ACTH therapy for West syndrome with severe hemophilia A

by Kubota, Kazuo, Kinomura, Yoriko, Yamamoto, Takahiro, Ozeki, Michio, Kawamoto, Minako, Kawamoto, Norio, Fukao, Toshiyuki
Published 2016

A structural mapping of mutations causing succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency

by Shafqat, Naeem, Kavanagh, Kate L., Sass, Jörn Oliver, Christensen, Ernst, Fukao, Toshiyuki, Lee, Wen Hwa, Oppermann, Udo, Yue, Wyatt W.
Published 2013

Application of multiplex ligation-dependent probe amplification, and identification of a heterozygous Alu-associated deletion and a uniparental disomy of chromosome 1 in two patien...

by AOYAMA, YUKA, YAMAMOTO, TOSHIYUKI, SAKAGUCHI, NAOMI, ISHIGE, MIKA, TANAKA, TOJU, ICHIHARA, TOMOKO, OHARA, KATSUAKI, KOUZAN, HIROKO, KINOSADA, YASUTOMI, FUKAO, TOSHIYUKI
Published 2015

Impact of enzyme replacement therapy and hematopoietic stem cell therapy on growth in patients with Hunter syndrome

by Patel, Pravin, Suzuki, Yasuyuki, Tanaka, Akemi, Yabe, Hiromasa, Kato, Shunichi, Shimada, Tsutomu, Mason, Robert W., Orii, Kenji E., Fukao, Toshiyuki, Orii, Tadao, Tomatsu, Shunji
Published 2014