M. Yonekawa

A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 1998, Journal of the Neurological Sciences.

Loss of wild‐type carrier‐mediated L‐carnitine transport activity in hepatocytes of juvenile visceral steatosis mice

K. Miyamoto, J. Nezu, A. Oku, 1999, Hepatology.

Regional Cerebral Blood Flow in Depression

M. Yonekawa, T. Kanaya, 1990, The Japanese journal of psychiatry and neurology.

A Case of Hereditary Ceruloplasmin Deficiency with Iron Deposition in the Brain Associated with Chorea, Dementia, Diabetes mellitus and Retinal Pigmentation: Administration of Fresh-Frozen Human Plasma

M. Ohta, M. Yonekawa, T. Okabe, 1999, European Neurology.