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2. [Self mutilation behavior and uric acid metabolism disorders in an adult (Lesch-Nyhan syndrome?)]. Eyssette M; Setiey A; Aimard G; Devic M Rev Neurol (Paris); 1972 Feb; 126(2):144-9. PubMed ID: 4654781 [No Abstract] [Full Text] [Related]
3. [Biochemical and immunological studies of hypoxanthine-guanine phosphoribosyltransferase in erythrocytes of Lesch-Nyhan patients (author's transl)]. Müller MM; Stemberger H Wien Klin Wochenschr; 1974 Mar; 86(5):127-31. PubMed ID: 4820571 [No Abstract] [Full Text] [Related]
4. [Hyperuricemia and disorders of the central nervous system. Report of a case of Lesch-Nyhan syndrome]. Teja Medina M; Blanco de la Mora E Prensa Med Mex; 1977; 42(11-12):522-8. PubMed ID: 614549 [No Abstract] [Full Text] [Related]
5. The Lesch-Nyhan syndrome. Nyhan WL Dev Med Child Neurol; 1978 Jun; 20(3):376-80. PubMed ID: 307504 [No Abstract] [Full Text] [Related]
6. The Lesch-Nyhan syndrome. Nyhan WL Annu Rev Med; 1973; 24():41-60. PubMed ID: 4575865 [No Abstract] [Full Text] [Related]
8. 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]
9. The Lesch-Nyhan syndrome: report of three cases. Wood MH; Fox RM; Vincent L; Reye C; O'Sullivan WJ Aust N Z J Med; 1972 Feb; 2(1):57-64. PubMed ID: 4502719 [No Abstract] [Full Text] [Related]
16. In vitro effects of magnesium ions on mutant cells from patients with the Lesch-Nyhan syndrome. Benke PJ; Hebert A; Herrick N N Engl J Med; 1973 Aug; 289(9):446-50. PubMed ID: 4763410 [No Abstract] [Full Text] [Related]
17. 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]
18. [Lesch-Nyhan syndrome]. Horváth M; Fekete M; Gábriel I Orv Hetil; 1974 Dec; 115(52):3102-4. PubMed ID: 4437927 [No Abstract] [Full Text] [Related]
19. Erythrocyte PRPP concentrations in heterozygotes for HGPRTase deficiency. Gordon RB; Thompson L; Emmerson BT Adv Exp Med Biol; 1973; 41():291-5. PubMed ID: 4791203 [No Abstract] [Full Text] [Related]
20. An atypical case of hypoxanthine-guanine phosphoribosyltransferase deficiency (Lesch-Nyhan syndrome). I. Clinical studies. Geerdink RA; de Vries WH; Willemse J; Oei TL; de Bruyn CH Clin Genet; 1973; 4(4):348-52. PubMed ID: 4747811 [No Abstract] [Full Text] [Related] [Next] [New Search]