Functional Analysis of RUNX2 Mutations in Japanese Patients with Cleidocranial Dysplasia Demonstrates Novel Genotype-Phenotype Correlations

Por Yoshida, Taketoshi, Kanegane, Hirokazu, Osato, Motomi, Yanagida, Masatoshi, Miyawaki, Toshio, Ito, Yoshiaki, Shigesada, Katsuya
Publicado em 2002

Successful treatment of hemochromatosis with renal tubular dysgenesis in a preterm infant

Por Koura, Uta, Horikawa, Shinjiro, Okabe, Mako, Kawasaki, Yukako, Makimoto, Masami, Mizuta, Koichi, Yoshida, Taketoshi
Publicado no Clin Case Rep (2015)

Neonatal acute megakaryoblastic leukemia mimicking congenital neuroblastoma

Por Kawasaki, Yukako, Makimoto, Masami, Nomura, Keiko, Hoshino, Akihiro, Hamashima, Takeru, Hiwatari, Mitsuteru, Nakazawa, Atsuko, Takita, Junko, Yoshida, Taketoshi, Kanegane, Hirokazu
Publicado no Clin Case Rep (2015)