BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

318 related articles for article (PubMed ID: 7432385)

  • 1. Phenylketonuria: epitome of human biochemical genetics (second of two parts).
    Scriver CR; Clow CL
    N Engl J Med; 1980 Dec; 303(24):1394-400. PubMed ID: 7432385
    [No Abstract]   [Full Text] [Related]  

  • 2. Phenylketonuria: epitome of human biochemical genetics (first of two parts).
    Scriver CR; Clow CL
    N Engl J Med; 1980 Dec; 303(23):1336-42. PubMed ID: 7001231
    [No Abstract]   [Full Text] [Related]  

  • 3. Treated phenylketonuria: intelligence and blood phenylalanine levels.
    Fuller R; Shuman J
    Am J Ment Defic; 1971 Mar; 75(5):539-45. PubMed ID: 5551499
    [No Abstract]   [Full Text] [Related]  

  • 4. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.
    Güttler F
    Acta Paediatr Scand Suppl; 1980; 280():1-80. PubMed ID: 7006308
    [No Abstract]   [Full Text] [Related]  

  • 5. Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuria.
    Hennermann JB; Loui A; Weber A; Mönch E
    J Perinat Med; 2004; 32(4):383-5. PubMed ID: 15346830
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Our experiences with treatment of phenylketonuria].
    Tresohlavá Z; Brachfeld K; Svatý J
    Cesk Pediatr; 1969 Jun; 24(6):522-8. PubMed ID: 5792287
    [No Abstract]   [Full Text] [Related]  

  • 7. Phenylketonuria and its variants.
    Kaufman S
    Adv Hum Genet; 1983; 13():217-97. PubMed ID: 6362361
    [No Abstract]   [Full Text] [Related]  

  • 8. Neonatal hyperphenylalaninemia: a differential diagnosis.
    Menkes JH; Holtzman NA
    Neuropadiatrie; 1970 Apr; 1(4):434-46. PubMed ID: 5538081
    [No Abstract]   [Full Text] [Related]  

  • 9. Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia.
    Cunningham GC; Day RW; Berman JL; Hsia DY
    Am J Dis Child; 1969 Jun; 117(6):626-35. PubMed ID: 5771502
    [No Abstract]   [Full Text] [Related]  

  • 10. Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria.
    Ponzone A; Spada M; Roasio L; Porta F; Mussa A; Ferraris S
    J Pediatr Gastroenterol Nutr; 2008 May; 46(5):561-9. PubMed ID: 18493213
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The problem of maternal phenylketonuria.
    MacCready RA; Levy HL
    Am J Obstet Gynecol; 1972 May; 113(1):121-8. PubMed ID: 5024993
    [No Abstract]   [Full Text] [Related]  

  • 12. Phenylketonemia in phenylketonuria.
    Partington MW; Vickery SK
    Neuropadiatrie; 1974 May; 5(2):125-37. PubMed ID: 4407755
    [No Abstract]   [Full Text] [Related]  

  • 13. Phenylketonuria: intellectual developmental and early treatment.
    O'Grady DJ; Berry HK; Sutherland BS
    Dev Med Child Neurol; 1970 Jun; 12(3):343-7. PubMed ID: 5433150
    [No Abstract]   [Full Text] [Related]  

  • 14. The correlation of genotype and phenotype in Portuguese hyperphenylalaninemic patients.
    Rivera I; Cabral A; Almeida M; Leandro P; Carmona C; Eusébio F; Tasso T; Vilarinho L; Martins E; Lechner MC; de Almeida IT; Konecki DS; Lichter-Konecki U
    Mol Genet Metab; 2000 Mar; 69(3):195-203. PubMed ID: 10767174
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new variant form of phenylketonuria.
    Watts RW; Purkiss P; Chalmers RA
    Q J Med; 1979 Jul; 48(191):403-17. PubMed ID: 317358
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disorders.
    Ledley FD; Levy HL; Woo SL
    N Engl J Med; 1986 May; 314(20):1276-80. PubMed ID: 3702929
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Newborn screening for phenylketonuria: thirty years of progress.
    O'Flynn ME
    Curr Probl Pediatr; 1992 Apr; 22(4):159-65. PubMed ID: 1576829
    [No Abstract]   [Full Text] [Related]  

  • 18. Prenatal diagnosis of classical phenylketonuria by gene mapping.
    Woo SL; Lidsky AS; Güttler F; Thirumalachary C; Robson KJ
    JAMA; 1984 Apr; 251(15):1998-2002. PubMed ID: 6700105
    [No Abstract]   [Full Text] [Related]  

  • 19. [Congenital errors of metabolism: phenylketonuria and hyperphenylalanemias].
    Laguna Serrano C
    An R Acad Nac Med (Madr); 1982; 99(4):783-814. PubMed ID: 7185286
    [No Abstract]   [Full Text] [Related]  

  • 20. [Current problems in the diagnosis and treatment of phenylketonuria].
    Sanielevici-Marinov S; Anagnoste V; Mark E; Tomescu E; Iordache C
    Pediatria (Bucur); 1973; 22(1):1-12. PubMed ID: 4733556
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 16.