scand J Clin Lab Invest Suppl; 1986; 184():21-6. PubMed ID: 3473611
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neuropathological observations in maple syrup urine disease: branched-chain ketoaciduria.
    SILBERMAN J; DANCIS J; FEIGIN I
    Arch Neurol; 1961 Oct; 5():351-63. PubMed ID: 13912814
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.