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Scientific Reports|December 3, 2024
Perampanel reduces seizure frequency in patients with developmental and epileptic encephalopathy for a long termHirokazu Yamagishi, Hitoshi Osaka, Kazuhiro Muramatsu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 23, 2024
First evaluation of Eyberg Child Behavior Inventory for foster children in JapanMiyuki Matano, Hisayo Katabira, Tomoe Sekine, et al.
Endocrine Journal|March 29, 2026
Congenital aldosterone deficiency and its resistanceToshihiro Tajima, Naoko Amano, Tomohiro Ishii, et al.
The Journal of Clinical Endocrinology and Metabolism|April 13, 2006
Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosteroneKeiko Homma, Tomonobu Hasegawa, Toshiro Nagai, et al.
Endocrine Journal|September 29, 2012
Two novel mutations of the CYP11B2 gene in a Japanese patient with aldosterone deficiency type 1Eisuke Kondo, Akie Nakamura, Keiko Homma, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 1, 2014
Polyarthritis caused by methimazole in two Japanese patients with graves' diseaseHiroko Nihei, Hidenori Tada, Yuki Naruse, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 10, 2023
Guidelines for Newborn Screening of Congenital Hypothyroidism (2021 Revision)Keisuke Nagasaki, Kanshi Minamitani, Akie Nakamura, et al.
Endocrine Journal|October 12, 2016
A novel frameshift mutation in NR3C2 leads to decreased expression of mineralocorticoid receptor: a family with renal pseudohypoaldosteronism type 1Yuki Kawashima Sonoyama, Toshihiro Tajima, Masanobu Fujimoto, et al.
The Journal of Clinical Endocrinology and Metabolism|August 23, 2013
Three novel IGSF1 mutations in four Japanese patients with X-linked congenital central hypothyroidismAkie Nakamura, Beata Bak, Tanya L R Silander, et al.
Endocrine Journal|May 15, 2002
Two novel mutations of thiazide-sensitive Na-Cl cotrans porter (TSC) gene in two sporadic Japanese patients with Gitelman syndromeToshihiro Tajima, Yuichi Kobayashi, Shuji Abe, et al.
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