Ichizo Nishino
National Institute of Neuroscience
National Center of Neurology and Psychiatry (NCNP)
Tokyo
Japan
Name/email consistency: high
- Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. Nishino, I., Spinazzola, A., Hirano, M. Science. (1999)
- Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease). Nishino, I., Fu, J., Tanji, K., Yamada, T., Shimojo, S., Koori, T., Mora, M., Riggs, J.E., Oh, S.J., Koga, Y., Sue, C.M., Yamamoto, A., Murakami, N., Shanske, S., Byrne, E., Bonilla, E., Nonaka, I., DiMauro, S., Hirano, M. Nature. (2000)
- Autophagic vacuolar myopathies. Nishino, I. Curr. Neurol. Neurosci. Rep (2003)
- Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model. Malicdan, M.C., Noguchi, S., Hayashi, Y.K., Nonaka, I., Nishino, I. Nat. Med. (2009)