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24. [Cerebral blood flow perfusion imaging by single photon emission computed tomography in patients with early syphilis]. Shi X; Wu J; Liu Z; Tang J; Su Y Zhonghua Yi Xue Za Zhi; 2002 May; 82(9):580-2. PubMed ID: 12133474 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. [Xanthinuria with xanthine lithiasis in a patient with Lesch-Nyhan syndrome under allopurinol therapy]. Rebentisch G; Stolz S; Muche J Aktuelle Urol; 2004 Jun; 35(3):215-21. PubMed ID: 15258855 [TBL] [Abstract][Full Text] [Related]
27. Normal B-lymphocyte function in patients with Lesch-Nyhan syndrome and HGPRT deficiency. Gelfand EW; Fox IH; Stuckey M; Dosch HM Clin Exp Immunol; 1978 Feb; 31(2):205-8. PubMed ID: 306325 [TBL] [Abstract][Full Text] [Related]
28. Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3). Gustavsson P; Kimber E; Wahlström J; Annerén G Am J Med Genet; 1999 Feb; 82(4):348-51. PubMed ID: 10051171 [TBL] [Abstract][Full Text] [Related]
29. An error in the code: what can a rare disorder tell us about human behavior? Preston R New Yorker; 2007 Aug; ():30-6. PubMed ID: 17715509 [No Abstract] [Full Text] [Related]
30. [Report of a patient with Lesch-Nyhan syndrome caused by total deficiency of HGPRT and with normal activity in female family members]. Ferrández A; Mayayo E; Nyhan WL; Bakay B An Esp Pediatr; 1982 Jul; 17(1):60-4. PubMed ID: 7137725 [TBL] [Abstract][Full Text] [Related]
31. [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]
32. [The Lesch-Nyhan syndrome]. Peco-Antić A; Smoljanić Z; Dimitrijević N; Kostić M; Marsenić O; Djordjević M; Kruscić D Srp Arh Celok Lek; 2001; 129(9-10):260-3. PubMed ID: 11928606 [TBL] [Abstract][Full Text] [Related]
34. [Encephalopathy with self mutilations in a twin. Normal HGPRT activity. Hyperuricosuria without major hyperuricemia. Apropos of the limits of the Lesch-Nyham syndrome]. Champanier JP; Etienne JC; Gougeon J; Pascalis G Rev Neuropsychiatr Infant; 1972 Oct; 20(10):777-84. PubMed ID: 4650284 [No Abstract] [Full Text] [Related]
35. 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]
36. Lesch-Nyhan syndrome: a study of motor behavior and cerebrospinal fluid neurotransmitters. Jankovic J; Caskey TC; Stout JT; Butler IJ Ann Neurol; 1988 May; 23(5):466-9. PubMed ID: 2455472 [TBL] [Abstract][Full Text] [Related]
37. Animal Models of Self-Injurious Behavior: An Update. Devine DP Methods Mol Biol; 2019; 2011():41-60. PubMed ID: 31273692 [TBL] [Abstract][Full Text] [Related]
38. MR findings in the central nervous system of patients with a deletion of the long arm of chromosome 18(18q-). Becker LE AJNR Am J Neuroradiol; 1998 Feb; 19(2):399. PubMed ID: 9504507 [No Abstract] [Full Text] [Related]
39. The housekeeping gene hypoxanthine guanine phosphoribosyltransferase (HPRT) regulates multiple developmental and metabolic pathways of murine embryonic stem cell neuronal differentiation. Kang TH; Park Y; Bader JS; Friedmann T PLoS One; 2013; 8(10):e74967. PubMed ID: 24130677 [TBL] [Abstract][Full Text] [Related]
40. Myelination disturbance in a patient with hyperuricemia and hyperserotoninemia combined with 18q deletion syndrome. László A; Vörös E; Buga K; Horváth K; Mayer P; Osztovics M; Pávics L; Svekus A; Patterson MC Ideggyogy Sz; 2009 Nov; 62(11-12):413-7. PubMed ID: 20025132 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]