Asymptomatic Congenital Hyperinsulinism due to a Glucokinase-Activating Mutation, Treated as Adrenal Insufficiency for Twelve Years

por Morishita, Kae, Kyo, Chika, Yonemoto, Takako, Kosugi, Rieko, Ogawa, Tatsuo, Inoue, Tatsuhide
Publicado 2017

An Asymptomatic Case With MEN1 Slipping Through Genetic Screening by SNV-dependent Allelic Dropout

por Kosugi, Rieko, Ariyasu, Hiroyuki, Kyo, Chika, Yonemoto, Takako, Ogawa, Tatsuo, Kotani, Masato, Saito, Kohei, Inoue, Tatsuhide, Usui, Takeshi
Publicado 2022

SAT-232 Pheochromocytoma Presenting Rare Skin Findings: Livedoid Vasculopathy and Raynaud’s Phenomenon

por Kyo, Chika, Usui, Takeshi, Yamada, Kanako, Torii-Hanakita, Mizuki, Kosugi, Rieko, Yonemoto, Takako, Ogawa, Tatuo, Kotani, Masato, Tamura, Naohisa, Inoue, Tatsuhide
Publicado 2020

Comparisons of plasma aldosterone and renin data between an automated chemiluminescent immunoanalyzer and conventional radioimmunoassays in the screening and diagnosis of primary a...

por Tamura, Naohisa, Watanabe, Erika, Shirakawa, Rumi, Nakatani, Eiji, Yamada, Kanako, Hatakeyama, Hiroshi, Torii-Hanakita, Mizuki, Kyo, Chika, Kosugi, Rieko, Ogawa, Tatsuo, Kotani, Masato, Usui, Takeshi, Inoue, Tatsuhide
Publicado 2021

ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers

por Kyo, Chika, Usui, Takeshi, Kosugi, Rieko, Torii, Mizuki, Yonemoto, Takako, Ogawa, Tatsuo, Kotani, Masato, Tamura, Naohisa, Yamamoto, Yutaro, Katabami, Takuyuki, Kurihara, Isao, Saito, Kohei, Kanamoto, Naotetsu, Fukuoka, Hidenori, Wada, Norio, Murabe, Hiroyuki, Inoue, Tatsuhide
Publicado 2019