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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

184 related items for PubMed ID: 6440462

  • 1. [Sex-related neurologic diseases. Hunter's disease. Lesch-Nyhan syndrome].
    Nieto Barrera M.
    An Esp Pediatr; 1984 Oct; 21 Suppl 20():47-50. PubMed ID: 6440462
    [No Abstract] [Full Text] [Related]

  • 2. [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 Oct; 135(3):219-31. PubMed ID: 7448460
    [No Abstract] [Full Text] [Related]

  • 3. [Lesch-Nyhan syndrome].
    Hernández Nieto L.
    Med Clin (Barc); 1994 May 14; 102(18):699-700. PubMed ID: 8028420
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. What syndrome is this? Lesch-Nyhan syndrome.
    Schepis C, Greco D, Siragusa M, Romano C.
    Pediatr Dermatol; 1996 May 14; 13(2):169-70. PubMed ID: 9122079
    [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 14; 3(3):235-40. PubMed ID: 8485579
    [Abstract] [Full Text] [Related]

  • 7. Advances in the study of inherited metabolic disease.
    Gibbs DA.
    J Inherit Metab Dis; 1989 Mar 14; 12(2):240-6. PubMed ID: 2569050
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. [A Japanese family with Lesch-Nyhan syndrome resulting from a new point mutation in hypoxanthine-guanine phosphoribosyltransferase gene].
    Maruta K, Ohi T, Yamada Y, Goto H, Ogasawara N, Matsukura S.
    No To Shinkei; 1997 Nov 14; 49(11):1009-13. PubMed ID: 9396032
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Lesch-Nyhan syndrome. Repository identification Nos. GM-2290, 2291, 2292, 2338, 3115, 3116, and 3117.
    Tischfield J, Schafer IA, Dickerman LH, Trill J, Mulivor RA, Greene AE, Coriell LL.
    Cytogenet Cell Genet; 1979 Nov 14; 24(3):199-200. PubMed ID: 477417
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Neurocognitive functioning in Lesch-Nyhan disease and partial hypoxanthine-guanine phosphoribosyltransferase deficiency.
    Schretlen DJ, Harris JC, Park KS, Jinnah HA, del Pozo NO.
    J Int Neuropsychol Soc; 2001 Nov 14; 7(7):805-12. PubMed ID: 11771623
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [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
    [No Abstract] [Full Text] [Related]

  • 19. Germline mosaicism complicates molecular diagnosis of Lesch-Nyhan syndrome.
    Willers I.
    Prenat Diagn; 2004 Sep 25; 24(9):737-40. PubMed ID: 15386453
    [Abstract] [Full Text] [Related]

  • 20. Hyperuricaemia associated with 18q deletion. Atypical Lesch-Nyhan syndrome?
    Laszlo A, Osztovics M, Dallmann L, Mattyus A.
    Ann Genet; 1981 Sep 25; 24(1):17-20. PubMed ID: 6971610
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.