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 *

149 related articles for article (PubMed ID: 460359)

  • 1. Diagnosis and management of "malignant hyperphenylalaninemia".
    Cederbaum SD
    N Engl J Med; 1979 Aug; 301(8):441-2. PubMed ID: 460359
    [No Abstract]   [Full Text] [Related]  

  • 2. [Interpretation of the consensus about the diagnosis and treatment of hyperphenylalaninemia].
    Ye J; Gu X
    Zhonghua Er Ke Za Zhi; 2014 Jun; 52(6):430-2. PubMed ID: 25190162
    [No Abstract]   [Full Text] [Related]  

  • 3. [Consensus about the diagnosis and treatment of hyperphenylalaninemia].
    Yang Y; Ye Y; ; ; ;
    Zhonghua Er Ke Za Zhi; 2014 Jun; 52(6):420-5. PubMed ID: 25190160
    [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. Evaluation of neonatal BH4 loading test in neonates screened for hyperphenylalaninemia.
    Feillet F; Chery C; Namour F; Kimmoun A; Favre E; Lorentz E; Battaglia-Hsu SF; Guéant JL
    Early Hum Dev; 2008 Sep; 84(9):561-7. PubMed ID: 18321666
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The metabolic and molecular bases of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.
    Blau N; Erlandsen H
    Mol Genet Metab; 2004 Jun; 82(2):101-11. PubMed ID: 15171997
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Tetrahydrobiopterin loading test in differential diagnosis among hyperphenylalaninemia patients].
    Zhang ZX; Ye J; Qiu WJ; Han LS; Gu XF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):438-40. PubMed ID: 16086286
    [TBL] [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. Review of current practices in management of inherited disorders of amino acid metabolism in Western Europe.
    Wachtel U
    Hum Nutr Appl Nutr; 1986; 40 Suppl 1():61-9. PubMed ID: 3528074
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Hyperphenylalaninemia in 1981. A diagnostic approach (author's transl)].
    Dhondt JL; Farriaux JP
    Arch Fr Pediatr; 1981 Oct; 38(8):573-8. PubMed ID: 7316669
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenylketonuria variants.
    Niederwieser A; Curtius HC; Viscontini M; Schaub J; Schmidt H
    Lancet; 1979 Mar; 1(8115):550. PubMed ID: 85126
    [No Abstract]   [Full Text] [Related]  

  • 12. [Hyperphenylalaninemia in 1983].
    Farriaux JP; Dhont JL
    Rev Med Brux; 1983 Apr; 4(4):305-10. PubMed ID: 6878937
    [No Abstract]   [Full Text] [Related]  

  • 13. Unsolved problems in diagnosis and therapy of hyperphenylalaninemia caused by defects in tetrahydrobiopterin metabolism.
    Kaufman S
    J Pediatr; 1986 Oct; 109(4):572-8. PubMed ID: 3489828
    [No Abstract]   [Full Text] [Related]  

  • 14. [Hyperphenylalaninaemia with normal phenylalanine-hydroxylase activity and a deficiency of tetrahydrobiopterin and dihydropteridine reductase].
    Rey F; Harpey JP; Leeming RJ; Blair JA; Aicardi J; Rey J
    Arch Fr Pediatr; 1977; 34(7 Suppl):CIX-CXX. PubMed ID: 931522
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Atypical form of phenylketonuria caused by lack of dihydrobiopterin synthetase activity].
    Słowik M; Mańkowski T
    Pol Tyg Lek; 1992 Mar 2-9; 47(9-10):236-7. PubMed ID: 1437828
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Differential diagnosis and therapy of various forms of hyperphenylalaninemia: facts and fiction].
    Endres W
    Wien Klin Wochenschr; 1992; 104(16):503-9. PubMed ID: 1413808
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Plasma biopterin levels and tetrahydrobiopterin responsiveness.
    Shintaku H; Fujioka H; Sawada Y; Asada M; Yamano T
    Mol Genet Metab; 2005 Dec; 86 Suppl 1():S104-6. PubMed ID: 16183315
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hyperphenylalaninemia due to a deficiency of biopterin. A variant form of phenylketonuria.
    Kaufman S; Berlow S; Summer GK; Milstien S; Schulman JD; Orloff S; Spielberg S; Pueschel S
    N Engl J Med; 1978 Sep; 299(13):673-9. PubMed ID: 683251
    [TBL] [Abstract][Full Text] [Related]  

  • 19. American Academy of Pediatrics. Committee on Nutrition. New developments in hyperphenylalaninemia.
    Pediatrics; 1980 Apr; 65(4):844-6. PubMed ID: 7367099
    [No Abstract]   [Full Text] [Related]  

  • 20. [Determination of phenylalanine-4-hydroxylase as a parameter in the differential diagnosis of hyperphenylalaninemia].
    Kukla L; Mrskos A; Pijácková A; Podhradská O
    Cesk Pediatr; 1987 Sep; 42(9):542-5. PubMed ID: 3664770
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.