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Transfusion|April 28, 2009
Elevated Ca²+ influx-inducing activity toward mast cells in pretransfusion sera from patients who developed transfusion-related adverse reactionsHiroshi Azuma, Miki Yamaguchi, Daisuke Takahashi, et al.
Hearing Research|June 14, 2002
Reduction in the endocochlear potential caused by Cs(+) in the perilymph can be explained by the five-compartment model of the stria vascularisAkinobu Kakigi, Shunji Takeuchi, Motonori Ando, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 12, 2016
High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidismKumihiro Matsuo, Yusuke Tanahashi, Tokuo Mukai, et al.
Journal of Medical Case Reports|June 30, 2022
An infantile case of hereditary folate malabsorption with sudden development of pulmonary hemorrhage: a case reportYukari Sakurai, Naohisa Toriumi, Takeo Sarashina, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 8, 2015
Electroclinical features of epileptic encephalopathy caused by SCN8A mutationSatoru Takahashi, Shiho Yamamoto, Akie Okayama, et al.
Journal of Oncology Pharmacy Practice : Official Publication of the International Society of Oncology Pharmacy Practitioners|August 14, 2020
Breastfeeding in a patient with chronic myeloid leukemia during tyrosine kinase inhibitor therapyRyuta Terao, Mitsumaro Nii, Hiroko Asai, et al.
Pediatric Blood & Cancer|August 19, 2014
A randomized trial of cefozopran versus cefepime as empirical antibiotic treatment of febrile neutropenia in pediatric cancer patientsTakeo Sarashina, Ryoji Kobayashi, Makoto Yoshida, et al.
Pediatric Cardiology|November 13, 2014
Ratio between fms-like tyrosine kinase 1 and placental growth factor in children with congenital heart diseaseMasaya Sugimoto, Hideharu Oka, Aya Kajihama, et al.
BMJ Open|January 22, 2026
Haemoglobin vesicles as artificial red blood cells developed for use as a transfusion alternative: an open-label, single-centre phase Ib study protocol in JapanKazuya Sakai, Kiyoshi Asada, Yudai Watanabe, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|September 13, 2020
A novel STAT3 mutation associated with hyper immunoglobulin E syndrome with a paucity of connective tissue signsYoichiro Yoshida, Tsunehisa Nagamori, Hironori Takahashi, et al.
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