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.
138 related articles for article (PubMed ID: 17701224)
21. Efficacy and safety of allopurinol in patients with the Lesch-Nyhan syndrome and partial hypoxanthine- phosphoribosyltransferase deficiency: a follow-up study of 18 Spanish patients. Torres RJ; Prior C; Puig JG Nucleosides Nucleotides Nucleic Acids; 2006; 25(9-11):1077-82. PubMed ID: 17065067 [TBL] [Abstract][Full Text] [Related]
22. Hyperuricaemia associated with 18q deletion. Atypical Lesch-Nyhan syndrome? Laszlo A; Osztovics M; Dallmann L; Mattyus A Ann Genet; 1981; 24(1):17-20. PubMed ID: 6971610 [TBL] [Abstract][Full Text] [Related]
23. HPRT deficiency in a two-month-old child presenting acute renal failure and gout with a new deletion of two bases in exon 3 of the HPRT gene. Zamora A; Escárcega RO; Vazquez R; Zamora A; O'Neill JP Arch Med Res; 2007 May; 38(4):460-2. PubMed ID: 17416296 [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]
29. Genetic analysis of the HPRT mutation of Lesch-Nyhan syndrome in a Chinese family. Lee WJ; Lee HM; Chi CS; Yang MT; Lin HY; Lin WH Zhonghua Yi Xue Za Zhi (Taipei); 1995 Dec; 56(6):359-66. PubMed ID: 8851475 [TBL] [Abstract][Full Text] [Related]
30. Acute renal failure in an infant with partial deficiency of hypoxanthine-guanine phosphoribosyltransferase. Wingen AM; Löffler W; Waldherr R; Schärer K Proc Eur Dial Transplant Assoc Eur Ren Assoc; 1985; 21():751-5. PubMed ID: 3991573 [TBL] [Abstract][Full Text] [Related]
32. Recurrent kidney stones in a child with Lesch-Nyhan syndrome: Answers. Ng N; Kaur A; Shenoy M Pediatr Nephrol; 2019 Mar; 34(3):425-427. PubMed ID: 30112657 [No Abstract] [Full Text] [Related]
33. Eighteen-year follow-up of a patient with partial hypoxanthine phosphoribosyltransferase deficiency and a new mutation. Gregoric A; Rabelink GM; Kokalj Vokac N; Varda NM; Zagradisnik B Pediatr Nephrol; 2005 Sep; 20(9):1346-8. PubMed ID: 15965771 [TBL] [Abstract][Full Text] [Related]
34. Atlantoaxial subluxation with recurrent consciousness disturbance in a boy with Lesch-Nyhan syndrome. Hou JW Acta Paediatr; 2006 Nov; 95(11):1500-4. PubMed ID: 17062485 [TBL] [Abstract][Full Text] [Related]
35. [Xanthine lithiasis in a case of Lesch-Nyhan syndrome treated with allopurinol]. Loris Pablo C; Oliván del Cacho MJ; Heras Gironella M; Sierra Sirvant J; Martínez Escribano MP; Izaguirre Zugazaga C; Lázaro Castillo J; March A An Esp Pediatr; 1983 Nov; 19(5):401-4. PubMed ID: 6660658 [TBL] [Abstract][Full Text] [Related]
36. Urate nephropathy associated with impaired kinetic properties of hypoxanthine phosphoribosyl transferase in a 45-day-old infant. Singal R; Krishnamurthy S; Narayanan P; Rajesh NG; Choudhary B; Jacomelli G; Micheli V Clin Exp Nephrol; 2012 Feb; 16(1):164-7. PubMed ID: 21904906 [TBL] [Abstract][Full Text] [Related]
37. The Lesch-Nyhan syndrome: a family study. Pullon DH; Ballantyne GH; Webster D; Becroft DM N Z Med J; 1977 Dec; 86(601):518-21. PubMed ID: 272569 [TBL] [Abstract][Full Text] [Related]
38. Renal sonography in long standing Lesch-Nyhan syndrome. Kenney IJ Clin Radiol; 1991 Jan; 43(1):39-41. PubMed ID: 1999070 [TBL] [Abstract][Full Text] [Related]