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6. 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]
7. 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]
8. [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]
9. Letter: Pterin administration as a therapy for P.K.U. due to dihydropteridine-reductase deficiency? Kaufman S Lancet; 1975 Oct; 2(7938):767. PubMed ID: 52788 [No Abstract] [Full Text] [Related]
10. A mild case of dihydropteridine reductase deficiency with residual activity in erythrocytes. Nakabayashi H; Owada M; Kitagawa T J Inherit Metab Dis; 1984; 7(3):135-6. PubMed ID: 6438398 [No Abstract] [Full Text] [Related]
11. [Follow up protocol of patients with hyperphenylalaninemia]. Alvarez Domínguez L; Riverola de Veciana AT; Campistol Plana J; Castillo Rivera P; Maya Victoria A; Prats Coll R An Esp Pediatr; 1990 Nov; 33(5):457-9. PubMed ID: 2096760 [TBL] [Abstract][Full Text] [Related]
12. [Clinical diagnosis of hyperphenylalaninemia in the newborn infant and infant stages]. Simková M; Hyánek J; Karger P; Hoza J; Holub J; Viletová H Cesk Pediatr; 1976 Nov; 31(11):619-21. PubMed ID: 1035139 [No Abstract] [Full Text] [Related]
14. 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]
15. [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]
16. [Measurement in samples of dry blood of dihydropteridine reductase and ratio of total biopterin in hyperphenylalaninemia and other neurological diseases]. Leeming RJ; Karim AR; Sahota AS; Blair JA; Green A Arch Fr Pediatr; 1987; 44 Suppl 1():649-54. PubMed ID: 3449009 [No Abstract] [Full Text] [Related]
17. 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]
18. Progressive intracranial calcification in dihydropteridine reductase deficiency prior to folinic acid therapy. Woody RC; Brewster MA; Glasier C Neurology; 1989 May; 39(5):673-5. PubMed ID: 2785251 [TBL] [Abstract][Full Text] [Related]
19. Tetrahydrofolate and hydroxocobolamin in the management of dihydropteridine reductase deficiency. Leeming RJ; Harpey JP; Brown SM; Blair JA J Ment Defic Res; 1982 Mar; 26(Pt 1):21-5. PubMed ID: 6978943 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]