Kimiyoshi Ichida
Division of Kidney and Hypertension
Jikei University School of Medicine
Tokyo
Japan
Name/email consistency: high
- A Turkish case with molybdenum cofactor deficiency. Ichida, K., Aydin, H.I., Hosoyamada, M., Kalkanoglu, H.S., Dursun, A., Ohno, I., Coskun, T., Tokatli, A., Shibasaki, T., Hosoya, T. Nucleosides. Nucleotides. Nucleic. Acids (2006)
- Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. Ichida, K., Hosoyamada, M., Hisatome, I., Enomoto, A., Hikita, M., Endou, H., Hosoya, T. J. Am. Soc. Nephrol. (2004)
- Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II. Ichida, K., Matsumura, T., Sakuma, R., Hosoya, T., Nishino, T. Biochem. Biophys. Res. Commun. (2001)