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Journal Abstract Search

174 related items for PubMed ID: 3330841

  • 1. Lesch-Nyhan syndrome: mutation, prevention, and therapy.
    Caskey CT.
    Res Publ Assoc Res Nerv Ment Dis; 1987; 65():187-94. PubMed ID: 3330841
    [No Abstract] [Full Text] [Related]

  • 2. Lesch-Nyhan disease.
    Nyhan WL.
    Nucleosides Nucleotides Nucleic Acids; 2008 Jun; 27(6):559-63. PubMed ID: 18600504
    [Abstract] [Full Text] [Related]

  • 3. Lesch-Nyhan syndrome: a novel complex mutation with severe phenotype.
    Gucev Z, Koceva S, Marinaki A, Fairbanks L, Kirovski I, Tasic V.
    Clin Genet; 2010 Sep; 78(3):296-7. PubMed ID: 20695874
    [No Abstract] [Full Text] [Related]

  • 4. Lesch-Nyhan syndrome. Engineering mutant mice.
    Hogan B.
    Nature; 2010 Sep; 326(6110):240-1. PubMed ID: 3469525
    [No Abstract] [Full Text] [Related]

  • 5. HPRT: gene structure, expression, and mutation.
    Stout JT, Caskey CT.
    Annu Rev Genet; 1985 Sep; 19():127-48. PubMed ID: 3909940
    [No Abstract] [Full Text] [Related]

  • 6. 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
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  • 7. [Lesch-Nyhan disease studied in intact fibroblasts].
    Lartigau MT, Martínez A, Bakay B, Page T, Nyhan WL.
    An Esp Pediatr; 1983 May; 18(5):394-8. PubMed ID: 6614674
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  • 16. [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 25; 78(2):59-64. PubMed ID: 7070131
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  • 19. [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 25; 17(1):60-4. PubMed ID: 7137725
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