Morita, Hiroshi

A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans

Yoshida, K., Furihata, K., Takeda, S., Nakamura, A., Yamamoto, K., Morita, H., Hiyamuta, S., Ikeda, S.-I., Shimizu, N., & Yanagisawa, N. (1995) · Nature Genetics

Neurological diseases and metabolismIron Metabolism and Disorders

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Combination therapy with intravitreal tissue plasminogen activator and ranibizumab for subfoveal type 2 choroidal neovascularization

Kachi, I., Yasukawa, T., Kato, A., Takase, N., Morita, H., Kubota, A., Hirano, Y., Uemura, A., & Ogura, Y. (2016) · Japanese Journal of Ophthalmology

Retinal Diseases and TreatmentsRetinal and Macular Surgery

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