Rituximab Treatment for Nephrotic Syndrome in Children

by Iijima, Kazumoto, Sako, Mayumi, Nozu, Kandai
Published 2014

Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients

by Lee, Tomoko, Takeshima, Yasuhiro, Kusunoki, Noriko, Awano, Hiroyuki, Yagi, Mariko, Matsuo, Masafumi, Iijima, Kazumoto
Published 2014

A Case of Transforming Growth Factor-β-Induced Gene-Related Oculorenal Syndrome: Granular Corneal Dystrophy Type II with a Unique Nephropathy

by Iwafuchi, Yoichi, Morioka, Tetsuo, Oyama, Yuko, Nozu, Kandai, Iijima, Kazumoto, Narita, Ichiei
Published 2016

A 12p13 GRIN2B deletion is associated with developmental delay and macrocephaly

by Morisada, Naoya, Ioroi, Tomoaki, Taniguchi-Ikeda, Mariko, Juan Ye, Ming, Okamoto, Nobuhiko, Yamamoto, Toshiyuki, Iijima, Kazumoto
Published 2016

An unusual case of congenital cytomegalovirus infection-related retinopathy

by Tagami, Mizuki, Honda, Shigeru, Morioka, Ichiro, Iijima, Kazumoto, Yamada, Hideto, Nakamura, Makoto
Published 2016

Yersinia pseudotuberculosis infection in Kawasaki disease and its clinical characteristics

by Horinouchi, Tomoko, Nozu, Kandai, Hamahira, Kiyoshi, Inaguma, Yosuke, Abe, Jun, Nakajima, Hiroshi, Kugo, Masaaki, Iijima, Kazumoto
Published 2015

Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY

by Nozu, Kandai, Iijima, Kazumoto, Ohtsuka, Yasufumi, Fu, Xue Jun, Kaito, Hiroshi, Nakanishi, Koichi, Vorechovsky, Igor
Published 2014

Diverse Renal Phenotypes Observed in a Single Family with a Genetic Mutation in Paired Box Protein 2

by Iwafuchi, Yoichi, Morioka, Tetsuo, Morita, Takashi, Yanagihara, Toshio, Oyama, Yuko, Morisada, Naoya, Iijima, Kazumoto, Narita, Ichiei
Published 2016

Primary pediatric stage III renal diffuse large B-cell lymphoma

by Hayakawa, Akira, Shimotake, Nobuya, Kubokawa, Ikuko, Mitsuda, Yoshihiro, Mori, Takeshi, Yanai, Tomoko, Muramaki, Mototsugu, Miyake, Hideaki, Fujisawa, Masato, Iijima, Kazumoto
Published 2013

Primary pediatric endobronchial Ewing sarcoma family of tumors

by Hayakawa, Akira, Hirase, Satoshi, Matsunoshita, Natsuki, Yamamoto, Nobuyuki, Kubokawa, Ikuko, Mori, Takeshi, Yanai, Tomoko, Maniwa, Yoshimasa, Iijima, Kazumoto
Published 2013

Association of a vascular endothelial growth factor polymorphism with the development of bronchopulmonary dysplasia in Japanese premature newborns

by Fujioka, Kazumichi, Shibata, Akio, Yokota, Tomoyuki, Koda, Tsubasa, Nagasaka, Miwako, Yagi, Mariko, Takeshima, Yasuhiro, Yamada, Hideto, Iijima, Kazumoto, Morioka, Ichiro
Published 2014

Age-specific percentile-based reference curve of serum procalcitonin concentrations in Japanese preterm infants

by Fukuzumi, Noriko, Osawa, Kayo, Sato, Itsuko, Iwatani, Sota, Ishino, Ruri, Hayashi, Nobuhide, Iijima, Kazumoto, Saegusa, Jun, Morioka, Ichiro
Published 2016

A Novel Mutation in a Japanese Family with X-linked Alport Syndrome

by Abe, Yoshifusa, Iyoda, Masayuki, Nozu, Kandai, Hibino, Satoshi, Hihara, Kei, Yamaguchi, Yutaka, Yamamura, Tomohiko, Minamikawa, Shogo, Iijima, Kazumoto, Shibata, Takanori, Itabashi, Kazuo
Published 2016

Transcutaneous bilirubin monitoring predicts unexplained late-onset hemolysis in a very low birthweight infant

by Nagasaka, Miwako, Kikuma, Tomoe, Iwatani, Sota, Kurokawa, Daisuke, Yamana, Keiji, Maeyama, Kaori, Koda, Tsubasa, Matsumoto, Hisayuki, Taniguchi-Ikeda, Mariko, Iijima, Kazumoto, Nakamura, Hajime, Morioka, Ichiro
Published 2016

A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy

by Fu, Xue J, Morisada, Naoya, Hashimoto, Fusako, Taniguchi-Ikeda, Mariko, Hashimura, Yuya, Ohtsubo, Hiromi, Ninchoji, Takeshi, Kaito, Hiroshi, Nozu, Kandai, Takahashi, Eihiko, Nakanishi, Koichi, Kurahashi, Hiroki, Iijima, Kazumoto
Published 2014

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation

by Mishra, Divya, Kato, Takema, Inagaki, Hidehito, Kosho, Tomoki, Wakui, Keiko, Kido, Yasuhiro, Sakazume, Satoru, Taniguchi-Ikeda, Mariko, Morisada, Naoya, Iijima, Kazumoto, Fukushima, Yoshimitsu, Emanuel, Beverly S, Kurahashi, Hiroki
Published 2014

The first report of adolescent TAFRO syndrome, a unique clinicopathologic variant of multicentric Castleman’s disease

by Kubokawa, Ikuko, Yachie, Akihiro, Hayakawa, Akira, Hirase, Satoshi, Yamamoto, Nobuyuki, Mori, Takeshi, Yanai, Tomoko, Takeshima, Yasuhiro, Kyo, Eiryu, Kageyama, Goichi, Nagai, Hiroshi, Uehara, Keiichiro, Kojima, Masaru, Iijima, Kazumoto
Published 2014

Fluorescent protein-based detection of unconjugated bilirubin in newborn serum

by Iwatani, Sota, Nakamura, Hajime, Kurokawa, Daisuke, Yamana, Keiji, Nishida, Kosuke, Fukushima, Sachiyo, Koda, Tsubasa, Nishimura, Noriyuki, Nishio, Hisahide, Iijima, Kazumoto, Miyawaki, Atsushi, Morioka, Ichiro
Published 2016

Gestational age-dependency of height and body mass index trajectories during the first 3 years in Japanese small-for-gestational age children

by Maeyama, Kaori, Morioka, Ichiro, Iwatani, Sota, Fukushima, Sachiyo, Kurokawa, Daisuke, Yamana, Keiji, Nishida, Kosuke, Ohyama, Shohei, Fujioka, Kazumichi, Awano, Hiroyuki, Taniguchi-Ikeda, Mariko, Nozu, Kandai, Nagase, Hiroaki, Nishimura, Noriyuki, Shirai, Chika, Iijima, Kazumoto
Published 2016

Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2

by Yoshimoto, Satomi, Harahap, Nur Imma Fatimah, Hamamura, Yuko, Ar Rochmah, Mawaddah, Shima, Ai, Morisada, Naoya, Shinohara, Masakazu, Saito, Toshio, Saito, Kayoko, Lai, Poh San, Matsuo, Masafumi, Awano, Hiroyuki, Morioka, Ichiro, Iijima, Kazumoto, Nishio, Hisahide
Published 2016