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Journal Abstract Search

208 related items for PubMed ID: 2255060

  • 1. [Sideroblastic anemia associated with adenine phosphoribosyltransferase deficiency].
    Mita M, Midorikawa J, Kokubun K, Uchida T.
    Rinsho Ketsueki; 1990 Oct; 31(10):1701-5. PubMed ID: 2255060
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  • 4. [A case of adenine phosphoribosyltransferase (APRT) deficiency discovered by urine examination].
    Konishi N, Takeshita K, Yasui H.
    Nihon Jinzo Gakkai Shi; 1994 Oct; 36(10):1191-5. PubMed ID: 7815752
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  • 5. 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; 38(5):573-7. PubMed ID: 1609669
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  • 6. Clinical, biochemical and molecular diagnosis of a compound homozygote for the 254 bp deletion-8 bp insertion of the APRT gene suffering from severe renal failure.
    Di Pietro V, Perruzza I, Amorini AM, Balducci A, Ceccarelli L, Lazzarino G, Barsotti P, Giardina B, Tavazzi B.
    Clin Biochem; 2007 Jan; 40(1-2):73-80. PubMed ID: 17126311
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  • 7. [The first case of adenine phosphoribosyltransferase deficiency with APRT*Q0 (M1I) mutation in Japan].
    Ikeda H, Watanabe T, Fujimoto Y, Yamamoto S, Hosaki I, Isoyama K, Kawano S, Chiba M.
    Hinyokika Kiyo; 2012 Jul; 58(7):15-9. PubMed ID: 22988602
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  • 8. [Two siblings with 2,8-dihydroxyadenine urolithiasis].
    Kambayashi T, Nakanishi T, Suzuki K, Fujita K, Tajima A, Kawabe K.
    Hinyokika Kiyo; 1994 Dec; 40(12):1097-101. PubMed ID: 7863862
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  • 9. [The first case of adenine phosphoribosyltransferase deficiency with APRT Q0 (M1V) mutation in Japan].
    Ikeda H, Watanabe T, Fujimoto Y, Yamamoto S, Hosaki I, Isoyama K, Kawano S, Chiba M.
    Hinyokika Kiyo; 2011 Jan; 57(1):15-9. PubMed ID: 21304254
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  • 10. [A case of right ureteral stone with complete deficiency of adenine phosphoribosyltransferase].
    Ito T, Sugimoto T, Maekawa M, Horii A, Yasumoto R.
    Hinyokika Kiyo; 1985 Aug; 31(8):1453-8. PubMed ID: 4083207
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  • 13. Adenine phosphoribosyltransferase deficiency with renal deposition of 2,8-dihydroxyadenine leading to nephrolithiasis and chronic renal failure.
    Fye KH, Sahota A, Hancock DC, Gelb AB, Chen J, Sparks JW, Sibley RK, Tischfield JA.
    Arch Intern Med; 1993 Mar 22; 153(6):767-70. PubMed ID: 8447714
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  • 14. [Sideroblastic anemia preceded by essential thrombocythemia with 20q- chromosome abnormality].
    Yamada K, Nakamaki T, Yokoyama A, Hino K, Tomoyasu S, Sakurai M, Tsuruoka N.
    Rinsho Ketsueki; 1993 Sep 22; 34(9):1027-32. PubMed ID: 8230746
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  • 16. [Post-gastrectomized vitamin B12 deficient anemia with marked leukoerythroblastosis and ringed sideroblasts].
    Yoshimoto S, Takeuchi M, Tada A, Taguchi H, Manabe T.
    Rinsho Ketsueki; 1992 May 22; 33(5):688-93. PubMed ID: 1630022
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  • 19. [A case of 2,8-dihydroxyadenine stone with a partial deficiency of adenine phosphoribosyltransferase].
    Kitami K, Kinoshita Y, Hosaka M.
    Hinyokika Kiyo; 1990 Jan 22; 36(1):73-6. PubMed ID: 2408267
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  • 20. Erythroid precursor cells in primary acquired and secondary sideroblastic anemia.
    Takaku F, Mizoguchi H, Suda T, Kubota K, Miura Y.
    Exp Hematol; 1980 Jan 22; 8 Suppl 8():225-34. PubMed ID: 6962069
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