Makoto Yoshino

Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

Jun‐ichi Nezu, Ikumi Tamai, Asuka Oku et al. · Nature Genetics · 1999 · 551 citations

Sodium Homeostasis, Genetics, Inherited Metabolic Disease +3

Phase II study of CPT-11, a new camptothecin derivative, in metastatic colorectal cancer. CPT-11 Gastrointestinal Cancer Study Group.

Y. Shimada, Makoto Yoshino, A Wakui et al. · Journal of Clinical Oncology · 1993 · 392 citations

Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency

Haruo Shintaku, Shigeo Kure, Toshihiro Ohura et al. · Zhongguo dangdai erke zazhi · 2005 · 254 citations

Biosynthesis, Biochemical Genetics, Biochemistry +1

Dry eye after haematopoietic stem cell transplantation

Yoko Ogawa, S. Okamoto, Masatoshi Wakui et al. · British Journal of Ophthalmology · 1999 · 244 citations · Full text

<i>MLL2</i> and <i>KDM6A</i> mutations in patients with Kabuki syndrome

Noriko Miyake, Eriko Koshimizu, Nobuhiko Okamoto et al. · American Journal of Medical Genetics Part A · 2013 · 174 citations · Full text