BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 857624)

  • 1. Purine excretion in complete adenine phosphoribosyltransferase deficiency: effect of diet and allopurinol therapy.
    Simmonds HA; Van Acker KJ; Cameron JS; McBurney A
    Adv Exp Med Biol; 1977; 76B():304-11. PubMed ID: 857624
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Complete deficiency of adenine phosphoribosyltransferase. Report of a family.
    Van Acker KJ; Simmonds HA; Potter C; Cameron JS
    N Engl J Med; 1977 Jul; 297(3):127-32. PubMed ID: 865583
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spectrum of 2,8-dihydroxyadenine urolithiasis in complete APRT deficiency.
    Simmonds HA; Barratt TM; Webster DR; Sahota A; Van Acker KJ; Cameron JS; Dillon M
    Adv Exp Med Biol; 1980; 122A():337-41. PubMed ID: 7424654
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 2,8-Dihydroxyadeninuria--or when is a uric acid stone not a uric acid stone?
    Simmonds HA
    Clin Nephrol; 1979 Nov; 12(5):195-7. PubMed ID: 389507
    [No Abstract]   [Full Text] [Related]  

  • 5. Adenine phosphoribosyltransferase deficiency: a case diagnosed by GC-MS identification of 2,8-dihydroxyadenine in urinary crystals.
    Christensen E; Brandt NJ; Laxdal T
    J Inherit Metab Dis; 1987; 10(2):187-94. PubMed ID: 3116337
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complete deficiency of adenine phosphoribosyltransferase: a third case presenting as renal stones in a young child.
    Barratt TM; Simmonds HA; Cameron JS; Potter CF; Rose GA; Arkell DG; Williams DI
    Arch Dis Child; 1979 Jan; 54(1):25-31. PubMed ID: 420519
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Complete adenine phosphoribosyltransferase (APRT) deficiency in two siblings: report of a new case.
    Cartier P; Hamet M; Vincens A; Perignon JL
    Adv Exp Med Biol; 1980; 122A():343-8. PubMed ID: 7424655
    [No Abstract]   [Full Text] [Related]  

  • 8. Adenine phosphoribosyltransferase deficiency: 2,8-dihydroxyadenine urolithiasis in a 48-year-old woman.
    Usenius JP; Ruopuro ML; Usenius R
    Br J Urol; 1988 Dec; 62(6):521-4. PubMed ID: 3219508
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 2,8-dihydroxyadenine urolithiasis: review of the literature and report of a case in the United States.
    Witten FR; Morgan JW; Foster JG; Glenn JF
    J Urol; 1983 Nov; 130(5):938-42. PubMed ID: 6632104
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Purine and pyrimidine metabolism in hereditary orotic aciduria: some unexpected effects of allopurinol.
    Simmonds HA; Webster DR; Becroft DM; Potter CF
    Eur J Clin Invest; 1980 Aug; 10(4):333-9. PubMed ID: 6775961
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 2,8-Dihydroxyadenine urolithiasis: report of an adult case in the United States.
    Manyak MJ; Frensilli FJ; Miller HC
    J Urol; 1987 Feb; 137(2):312-4. PubMed ID: 3806829
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A rare enzyme deficiency causing formation of 2,8-dihydroxyadenine (purine body) calculi.
    Szönyi P; Berényi M; Tóth J
    Int Urol Nephrol; 1985; 17(3):231-3. PubMed ID: 4086237
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A new metabolic disease: the complete deficit of adenine phosphoribosyltransferase and lithiasis of 2,8-dihydroxyadenine].
    Cartier P; Hamet M; Hamburger J
    C R Acad Hebd Seances Acad Sci D; 1974 Sep; 279(10):883-6. PubMed ID: 4219298
    [No Abstract]   [Full Text] [Related]  

  • 14. [Uric acid stones in children. Identification and therapy of a newly detected defect of adenine-phosphoribosyltransferase (author's transl)].
    Simmonds HA
    MMW Munch Med Wochenschr; 1979 Dec; 121(49):1654-6. PubMed ID: 118367
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Purine metabolism and immunodeficiency: urinary purine excretion as a diagnostic screening test in adenosine deaminase and purine nucleoside phosphorylase deficiency.
    Simmonds HA; Sahota A; Potter CF; Cameron JS
    Clin Sci Mol Med; 1978 May; 54(5):579-84. PubMed ID: 108044
    [No Abstract]   [Full Text] [Related]  

  • 16. Distribution of patients with 2,8-dihydroxyadenine urolithiasis and adenine phosphoribosyltransferase deficiency in Japan.
    Kamatani N; Sonoda T; Nishioka K
    J Urol; 1988 Dec; 140(6):1470-2. PubMed ID: 3193517
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [2,8-Dihydroxyadeninuria: 2.8-dihydroxyadenine crystals in urinary sediment in patients with adenine-phosphoribosyltransferase deficiency].
    Noro T; Ogiwara M; Okamura M
    Dtsch Med Wochenschr; 1982 Dec; 107(49):1887-90. PubMed ID: 7140571
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hereditary deficiency in adenine phosphoribosyltransferase: a metabolic cause of urinary lithiasis in children (author's transl)].
    Cartier P; Hamet M; Perignon JL
    Nouv Presse Med; 1980 Jun; 9(25):1767-70. PubMed ID: 6892958
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Phosphoribosyltransferase (APRT) deficiency--molecular and clinical aspects of dihydroxyadeninuria].
    Safranow K
    Postepy Hig Med Dosw; 1998; 52(1):89-104. PubMed ID: 9608233
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new family with APRT partial deficiency: studies on purine and uric acid metabolism.
    Ciompi ML; Bazzichi L; Pasero G; Mariani G
    Adv Exp Med Biol; 1986; 195 Pt A():47-50. PubMed ID: 3524139
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.