BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 1244090)

  • 1. Tryptophan metabolism in nervous disease.
    Brune GG; Pflughaupt KW
    Acta Vitaminol Enzymol; 1975; 29(1-6):184-9. PubMed ID: 1244090
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Tryptophan tolerance test in children].
    Pham-Huu-Trung ; Boisse J; Attal C; Charpentier C; Lévy H; Mozziconacci P
    Ann Pediatr (Paris); 1964 Mar; 11(3):168-75. PubMed ID: 4228261
    [No Abstract]   [Full Text] [Related]  

  • 3. [Metabolism of tryptophan and its significance in pathology of childhood].
    Kniazev IuA; Vakhrusheva LL
    Pediatriia; 1972 Feb; 51(2):73-8. PubMed ID: 4260899
    [No Abstract]   [Full Text] [Related]  

  • 4. Interconversions of indolic acids by bacteria and rat tissue--possible relevance to Hartnup disorder.
    Smith HG; Smith WR; Jepson JB
    Clin Sci; 1968 Apr; 34(2):333-42. PubMed ID: 5653691
    [No Abstract]   [Full Text] [Related]  

  • 5. [Pathologic deviations of tryptophan metabolism and their biochemical examination].
    Dreux C
    Ann Biol Clin (Paris); 1968; 26(1):57-72. PubMed ID: 4231425
    [No Abstract]   [Full Text] [Related]  

  • 6. [Applied neurochemistry (author's transl)].
    Kanig K
    MMW Munch Med Wochenschr; 1977 Jul; 119(27):911-8. PubMed ID: 408620
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The effect of pyridoxine on tryptophan metabolism in phenylketonuria.
    Heeley AF
    Clin Sci; 1965 Dec; 29(3):465-73. PubMed ID: 5848701
    [No Abstract]   [Full Text] [Related]  

  • 8. [Tryptophan metabolism in infants with phenylketonuria].
    Bührdel P; Grimm U; Wässer S; Knapp A; Wulff K
    Padiatr Grenzgeb; 1982; 21(4):309-17. PubMed ID: 7177669
    [No Abstract]   [Full Text] [Related]  

  • 9. Spontaneous porphyria of the Long-evans cinnamon rat: an animal model of Wilson's disease.
    Nakayama K; Takasawa A; Terai I; Okui T; Ohyama T; Tamura M
    Arch Biochem Biophys; 2000 Mar; 375(2):240-50. PubMed ID: 10700380
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Clinical importance of tryptophan metabolism disorders].
    Korzon M; Korzon T
    Pol Tyg Lek; 1978 May; 33(19):783-6. PubMed ID: 351588
    [No Abstract]   [Full Text] [Related]  

  • 11. Hepatic alteration of tryptophan metabolism in an acute porphyria model Its relation with gluconeogenic blockage.
    Lelli SM; Mazzetti MB; San Martín de Viale LC
    Biochem Pharmacol; 2008 Feb; 75(3):704-12. PubMed ID: 17996218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tryptophan metabolism in untreated phenylketonuria.
    Kochen W; Bührlen E; Byrd DJ
    Acta Vitaminol Enzymol; 1975; 29(1-6):177-84. PubMed ID: 1244089
    [No Abstract]   [Full Text] [Related]  

  • 13. Tryptophan metabolism in a patient with phenylketonuria and scleroderma: a proposed explanation of the indole defect in phenylketonuria.
    Drummond KN; Michael AF; Good RA
    Can Med Assoc J; 1966 Apr; 94(16):834-8. PubMed ID: 5929533
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Intravenous heme-albumin in acute intermittent porphyria: evidence for repletion of hepatic hemoproteins and regulatory heme pools.
    Bonkovsky HL; Healey JF; Lourie AN; Gerron GG
    Am J Gastroenterol; 1991 Aug; 86(8):1050-6. PubMed ID: 1713408
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Hartnup disease].
    Berger R; Broyer M
    Presse Med (1893); 1968 Jan; 76(1):21-2. PubMed ID: 5637804
    [No Abstract]   [Full Text] [Related]  

  • 16. [L-tryptophan metabolism in phenylketonuria].
    Vassella F; Colombo JP; Humbel R; Rossi E
    Helv Paediatr Acta; 1968 Feb; 23(1):22-36. PubMed ID: 5688325
    [No Abstract]   [Full Text] [Related]  

  • 17. Disorders of intestinal transport of amino acids.
    Thier SO; Alpers DH
    Am J Dis Child; 1969 Jan; 117(1):13-23. PubMed ID: 4883974
    [No Abstract]   [Full Text] [Related]  

  • 18. [Chief clinical syndromes in children with tryptophan metabolism disorders (literature survey)].
    Tabolin VA; Kruglov BV; Lebedev VP; Levitina NO
    Vopr Okhr Materin Det; 1972 Jun; 17(6):45-8. PubMed ID: 4560708
    [No Abstract]   [Full Text] [Related]  

  • 19. Elevated brain tryptophan and enhanced 5-hydroxytryptamine turnover in acute hepatic heme deficiency: clinical implications.
    Litman DA; Correia MA
    J Pharmacol Exp Ther; 1985 Feb; 232(2):337-45. PubMed ID: 3968635
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Use of the stable isotope 65Cu test for the screening of Wilson's disease in a family with two affected members.
    Merli M; Patriarca M; Loudianos G; Valente C; Riggio O; De Felice G; Petrucci F; Caroli S; Attili AF
    Ital J Gastroenterol Hepatol; 1998 Jun; 30(3):270-5. PubMed ID: 9759594
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.