T. Okazaki

A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron.

M. Yano, H. Hayashi, S. Wakusawa, 2005, Internal medicine.

Transforming genes and chromosome aberrations in therapy-related leukemia and myelodysplastic syndrome

K. Inokuchi, N. Amuro, K. Dan, 1991, Annals of Hematology.

A case of intractable diarrhea firmly suspected to have autoimmune enteropathy

Hatsumi Yamamoto, K. Sugiyama, T. Okazaki, 1994, Acta paediatrica Japonica : Overseas edition.

Hemoglobin Sendagi (β42 Phe↠Val): A New Unstable Hemoglobin Variant Having an Amino Acid Substitution at Cd1 of the β-Chain

K. Ogata, Y. Nozawa, A. Kajita, 1986 .