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 *

148 related articles for article (PubMed ID: 8156315)

  • 21. Acute renal failure due to bilateral xanthine urolithiasis in a boy with Lesch-Nyhan syndrome.
    Sikora P; Pijanowska M; Majewski M; Bieniaś B; Borzecka H; Zajczkowska M
    Pediatr Nephrol; 2006 Jul; 21(7):1045-7. PubMed ID: 16773422
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Clinical spectrum of hypoxanthine-guanine phosphoribosyltransferase deficiency: study of 12 cases].
    García Puig J; Mateos FA; Jiménez ML; Arcas J; Miranda ME; Oríz Vázquez J
    Med Clin (Barc); 1994 May; 102(18):681-7. PubMed ID: 8028417
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Late diagnosis of Lesch-Nyhan disease variant.
    Doucet BP; Jegatheesan D; Burke J
    BMJ Case Rep; 2013 Dec; 2013():. PubMed ID: 24326440
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Acute renal failure during adenine therapy in Lesch-Nyhan syndrome.
    Ceccarelli M; Ciompi ML; Pasero G
    Adv Exp Med Biol; 1974; 41():671-5. PubMed ID: 4832594
    [No Abstract]   [Full Text] [Related]  

  • 25. Kelley-Seegmiller syndrome in a patient with complete hypoxanthine-guanine phosphoribosyltransferase deficiency.
    Cossu A; Micheli V; Jacomelli G; Carcassi A
    Clin Exp Rheumatol; 2002; 20(6):851-3. PubMed ID: 12508781
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Acute renal failure unmasking Lesch-Nyhan disease in a patient with tuberous sclerosis complex.
    Thumfart J; Weschke B; Ringe H; Weinhold N; Müller D
    Eur J Paediatr Neurol; 2016 Jul; 20(4):649-51. PubMed ID: 27185581
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [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]  

  • 28. Clinical correlations in partial hypoxanthine guanine phosphoribosyltransferase deficiency.
    Hersh JH; Page T; Hand ME; Seegmiller JE; Nyhan WL; Weisskopf B
    Pediatr Neurol; 1986; 2(5):302-4. PubMed ID: 3508703
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Renal oxypurine deposition in Lesch-Nyhan syndrome: sonographic evaluation.
    Stevens SK; Parker BR
    Pediatr Radiol; 1989; 19(6-7):479-80. PubMed ID: 2671903
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Impaired kinetic properties of hypoxanthine-guanine phosphoribosyl transferase as a cause of uric acid nephropathy in early infancy.
    Kerem E; Branski D; Gross-Kieselstein E; Hurvitz H; Abrahamov A; Pollack Y
    Eur J Pediatr; 1987 Nov; 146(6):595-7. PubMed ID: 3428293
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hypoxanthine-guanine phosphoribosyl transferase (HGPRT) deficiency in a girl.
    Ogasawara N; Kashiwamata S; Oishi H; Hara K; Watanabe K; Miyazaki S; Kumagai T; Hakamada S
    Adv Exp Med Biol; 1984; 165 Pt A():13-8. PubMed ID: 6720366
    [No Abstract]   [Full Text] [Related]  

  • 32. Lesch-Nyhan Syndrome: report on two brothers.
    Yang MT; Mak SC; Chi CS; Lin HY; Lii YP; Wu KH; Shian WJ
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994; 35(6):552-8. PubMed ID: 7831990
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Differential diagnosis of cerebral palsy: Lesch-Nyhan syndrome without self-mutilation.
    Mitchell G; McInnes RR
    Can Med Assoc J; 1984 May; 130(10):1323-4. PubMed ID: 6722697
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Nephrocalcinosis and Renal Failure in Lesch-Nyhan Syndrome: Report of Two Familial Cases and Review of the Literature.
    Vargiami E; Printza N; Papadimiditriou E; Batzios S; Kyriazi M; Papachristou F; Zafeiriou DI
    Urology; 2016 Nov; 97():194-196. PubMed ID: 27079129
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Determination of Activity of the Enzymes Hypoxanthine Phosphoribosyl Transferase (HPRT) and Adenine Phosphoribosyl Transferase (APRT) in Blood Spots on Filter Paper.
    Auler K; Broock R; Nyhan WL
    Curr Protoc Hum Genet; 2015 Jul; 86():17.19.1-17.19.10. PubMed ID: 26132002
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Purine metabolism in heterozygous carriers of hypoxanthine-guanine phosphoribosyltransferase deficiency.
    Emmerson BT; Wyngaarden JB
    Science; 1969 Dec; 166(3912):1533-5. PubMed ID: 17695080
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [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]  

  • 38. Lesch-Nyhan syndrome: the synthesis of inosine 5'-phosphate in the hypoxanthine-guanine phosphoribosyltransferase-deficient erythrocyte by alternate biochemical pathways.
    Lowy BA; Williams MK
    Pediatr Res; 1977 May; 11(5):691-4. PubMed ID: 870876
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Evaluation of the severity of hypoxanthine-guanine phosphoribosyltransferase deficiency using viable T cells.
    Yamanaka H; Kamatani N; Nishoka K; Kobayashi M; Wada Y; Ohtani T; Mikanagi K
    Hum Hered; 1985; 35(6):358-63. PubMed ID: 3876977
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Lesch-Nyhan syndrome: evidence for abnormal adrenergic function.
    Rockson S; Stone R; Van der Weyden M; Kelley WN
    Science; 1974 Dec; 186(4167):934-5. PubMed ID: 4469689
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.