Kunihiro Yoshida

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

Kunihiro Yoshida, Kenichi Furihata, Shin’ichi Takeda et al. · Nature Genetics · 1995 · 461 citations

Ceruloplasmin Gene, Genetics, Pathogenesis +4

Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease

Akira Kinoshita, Takashi Saito, Hiroaki Tomita et al. · Nature Genetics · 2000 · 245 citations

Translational Biology, Genetic Disorder, Receptor Tyrosine Kinase +5

Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a japanese family

Hiroshi Morita, Shu‐ichi Ikeda, Kanji Yamamoto et al. · Annals of Neurology · 1995 · 244 citations

Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with <i><scp>CSF</scp>1R</i> mutation

Takuya Konno, Kunihiro Yoshida, Toshiki Mizuno et al. · European Journal of Neurology · 2016 · 172 citations · Full text

An X-ray structural study of human ceruloplasmin in relation to ferroxidase activity

Peter F. Lindley, G.L. Card, I. Zaitseva et al. · JBIC Journal of Biological Inorganic Chemistry · 1997 · 128 citations

Human Ceruloplasmin, Biomolecular Engineering, Biochemistry +1