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British Journal of Haematology|January 6, 2009
Age-associated difference in gene expression of paediatric acute myelomonocytic lineage leukaemia (FAB M4 and M5 subtypes) and its correlation with prognosisAoi Jo, Ichiro Tsukimoto, Eiichi Ishii, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|September 17, 2014
Procalcitonin as a marker of respiratory disorder in neonatesFumihiro Ochi, Takashi Higaki, Masaaki Ohta, et al.
International Journal of Hematology|January 31, 2006
A novel perforin gene mutation in a Japanese family with hemophagocytic lymphohistiocytosisIkuyo Ueda, Urara Kohdera, Shigeyoshi Hibi, et al.
Haematologica|November 21, 2007
Association of transforming growth factor-beta1 gene polymorphism in the development of Epstein-Barr virus-related hematologic diseasesKanako Hatta, Akira Morimoto, Eiichi Ishii, et al.
Clinical Pediatrics|September 29, 2018
Therapeutic Effect of Linezolid in Children With Health Care-Associated Meningitis or VentriculitisFumihiro Ochi, Hisamichi Tauchi, Kozo Nagai, et al.
Haematologica|November 4, 2005
The association of a distinctive allele of NAD(P)H:quinone oxidoreductase with pediatric acute lymphoblastic leukemias with MLL fusion genes in JapanMinenori Eguchi-Ishimae, Mariko Eguchi, Eiichi Ishii, et al.
International Journal of Pediatric Endocrinology|April 24, 2015
Adiponectin/resistin levels and insulin resistance in children: a four country comparison studyKoji Takemoto, Richard J Deckelbaum, Isao Saito, et al.
Case Reports in Transplantation|July 3, 2019
Mesenchymal Stem Cell Therapy Overcomes Steroid Resistance in Severe Gastrointestinal Acute Graft-Versus-Host DiseaseKyoko Moritani, Reiji Miyawaki, Kiriko Tokuda, et al.
Metabolic Brain Disease|September 8, 2017
High mobility group box 1 enhances hyperthermia-induced seizures and secondary epilepsy associated with prolonged hyperthermia-induced seizures in developing ratsMasanori Ito, Hisaaki Takahashi, Hajime Yano, et al.
American Journal of Medical Genetics. Part A|December 22, 2017
Manifestation of recessive combined D-2-, L-2-hydroxyglutaric aciduria in combination with 22q11.2 deletion syndromeMariko Eguchi, Erina Ozaki, Toshifumi Yamauchi, et al.
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