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 *

93 related articles for article (PubMed ID: 4049790)

  • 1. [Active form of dihydropteridine reductase in human chorion cells. Possibility of prenatal diagnosis].
    Gromov PS; Bakharev VA; Annenkov GA
    Vopr Med Khim; 1985; 31(4):73-5. PubMed ID: 4049790
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Diagnosis of dihydropteridine reductase deficiency by erythrocyte enzyme assay.
    Narisawa K; Arai N; Hayakawa H; Tada K
    Pediatrics; 1981 Oct; 68(4):591-2. PubMed ID: 7322696
    [No Abstract]   [Full Text] [Related]  

  • 3. Hyperphenylalaninemia due to dihydropteridine reductase deficiency: diagnosis by measurement of oxidized and reduced pterins in urine.
    Milstien S; Kaufman S; Summer GK
    Pediatrics; 1980 Apr; 65(4):806-10. PubMed ID: 7367090
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hyperphenylalaninemia due to dihydropteridine reductase deficiency: diagnosis by enzyme assays on dried blood spots.
    Arai N; Narisawa K; Hayakawa H; Tada K
    Pediatrics; 1982 Sep; 70(3):426-30. PubMed ID: 7110817
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Malignant hyperphenylalaninemia with dihydropteridine reductase deficiency].
    Hyánek J; Zeman J; Niederwieser A; Leeming R; Grimm U; Sahota A; Komárek V; Houst'ková H; Böhm J; Verner P
    Cesk Pediatr; 1986 Nov; 41(11):664-8. PubMed ID: 3791474
    [No Abstract]   [Full Text] [Related]  

  • 6. [Dihydropteridine reductase activity in leukocytes and cultured fibroblasts of health individuals and of patients with the classical form of phenylketonuria].
    Gromov PS; Val'iano NM; Akhunov VS; Annenkov GA
    Vopr Med Khim; 1983; 29(5):66-9. PubMed ID: 6649535
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The use of restriction fragment length polymorphisms in prenatal diagnosis of dihydropteridine reductase deficiency.
    Dahl HH; Wake S; Cotton RG; Danks DM
    J Med Genet; 1988 Jan; 25(1):25-8. PubMed ID: 2895188
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic fluid cells.
    Milstien S; Holtzman NA; O'Flynn ME; Thomas GH; Butler IJ; Kaufman S
    J Pediatr; 1976 Nov; 89(5):763-6. PubMed ID: 978323
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dihydropteridine reductase deficiency diagnosis by assays on peripheral blood-cells.
    Firgaira FA; Cotton RG; Danks DM
    Lancet; 1979 Dec; 2(8155):1260-3. PubMed ID: 93181
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dihydropteridine reductase deficiency diagnosis by assays on peripheral blood cells.
    Firgaira FA; Cotton RG; Danks DM
    Lancet; 1980 Jan; 1(8160):160. PubMed ID: 6101503
    [No Abstract]   [Full Text] [Related]  

  • 11. Prenatal determination of dihydropteridine reductase in a normal fetus at risk for malignant hyperphenylalaninemia.
    Firgaira FA; Cotton RG; Danks DM; Fowler K; Lipson A; Yu JS
    Prenat Diagn; 1983 Jan; 3(1):7-11. PubMed ID: 6844267
    [No Abstract]   [Full Text] [Related]  

  • 12. Dihydropteridine reductase deficiency: diagnosis by leukocyte enzyme assay.
    Narisawa K; Arai N; Ishizawa S; Ogasawara Y; Onuma A; Iinuma K; Tada K
    Clin Chim Acta; 1980 Aug; 105(3):335-42. PubMed ID: 7408193
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Urinary dihydroxanthopterin in the diagnosis of malignant hyperphenylalaninemia and phenylketonuria.
    Schlesinger P; Watson BM; Cotton RG; Danks DM
    Clin Chim Acta; 1979 Mar; 92(2):187-95. PubMed ID: 487572
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenylketonuria due to dihydropteridine reductase deficiency: presentation of two cases.
    Longhi R; Riva E; Valsasina R; Paccanelli S; Giovannini M
    J Inherit Metab Dis; 1985; 8 Suppl 2():97-8. PubMed ID: 3930875
    [No Abstract]   [Full Text] [Related]  

  • 15. Atypical phenylketonuria with normal dihydropteridine reductase activity.
    Rey F; Blandin-Savoja F; Rey J
    N Engl J Med; 1976 Nov; 295(20):1138-9. PubMed ID: 980015
    [No Abstract]   [Full Text] [Related]  

  • 16. Hyperphenylalaninemia caused by dihydropteridine reductase deficiency in children receiving chemotherapy for acute lymphoblastic leukemia.
    Blau N; Curtius AC; Kierat L; Leupold D; Kohne E
    J Pediatr; 1989 Oct; 115(4):661-3. PubMed ID: 2795366
    [No Abstract]   [Full Text] [Related]  

  • 17. Brain CT and MR findings in hyperphenylalaninemia due to dihydropteridine reductase deficiency (variant of phenylketonuria).
    Sugita R; Takahashi S; Ishii K; Matsumoto K; Ishibashi T; Sakamoto K; Narisawa K
    J Comput Assist Tomogr; 1990; 14(5):699-703. PubMed ID: 2398144
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neonatal screening for dihydropteridine reductase deficiency.
    Sahota A; Blair JA; Barford PA; Leeming RJ; Green A; Pollitt RJ
    J Inherit Metab Dis; 1985; 8 Suppl 2():99-100. PubMed ID: 3930876
    [No Abstract]   [Full Text] [Related]  

  • 19. Basal ganglion calcification in hyperphenylalaninemia due to deficiency of dihydropteridine reductase.
    Schmidt H; Ullrich K; Korinthenberg R; Peters PE
    Pediatr Radiol; 1988; 19(1):54-6. PubMed ID: 3222065
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Heterogeneity of the molecular defect in human dihydropteridine reductase deficiency.
    Firgaira FA; Choo KH; Cotton RG; Danks DM
    Biochem J; 1981 Sep; 198(3):677-82. PubMed ID: 7326033
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.