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Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Two Japanese patients with gitelman syndromeToshihiro Tajima, Yuichi Tabata, Kayoko Tao, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 28, 2006
Molecular genetic analysis of MODY candidate genes in Japanese patients with non-obese juvenile onset diabetes mellitusMasayo Kagami-Takasugi, Noriyuki Katsumata, Toshiaki Tanaka, et al.Pediatric Reports|July 18, 2012
Concurrence of thyrotoxicosis and Gitelman's syndrome-associated hypokalemia-induced periodic paralysisShinsaku Imashuku, Tomoko Teramura-Ikeda, Naoko Kudo, et al.The Journal of Clinical Endocrinology and Metabolism|August 23, 2013
Loss-of-function and gain-of-function mutations of calcium-sensing receptor: functional analysis and the effect of allosteric modulators NPS R-568 and NPS 2143Akie Nakamura, Tomoyuki Hotsubo, Keiji Kobayashi, et al.Nephrology (Carlton, Vic.)|June 29, 2026
Injury to E- and VE-Cadherin in Paediatric Idiopathic Steroid-Sensitive Nephrotic Syndrome: Potential Markers of the Disease StatusTakahiro Kanai, Jun Aoyagi, Masanori Kurosaki, et al.Endocrine Journal|May 1, 2008
Case study of a 15-year-old boy with McCune-Albright syndrome combined with pituitary gigantism: effect of octreotide-long acting release (LAR) and cabergoline therapyToshihiro Tajima, Junko Tsubaki, Katsura Ishizu, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|February 10, 2018
A Japanese patient with congenital central hypothyroidism caused by a novel IGSF1 mutationTakeshi Yamaguchi, Tomoyuki Hothubo, Shuntaro Morikawa, et al.Endocrine Journal|May 29, 2007
A novel missense mutation (P366T) of the LHX4 gene causes severe combined pituitary hormone deficiency with pituitary hypoplasia, ectopic posterior lobe and a poorly developed sella turcicaToshihiro Tajima, Tsukasa Hattori, Takeo Nakajima, et al.The Journal of Urology|May 6, 2004
Expression of vascular endothelial growth factor and its receptors Flk-1 and Flt-1 during the regeneration of autotransplanted adrenal cortex in the adrenalectomized ratAkihisa Taniguchi, Toshihiro Tajima, Katsuya Nonomura, et al.The Journal of Steroid Biochemistry and Molecular Biology|August 29, 2003
Molecular pathogenesis of lipoid adrenal hyperplasia and adrenal hypoplasia congenitaKenji Fujieda, Koji Okuhara, Shuji Abe, et al.Pageof 15