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.
135 related articles for article (PubMed ID: 656085)
1. Adenine phosphoribosyl transferase deficiency in association with sub-normal hypoxanthine phophoribosyl transferase in families of Lesch--Nyhan patients. Itiaba K; Melançon SB; Dallaire L; Crawhall JC Biochem Med; 1978 Apr; 19(2):252-9. PubMed ID: 656085 [No Abstract] [Full Text] [Related]
2. Prenatal diagnosis of Lesch-Nyhan syndrome and some characteristics of hypoxanthine-guanine phosphoribosyltransferase and adenine phosphoribosyltransferase in human tissues and cultivated cells. Shin-Buehring YS; Osang M; Wirtz A; Haas B; Rahm P; Schaub J Pediatr Res; 1980 Jun; 14(6):825-9. PubMed ID: 7402756 [TBL] [Abstract][Full Text] [Related]
4. Simple screening methods for hypoxanthine-guanine phosphoribosyltransferase and adenine phosphoribosyltransferase deficiencies using dried blood spots on filter paper. Nishida Y; Miyamoto T Ann Clin Biochem; 1986 Sep; 23 ( Pt 5)():529-32. PubMed ID: 3767288 [TBL] [Abstract][Full Text] [Related]
5. [A new form of the Lesch-Nyhan syndrome. A study of hypoxanthine-guanine-phosphoribosyl-transferase in fibroblasts. The in vitro and in vivo effect of adenine on enzyme activity]. Warter S; Bieth R Ann Biol Clin (Paris); 1982; 40(5):561-6. PubMed ID: 6186166 [TBL] [Abstract][Full Text] [Related]
6. A female case of the Leach-Nyhan syndrome. Hara K; Kashiwamata S; Ogasawara N; Ohishi H; Natsume R; Yamanaka T; Hakamada S; Miyazaki S; Watanabe K Tohoku J Exp Med; 1982 Jul; 137(3):275-82. PubMed ID: 7112549 [TBL] [Abstract][Full Text] [Related]
7. Simple screening methods for disorders of purine metabolism using dried blood and or urine spots on filter paper. Nishida Y; Takeuchi F; Miyamoto T Adv Exp Med Biol; 1989; 253A():123-7. PubMed ID: 2624180 [No Abstract] [Full Text] [Related]
8. Partial hypoxanthine-guanine phosphoribosyl transferase deficiency with full expression of the Lesch-Nyhan syndrome. Rijksen G; Staal GE; van der Vlist MJ; Beemer Fa; Troost J; Gutensohn W; van Laarhoven JP; de Bruyn CH Hum Genet; 1981; 57(1):39-47. PubMed ID: 7262868 [No Abstract] [Full Text] [Related]
9. [Activity of erythrocyte purine phosphoribosyltransferases in Lesch-Nyhan syndrome]. Aleksandrova LA; Shaposhnikov AM Vopr Med Khim; 1981; 27(2):215-20. PubMed ID: 7281560 [TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis by enzyme analysis in 15 pregnancies at risk for the Lesch-Nyhan syndrome. Graham GW; Aitken DA; Connor JM Prenat Diagn; 1996 Jul; 16(7):647-51. PubMed ID: 8843475 [TBL] [Abstract][Full Text] [Related]
12. High-performance liquid chromatographic method for simultaneous screening of the deficiencies of APRT and HPRT. Nishina T; Sakuma R; Kojima T; Kiyamura M; Kamatani N; Nishioka K Adv Exp Med Biol; 1989; 253A():59-65. PubMed ID: 2483031 [No Abstract] [Full Text] [Related]
13. Quantitative radiochemical enzyme assays in single cells: purine phosphoribosyl transferase activities in cultured fibroblasts. de Bruyn CH; Oei TL; Hösli P Biochem Biophys Res Commun; 1976 Jan; 68(2):483-8. PubMed ID: 1252240 [No Abstract] [Full Text] [Related]
14. Genetic heterogeneity of hypoxanthine-phosphoribosyl transferase in human fibroblasts of 3 families. Willers I; Held KR; Singh S; Goedde HW Clin Genet; 1977 Mar; 11(3):193-200. PubMed ID: 837570 [TBL] [Abstract][Full Text] [Related]
15. Production of a model for Lesch-Nyhan syndrome in hypoxanthine phosphoribosyltransferase-deficient mice. Wu CL; Melton DW Nat Genet; 1993 Mar; 3(3):235-40. PubMed ID: 8485579 [TBL] [Abstract][Full Text] [Related]
16. [Lesch-Nyhan syndrome: a new variant with hypoxanthine-guanine phosphoriboxyl transferase activity higher than the classical disease and detection of the heterozygote trait in the erythrocytes of the carrier]. Hernández Nieto L; Nyhan WL; Page T; Cubillo Ferreira G; Rodríguez Fernández M; González García T; Cabrera de León A; Santolaria Fernández FJ Med Clin (Barc); 1985 Jan; 84(2):68-71. PubMed ID: 3974350 [No Abstract] [Full Text] [Related]
17. [Erythrocyte purine phosphoribosyltransferase activity in girls with the Lesch-Nyhan syndrome]. Aleksandrova LA; Shaposhnikov AM Vopr Med Khim; 1981; 27(4):488-92. PubMed ID: 7293080 [TBL] [Abstract][Full Text] [Related]
18. Problems in diagnosis and treatment of adenine and hypoxanthine-guanine phosphoribosyltransferase deficiency. Dillon MJ; Simmonds HA; Barratt TM; Fairbanks LD; Holland PC Adv Exp Med Biol; 1984; 165 Pt A():1-6. PubMed ID: 6720360 [No Abstract] [Full Text] [Related]
19. Lesch-Nyhan syndrome: biochemical characterization of a case with attenuated behavioral manifestation. Fattal A; Spirer Z; Zoref-Shani E; Sperling O Enzyme; 1984; 31(1):55-60. PubMed ID: 6201351 [TBL] [Abstract][Full Text] [Related]
20. [Effect of a purine-free diet on the purine phosphoribosyltransferase activity of erythrocytes in patients with Lesch-Nyhan syndrome]. Semenova IA; Pen'kovskaia NP Vopr Med Khim; 1984; 30(4):94-7. PubMed ID: 6506590 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]