BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 7070131)

  • 1. [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]  

  • 2. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Lesch-Nyhan syndrome with total deficiency of the enzyme hypoxanthine phosphoribosyltransferase].
    Pascual-Castroviejo I; Vélez A; García Puig J; López Jiménez M
    Neurologia; 1986; 1(1):44-5. PubMed ID: 3274108
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 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. Lesch-Nyhan syndrome: biochemical characterization of a case with attenuated behavioral manifestation.
    Fattal A; Spirer Z; Zoref-Shani E; Sperling O
    Enzyme; 1984; 31(1):55-60. PubMed ID: 6201351
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Eighteen novel mutations in patients with Lesch-Nyhan syndrome or partial hypoxanthine phosphoribosyltransferase deficiency.
    Willers I; Bolz H; Wehnert M; Gal A
    J Inherit Metab Dis; 1999 Oct; 22(7):845-6. PubMed ID: 10518289
    [No Abstract]   [Full Text] [Related]  

  • 8. [Varience of phenotypic expression in hereditary neurological disorders (author's transl)].
    Arima M
    No To Shinkei; 1979 May; 31(5):439-43. PubMed ID: 486265
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. [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]  

  • 11. [A family of hypoxanthine-guanine phosphoribosyl transferase deficiency without neurological disorders (author's transl)].
    Toyo-Oka T; Akaoka I; Nishizawa T; Yoshimura T; Nishida Y
    Nihon Naika Gakkai Zasshi; 1975 Jan; 64(1):38-43. PubMed ID: 1236912
    [No Abstract]   [Full Text] [Related]  

  • 12. HPRT deficiency in a two-month-old child presenting acute renal failure and gout with a new deletion of two bases in exon 3 of the HPRT gene.
    Zamora A; Escárcega RO; Vazquez R; Zamora A; O'Neill JP
    Arch Med Res; 2007 May; 38(4):460-2. PubMed ID: 17416296
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Molecular analysis of the mutations in five unrelated patients with the Lesch Nyhan syndrome.
    Marcus S; Christensen E; Malm G
    Hum Mutat; 1993; 2(6):473-7. PubMed ID: 8111415
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. [Lesch-Nyhan syndrome].
    Akaoka I
    Nihon Rinsho; 1975 Feb; 33(2):340-4. PubMed ID: 1170375
    [No Abstract]   [Full Text] [Related]  

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

  • 18. 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; 24(3):199-200. PubMed ID: 477417
    [No Abstract]   [Full Text] [Related]  

  • 19. [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]  

  • 20. [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]  

    [Next]    [New Search]
    of 5.