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 *

125 related articles for article (PubMed ID: 6547653)

  • 1. Computer model of the metabolism of phenylalanine in normal subjects and in patients with phenylketonuria.
    Hjelm M; Kitney R; Lindsey P; Seakins J
    Comput Programs Biomed; 1984; 18(1-2):21-31. PubMed ID: 6547653
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Blood-brain barrier transport of amino acids in healthy controls and in patients with phenylketonuria.
    Knudsen GM; Hasselbalch S; Toft PB; Christensen E; Paulson OB; Lou H
    J Inherit Metab Dis; 1995; 18(6):653-64. PubMed ID: 8750601
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A model of human phenylalanine metabolism in normal subjects and in phenylketonuric patients.
    Kaufman S
    Proc Natl Acad Sci U S A; 1999 Mar; 96(6):3160-4. PubMed ID: 10077654
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria.
    Langenbeck U; Behbehani A; Mench-Hoinowski A
    J Inherit Metab Dis; 1992; 15(1):136-44. PubMed ID: 1583868
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Statistical properties of the Michaelis-Menten equation and their implication for inborn errors of metabolism.
    Seakins JW; Hjelm M; Wang KJ
    J Inherit Metab Dis; 1992; 15(3):431-4. PubMed ID: 1405486
    [No Abstract]   [Full Text] [Related]  

  • 6. In vivo proton magnetic resonance spectroscopy in phenylketonuria.
    Möller HE; Ullrich K; Weglage J
    Eur J Pediatr; 2000 Oct; 159 Suppl 2():S121-5. PubMed ID: 11043158
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenylalanine metabolites in phenylketonuria.
    Clemens PC; Schünemann MH; Kohlschütter A; Hoffman GF
    J Pediatr; 1990 Apr; 116(4):665-6. PubMed ID: 2319411
    [No Abstract]   [Full Text] [Related]  

  • 8. Phenylalanine metabolites as indicators of dietary compliance in children with phenylketonuria.
    Michals K; Lopus M; Matalon R
    Biochem Med Metab Biol; 1988 Feb; 39(1):18-23. PubMed ID: 3355711
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Significant phenylalanine hydroxylation in vivo in patients with classical phenylketonuria.
    Thompson GN; Halliday D
    J Clin Invest; 1990 Jul; 86(1):317-22. PubMed ID: 2365821
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenylalanine metabolism in the phenylpyruvic condition. I. Distribution, pool size, and turnover rate in human phenylketonuria.
    GRUMER HD; KOBLET H; WOODARD C
    J Clin Invest; 1961 Sep; 40(9):1758-65. PubMed ID: 13709234
    [No Abstract]   [Full Text] [Related]  

  • 11. Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
    ARMSTRONG MD; TYLER FH
    J Clin Invest; 1955 Apr; 34(4):565-80. PubMed ID: 14367510
    [No Abstract]   [Full Text] [Related]  

  • 12. [Phenylalanine metabolism disorders in phenylketonuria (review)].
    D'iachkova AIa; Lebedev BV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1969; 69(10):1588-91. PubMed ID: 4905361
    [No Abstract]   [Full Text] [Related]  

  • 13. The need of essential amino acids in children. An evaluation based on the intake of phenylalanine, tyrosine, leucine, isoleucine, and valine in children with phenylketonuria, tyrosine amino transferase defect, and maple syrup urine disease.
    Kindt E; Halvorsen S
    Am J Clin Nutr; 1980 Feb; 33(2):279-86. PubMed ID: 6101930
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effects of folic and folinic acids on the metabolism of phenylalanine in phenylketonuria.
    Copenhaver JH; Carver MJ; Schain RJ
    Metabolism; 1965 Dec; 14(12):1233-6. PubMed ID: 5294700
    [No Abstract]   [Full Text] [Related]  

  • 15. In vivo disposal of phenylalanine in phenylketonuria: a study of two siblings.
    Treacy E; Pitt JJ; Seller K; Thompson GN; Ramus S; Cotton RG
    J Inherit Metab Dis; 1996; 19(5):595-602. PubMed ID: 8892014
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Decreased essential amino acid requirements without catabolism in phenylketonuria and maple syrup urine disease.
    Ruch T; Kerr D
    Am J Clin Nutr; 1982 Feb; 35(2):217-28. PubMed ID: 7064884
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenylalanine and tyrosine metabolism in phenylketonuria heterozygotes: influence of different phenylalanine hydroxylase mutations.
    Spada M; Dianzani I; Bonetti G; Biondi A; Leone L; Giannattasio S; Ponzone A
    J Inherit Metab Dis; 1998 Jun; 21(3):236-9. PubMed ID: 9686365
    [No Abstract]   [Full Text] [Related]  

  • 18. Use of handheld computers for assessment of prefrontal cortex function in patients with phenylketonuria.
    Bik-Multanowski M; Mozrzymas R; Nowacka M; Borawska-Kowalczyk U; Lange A; Starostecka E; Didycz B; Kaluzny L; Gizewska M; Szynaka E; Szymczakiewicz-Multanowska A;
    Mol Genet Metab; 2005 Dec; 86 Suppl 1():S142-4. PubMed ID: 16165388
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Individual blood-brain barrier phenylalanine transport in siblings with classical phenylketonuria.
    Weglage J; Wiedermann D; Denecke J; Feldmann R; Koch HG; Ullrich K; Möller HE
    J Inherit Metab Dis; 2002 Oct; 25(6):431-6. PubMed ID: 12555936
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Minimally invasive (13)C-breath test to examine phenylalanine metabolism in children with phenylketonuria.
    Turki A; Murthy G; Ueda K; Cheng B; Giezen A; Stockler-Ipsiroglu S; Elango R
    Mol Genet Metab; 2015; 115(2-3):78-83. PubMed ID: 25943030
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.