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Results: 1-5 |
Results: 5

Authors: Ohno, I Hosoya, T Gomi, H Ichida, K Okabe, H Hikita, M
Citation: I. Ohno et al., Serum uric acid and renal prognosis in patients with IgA nephropathy, NEPHRON, 87(4), 2001, pp. 333-339

Authors: Ichida, K Matsumura, T Sakuma, R Hosoya, T Nishino, T
Citation: K. Ichida et al., Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II, BIOC BIOP R, 282(5), 2001, pp. 1194-1200

Authors: Levartovsky, D Lagziel, A Sperling, O Liberman, U Yaron, M Hosoya, T Ichida, K Peretz, H
Citation: D. Levartovsky et al., XDH gene mutation is the underlying cause of classical xanthinuria: A second report, KIDNEY INT, 57(6), 2000, pp. 2215-2220

Authors: Ichida, K Ikeda, M Goto, K Ito, K
Citation: K. Ichida et al., Characterization of a palytoxin-induced non-selective cation channel in mouse megakaryocytes, JPN J PHARM, 81(2), 1999, pp. 200-208

Authors: Hikita, M Hosoya, T Ichida, K Okabe, H Saji, M Ohno, I Kuriyama, S Tomonari, H Hayashi, F Onouchi, K Fujimori, S Yamaoka, N Sakuma, R
Citation: M. Hikita et al., Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase manifesting as acute renal damage, INTERN MED, 37(11), 1998, pp. 945-949
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