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33. A Golgi study of neuronal architecture in a genetic mouse model for Lesch-Nyhan disease. Mikolaenko I; Rao LM; Roberts RC; Kolb B; Jinnah HA Neurobiol Dis; 2005 Nov; 20(2):479-90. PubMed ID: 15908225 [TBL] [Abstract][Full Text] [Related]
34. [Investigation of a variant form of hypoxanthine-phosphoribosyl transferase in a family (author's transl)]. Willers I; Held KR; Singh S; Goedde HW Wien Klin Wochenschr; 1981 May; 93(10):329-31. PubMed ID: 7257414 [TBL] [Abstract][Full Text] [Related]
35. [Familial juvenile gout caused by partial HGPRT deficiency with neurologic manifestations; a variant of the Lesch-Nyhan syndrome?]. Laroche C; Cremer GA; Sereni D; Auscher C Bull Mem Acad R Med Belg; 1980; 135(3):219-31. PubMed ID: 7448460 [No Abstract] [Full Text] [Related]
37. [Lesch-Nyhan disease. Study of a new patient (author's transl)]. Carmena R; Nyhan WL; Ascaso J; Bakay B; Soriano J; Tebar J Med Clin (Barc); 1982 Jan; 78(2):59-64. PubMed ID: 7070131 [No Abstract] [Full Text] [Related]
38. An unexpected affected female patient in a classical Lesch-Nyhan family. De Gregorio L; Nyhan WL; Serafin E; Chamoles NA Mol Genet Metab; 2000 Mar; 69(3):263-8. PubMed ID: 10767182 [TBL] [Abstract][Full Text] [Related]
39. [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]