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Kimiyoshi Ichida

Division of Kidney and Hypertension

Jikei University School of Medicine

Tokyo

Japan

[email]@jikei.ac.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Division of Kidney and Hypertension, Jikei University School of Medicine, Tokyo, Japan. 2006
  • Division of Nephrology and Hypertension, Department of Internal Medicine, Jikei University School of Medicine, 3-25-8 Nishishimbashi, Japan. 2001 - 2004

References

  1. 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) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
 
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