Sato Y, Haruta M, Kaneko Y, Nakasato Y, Kurosawa H, Yoshihara S. Paternally inherited WT1 mutation plus uniparental disomy of 11p may be an essential mechanism for development of WT1-mutated familial Wilms tumor. Pediatric blood & cancer. 2018. e27442
Hidemitsu Kurosawa, Tomoyuki Mizukami, Hiroyuki Nunoi, Masaya Kato, Yuya Sato, Mayuko Okuya, Keitaro Fukushima, Yoshihiko Katsuyama, Osamu Arisaka. Necrotizing Ulcer after BCG Vaccination in a Girl with Leukocyte-adhesion Deficiency Type 1. Journal of Pediatric Hematology/Oncology. 2018. 40. 1. 63-66
日本小児血液学会
, 日本癌学会
, 日本血液学会
, 日本小児科学会
, The Japanese Society of Pediatric Hematology
, The Japanese Cancer Association
, The Japan Society of Hematology
, Japan Pediatric Society