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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 846797)

  • 1. [Pathogenesis and clinical manifestations of Lesch-Nyhan syndrome].
    Berger H; Zoch-Zwierz W
    Pediatr Pol; 1977 Mar; 52(3):335-41. PubMed ID: 846797
    [No Abstract]   [Full Text] [Related]  

  • 2. [Pathogenetic mechanisms and therapy of a subclinical form of Lesch-Nyhan syndrome].
    Semenova IA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(3):436-9. PubMed ID: 3705857
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inherited deficiency of hypoxanthine-guanine phosphoribosyltransferase in X-linked uric aciduria (the Lesch-Nyhan syndrome and its variants).
    Seegmiller JE
    Adv Hum Genet; 1976; 6():75-163. PubMed ID: 779428
    [No Abstract]   [Full Text] [Related]  

  • 4. [Clinical spectrum of hypoxanthine-guanine phosphoribosyltransferase deficiency: study of 12 cases].
    García Puig J; Mateos FA; Jiménez ML; Arcas J; Miranda ME; Oríz Vázquez J
    Med Clin (Barc); 1994 May; 102(18):681-7. PubMed ID: 8028417
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Membrane-associated HPRTase activity in hyperuricemic and Lesch-Nyhan syndrome cells.
    Yip LC; Xu YL; Balis ME
    Chin Med J (Engl); 1986 Nov; 99(11):927-30. PubMed ID: 3107935
    [No Abstract]   [Full Text] [Related]  

  • 7. Lesch-Nyhan syndrome in an Arab family. Detection and biochemical manifestation of heterozygosity.
    Shaltiel A; Katzuni E; Boer P; Zoref-Shani E; Sperling O
    Isr J Med Sci; 1981 Dec; 17(12):1169-73. PubMed ID: 7327917
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Metabolic aspects of the pathogenesis of hyperuricemia].
    Gutensohn W
    Verh Dtsch Ges Inn Med; 1986; 92():456-61. PubMed ID: 3811546
    [No Abstract]   [Full Text] [Related]  

  • 9. Clinical quiz. Lesch-Nyhan syndrome.
    Bhagat MM; Reid CJ
    Pediatr Nephrol; 1991 Nov; 5(6):758-60. PubMed ID: 1768590
    [No Abstract]   [Full Text] [Related]  

  • 10. Lesch-Nyhan Disease.
    Nyhan WL
    J Hist Neurosci; 2005 Mar; 14(1):1-10. PubMed ID: 15804753
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. [Teachings concerning congenital hyperuricemia. Lesch-Nyhan syndrome].
    Forette B
    Nouv Presse Med; 1973 Feb; 2(7):439-41. PubMed ID: 4688240
    [No Abstract]   [Full Text] [Related]  

  • 14. [Complete and partial deficiencies of hypoxanthine guanine phosphoribosyltransferase (HPRT)].
    Yamada Y
    Nihon Rinsho; 2003 Jan; 61 Suppl 1():288-93. PubMed ID: 12629733
    [No Abstract]   [Full Text] [Related]  

  • 15. Biochemical and genetic studies of an X-linked neurological disease (The Lesch-Nyhan syndrome).
    Seegmiller JE
    Harvey Lect; 1971; 65():175-92. PubMed ID: 4945433
    [No Abstract]   [Full Text] [Related]  

  • 16. [Enzymopathies as a cause of hyperuricemia].
    Eyman E; Kawenoki-Minc E
    Reumatologia; 1977; 15(3):375-81. PubMed ID: 929012
    [No Abstract]   [Full Text] [Related]  

  • 17. [Lesch-Nyhan syndrome: a new variant with hypoxanthine-guanine phosphoriboxyl transferase activity higher than the classical disease and detection of the heterozygote trait in the erythrocytes of the carrier].
    Hernández Nieto L; Nyhan WL; Page T; Cubillo Ferreira G; Rodríguez Fernández M; González García T; Cabrera de León A; Santolaria Fernández FJ
    Med Clin (Barc); 1985 Jan; 84(2):68-71. PubMed ID: 3974350
    [No Abstract]   [Full Text] [Related]  

  • 18. Molecular genetics of hypoxanthine-guanine phosphoribosyltransferase deficiency in man.
    Wilson JM; Kelley WN
    Arch Intern Med; 1985 Oct; 145(10):1895-1900. PubMed ID: 3899038
    [No Abstract]   [Full Text] [Related]  

  • 19. [Hypoxanthine guanine phosphoribosyl transferase deficiency; Lesch-Nyhan syndrome].
    Ogasawara N
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):601-5. PubMed ID: 3270871
    [No Abstract]   [Full Text] [Related]  

  • 20. Prenatal diagnosis of Lesch-Nyhan syndrome by purine analysis of amniotic fluid and cordocentesis.
    Mateos FA; Puig JG; Ramos TH; Jiménez ML; Romera NM; González AG
    Adv Exp Med Biol; 1991; 309B():47-50. PubMed ID: 1781404
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.