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 *

308 related articles for article (PubMed ID: 4713272)

  • 1. [Self mutilation of the lower lip, associated with athetosis and oligophrenia without purine metabolism disorder ("pseudo Lesch-Nyhan syndrome")].
    Meigel W; Braun-Falco O
    Hautarzt; 1973 Apr; 24(4):158-60. PubMed ID: 4713272
    [No Abstract]   [Full Text] [Related]  

  • 2. Clinical and therapeutic aspects of the Lesch-Nyhan syndrome in Japanese children.
    Mizuno T; Segawa M; Kurumada T; Maruyama H; Onisawa J
    Neuropadiatrie; 1970 Aug; 2(1):38-52. PubMed ID: 5538093
    [No Abstract]   [Full Text] [Related]  

  • 3. Detection of females heterozygous for the Lesch-Nyhan mutation by 8-azaguanine-resistant growth of cultured fibroblasts.
    Felix JS; DeMars R
    J Lab Clin Med; 1971 Apr; 77(4):596-604. PubMed ID: 4252001
    [No Abstract]   [Full Text] [Related]  

  • 4. Hyperuricemia. Case presentation.
    J Ark Med Soc; 1971 Dec; 68(7):212-6. PubMed ID: 4256879
    [No Abstract]   [Full Text] [Related]  

  • 5. Lesch-Nyhan syndrome.
    Arima M; Aoki N; Ono K
    Paediatr Univ Tokyo; 1970 Dec; 18():25-31. PubMed ID: 5514644
    [No Abstract]   [Full Text] [Related]  

  • 6. Detection of the heterozygote in Lesch-Nyhan disease by hair-root analysis.
    Silvers DN; Cox RP; Balis ME; Dancis J
    N Engl J Med; 1972 Feb; 286(8):390-5. PubMed ID: 4333083
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Preventive control of the Lesch-Nyhan syndrome.
    Van Heeswijk PJ; Blank CH; Seegmiller JE; Jacobson CB
    Obstet Gynecol; 1972 Jul; 40(1):109-13. PubMed ID: 5044927
    [No Abstract]   [Full Text] [Related]  

  • 9. Biochemistry of the X-linked uric aciduria--enzyme defect and its genetic variants.
    Kelley WN
    Arch Intern Med; 1972 Aug; 130(2):199-206. PubMed ID: 5050555
    [No Abstract]   [Full Text] [Related]  

  • 10. Clinical features of the Lesch-Nyhan syndrome.
    Nyhan WL
    Arch Intern Med; 1972 Aug; 130(2):186-92. PubMed ID: 5050553
    [No Abstract]   [Full Text] [Related]  

  • 11. An approach to the control of PRT deficiency through antenatal diagnosis.
    Fujimoto WY
    Arch Intern Med; 1972 Aug; 130(2):207-11. PubMed ID: 5050556
    [No Abstract]   [Full Text] [Related]  

  • 12. Lesch-Nyhan syndrome. Summary of clinical features.
    Nyhan WL
    Fed Proc; 1968; 27(4):1034-41. PubMed ID: 5658469
    [No Abstract]   [Full Text] [Related]  

  • 13. Diagnosis and treatment of the Lesch-Nyhan syndrome.
    Crawhall JC; Henderson JF; Kelley WN
    Pediatr Res; 1972 May; 6(5):504-13. PubMed ID: 4558815
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Alteration of purine control mechanisms in patients with the Lesch-Nyhan mutation.
    Benke PJ
    Wis Med J; 1971 Jul; 70(7):174-5. PubMed ID: 5560233
    [No Abstract]   [Full Text] [Related]  

  • 16. Hyperuricosuria and central nervous system dysfunction.
    Berman PH; Balis ME; Krakoff IH; Dancis J
    Trans Am Neurol Assoc; 1967; 92():138-42. PubMed ID: 5634009
    [No Abstract]   [Full Text] [Related]  

  • 17. A screening technique for the Lesch-Nyhan syndrome.
    Jenkins EC
    J Pediatr; 1971 Oct; 79(4):663-6. PubMed ID: 5094259
    [No Abstract]   [Full Text] [Related]  

  • 18. Further studies of the enzyme composition of mutant cells in X-linked uric aciduria.
    Sweetman L; Nyhan WL
    Arch Intern Med; 1972 Aug; 130(2):214-20. PubMed ID: 5065734
    [No Abstract]   [Full Text] [Related]  

  • 19. A method for the prenatal diagnosis of the Lesch-Nyhan syndrome using fresh amniotic cells.
    Berman PH; Balis ME; Dancis J
    Trans Am Neurol Assoc; 1969; 94():222-4. PubMed ID: 5374441
    [No Abstract]   [Full Text] [Related]  

  • 20. Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome.
    Arnold WJ; Meade JC; Kelley WN
    J Clin Invest; 1972 Jul; 51(7):1805-12. PubMed ID: 4624352
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.