Molecular Biology of Pediatric Hydrocephalus and Hydrocephalus-related Diseases

by YAMASAKI, Mami, KANEMURA, Yonehiro
Published 2015

Long term prognosis of fetal hydrocephalus

by Yamada Junji, Yamasaki Mami, Nonaka Masahiro
Published 2005-12-01

Prenatal diagnosis of L1CAM gene mutations in X-linked hydrocephalus

by Yamasaki, Mami, shohuda, Tomoko, Sakamoto, Hiroaki, Nonaka, Masahiro, Kanemura, Yonehiro
Published 2006

Prenatal diagnosis of L1CAM gene mutations in X-linked hydrocephalus

by Kanemura Yonehiro, Nonaka Masahiro, Sakamoto Hiroaki, shohuda Tomoko, Yamasaki Mami
Published 2006-12-01

Evaluation of prenatal diagnosis of isolated ventriculomegaly

by Teramoto Chika, Bamba Yohei, Nonaka Masahiro, Yamasaki Mami, Pooh Rituko
Published 2010-12-01

Feeder-Free Generation and Long-Term Culture of Human Induced Pluripotent Stem Cells Using Pericellular Matrix of Decidua Derived Mesenchymal Cells

by Fukusumi, Hayato, Shofuda, Tomoko, Kanematsu, Daisuke, Yamamoto, Atsuyo, Suemizu, Hiroshi, Nakamura, Masato, Yamasaki, Mami, Ohgushi, Masatoshi, Sasai, Yoshiki, Kanemura, Yonehiro
Published 2013

A case of optic-nerve hypoplasia and anterior segment abnormality associated with facial cleft

by Miyake, Tomoko, Kojima, Shota, Sugiyama, Tetsuya, Ueki, Mari, Sugasawa, Jun, Oku, Hidehiro, Tajiri, Kensuke, Shigemura, Yuka, Ueda, Koichi, Harada, Atsuko, Yamasaki, Mami, Yamanaka, Takumi, Utsunomiya, Hidetsuna, Ikeda, Tsunehiko
Published 2016

Truncating mutation in NFIA causes brain malformation and urinary tract defects

by Negishi, Yutaka, Miya, Fuyuki, Hattori, Ayako, Mizuno, Kentaro, Hori, Ikumi, Ando, Naoki, Okamoto, Nobuhiko, Kato, Mitsuhiro, Tsunoda, Tatsuhiko, Yamasaki, Mami, Kanemura, Yonehiro, Kosaki, Kenjiro, Saitoh, Shinji
Published 2015

A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations

by Miya, Fuyuki, Kato, Mitsuhiro, Shiohama, Tadashi, Okamoto, Nobuhiko, Saitoh, Shinji, Yamasaki, Mami, Shigemizu, Daichi, Abe, Tetsuo, Morizono, Takashi, Boroevich, Keith A., Kosaki, Kenjiro, Kanemura, Yonehiro, Tsunoda, Tatsuhiko
Published 2015

TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis

by Yokoi, Setsuri, Ishihara, Naoko, Miya, Fuyuki, Tsutsumi, Makiko, Yanagihara, Itaru, Fujita, Naoko, Yamamoto, Hiroyuki, Kato, Mitsuhiro, Okamoto, Nobuhiko, Tsunoda, Tatsuhiko, Yamasaki, Mami, Kanemura, Yonehiro, Kosaki, Kenjiro, Kojima, Seiji, Saitoh, Shinji, Kurahashi, Hiroki, Natsume, Jun
Published 2015

In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutations

by Bamba, Yohei, Shofuda, Tomoko, Kato, Mitsuhiro, Pooh, Ritsuko K., Tateishi, Yoko, Takanashi, Jun-ichi, Utsunomiya, Hidetsuna, Sumida, Miho, Kanematsu, Daisuke, Suemizu, Hiroshi, Higuchi, Yuichiro, Akamatsu, Wado, Gallagher, Denis, Miller, Freda D., Yamasaki, Mami, Kanemura, Yonehiro, Okano, Hideyuki
Published 2016