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132 related items for PubMed ID: 1868258

  • 1. A new method for the determination of adenine phosphoribosyltransferase activity in human erythrocytes by reversed phase high performance liquid chromatography.
    Kojima T, Nishina T, Kitamura M, Yamanak H, Nishioka K.
    Biomed Chromatogr; 1991 Mar; 5(2):57-61. PubMed ID: 1868258
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  • 2. Screening for adenine and hypoxanthine phosphoribosyltransferase deficiencies in human erythrocytes by high-performance liquid chromatography.
    Sakuma R, Nishina T, Kitamura M, Yamanaka H, Kamatani N, Nishioka K.
    Clin Chim Acta; 1987 Dec; 170(2-3):281-9. PubMed ID: 3436062
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  • 3. A high performance liquid chromatographic assay for AMP-deaminase activity in the erythrocytes of healthy subjects and patients with inherited purine disorders.
    Smolenski RT, Montero C, Rodgers AV, Simmonds HA.
    Biomed Chromatogr; 1991 Jul; 5(4):171-4. PubMed ID: 1912725
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  • 4. Scanning electron microscopy of 2,8-dihydroxyadenine crystals and stones.
    Winter P, Hesse A, Klocke K, Schaefer RM.
    Scanning Microsc; 1993 Sep; 7(3):1075-80. PubMed ID: 8146608
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  • 5. High-performance liquid chromatographic method for simultaneous screening of the deficiencies of APRT and HPRT.
    Nishina T, Sakuma R, Kojima T, Kiyamura M, Kamatani N, Nishioka K.
    Adv Exp Med Biol; 1989 Sep; 253A():59-65. PubMed ID: 2483031
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  • 8. Complete deficiency of adenine phosphoribosyltransferase: report of a family.
    Van Acker KJ, Simmonds HA, Cameron JS.
    Adv Exp Med Biol; 1977 Sep; 76A():295-305. PubMed ID: 855710
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  • 9. Partial and complete adenine phosphoribosyltransferase deficiency associated with 2,8-dihydroxyadenine urolithiasis: kinetic and immunochemical properties of APRT.
    Abe S, Hayasaka K, Narisawa K, Tada K, Okada G, Koyama H, Kurosu S, Kudoh M, Matsushita K.
    Enzyme; 1987 Sep; 37(4):182-8. PubMed ID: 2440671
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  • 11. [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 07; 9(25):1767-70. PubMed ID: 6892958
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  • 12. Adenine phosphoribosyltransferase deficiency: its inheritance and occurrence in a female with gout and renal disease.
    Emmerson BT, Gordon RB, Thompson L.
    Aust N Z J Med; 1975 Oct 07; 5(5):440-6. PubMed ID: 1061547
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  • 13. [Erythrocyte purine phosphoribosyltransferase activity in girls with the Lesch-Nyhan syndrome].
    Aleksandrova LA, Shaposhnikov AM.
    Vopr Med Khim; 1981 Oct 07; 27(4):488-92. PubMed ID: 7293080
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  • 16. Simultaneous determination of 16 purine derivatives in urinary calculi by gradient reversed-phase high-performance liquid chromatography with UV detection.
    Safranow K, Machoy Z.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2005 May 25; 819(2):229-35. PubMed ID: 15833286
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  • 19. 2,8-Dihydroxyadenine urolithiasis due to partial deficit in adenine phosphoribosyltransferase: a case report.
    Katsuoka Y, Miyakita H, Shiramizu M, Iwagaki H, Ikeda T.
    Hinyokika Kiyo; 1992 May 25; 38(5):573-7. PubMed ID: 1609669
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  • 20. A mutant adenine phosphoribosyltransferase in 2,8-dihydroxyadenine urolithiasis.
    Nishida Y, Hirano S, Miyamoto T.
    Arch Intern Med; 1986 Oct 25; 146(10):2068-70. PubMed ID: 3767554
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