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Cancer Science|April 13, 2013
Characterization of genetic lesions in rhabdomyosarcoma using a high-density single nucleotide polymorphism arrayRiki Nishimura, Junko Takita, Aiko Sato-Otsubo, et al.
Journal of Pediatric Hematology/Oncology|June 24, 2006
Congenital neuroblastoma in a patient with partial trisomy of 2pYuri Dowa, Toshiyuki Yamamoto, Yasuko Abe, et al.
Human Pathology|July 15, 2017
Inflammatory myofibroblastic tumors of the lung carrying a chimeric A2M-ALK gene: report of 2 infantile cases and review of the differential diagnosis of infantile pulmonary lesionsMio Tanaka, Kenichi Kohashi, Kei Kushitani, et al.
Journal of Pediatric Surgery|April 19, 2011
Papillary carcinoma with extensive squamous metaplasia arising from thyroglossal duct cyst in an 11-year-old girl: significance of differentiation from squamous cell carcinoma: a case reportKiyoshi Gomi, Norihiko Kitagawa, Yoshiko Usui, et al.
Plos One|November 8, 2018
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiencyHirohito Shima, Mie Hayashi, Takashi Tachibana, et al.
Journal of Pediatric Hematology/Oncology|June 1, 2017
The Collagen Gel Droplet-embedded Culture Drug Sensitivity Test in Relapsed HepatoblastomaHiroaki Goto, Norihiko Kitagawa, Hironobu Sekiguchi, et al.
International Journal of Hematology|March 24, 2026
Acute megakaryoblastic leukemia with RBM15::MKL1 fusion presenting as neonatal acute liver failure: rescued by living-donor liver transplantationHiroki Yoshinari, Yuta Kawahara, Hitomi Niijima, et al.
Journal of Pediatric Hematology/Oncology|May 1, 2024
Metronomic Chemotherapy for Pediatric Refractory Solid Tumors: A Retrospective Single-center StudyYukari Sakurai, Fuminori Iwasaki, Ayana Hirose, et al.
Frontiers in Oncology|December 7, 2020
A MicroRNA Cluster in the DLK1-DIO3 Imprinted Region on Chromosome 14q32.2 Is Dysregulated in Metastatic HepatoblastomasShohei Honda, Aniruddha Chatterjee, Anna L Leichter, et al.
Pediatric Surgery International|August 25, 2009
Outcome of pediatric renal tumor treated using the Japan Wilms Tumor Study-1 (JWiTS-1) protocol: a report from the JWiTS groupTakaharu Oue, Masahiro Fukuzawa, Hajime Okita, et al.
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