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Hokkaido University Collection of Scholarly and Academic Papers >
Showing results 1 to 5 of 5
Type | Author(s) | Title | Other Titles | Citation | Citation(alt) | Issue Date | article | Namatame-Ohta, Noriko; Morikawa, Shuntaro; Nakamura, Akie; Matsuo, Kumihiro; Nakajima, Masahide; Tomizawa, Kazuhiro; Tanahashi, Yusuke; Tajima, Toshihiro | Four Japanese Patients with Congenital Nephrogenic Diabetes Insipidus due to the AVPR2 Mutations | - | Case reports in pediatrics | - | 3-Jul-2018 |
article | Nanjo, Kazuhiro; Nagai, So; Shimizu, Chikara; Tajima, Toshihiro; Kondo, Takuma; Miyoshi, Hideaki; Yoshioka, Narihito; Koike, Takao | Identification and functional analysis of novel calcium-sensing receptor gene mutation in familial hypocalciuric hypercalcemia | - | Endocrine journal | - | Sep-2010 |
article | Nakamura, Akie; Hotsubo, Tomoyuki; Kobayashi, Keiji; Mochizuki, Hiroshi; Ishizu, Katsura; Tajima, Toshihiro | 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 2143 | - | Journal of clinical endocrinology & metabolism | - | Oct-2013 |
article (author version) | Morikawa, Shuntaro; Tajima, Toshihiro; Nakamura, Akie; Ishizu, Katsura; Ariga, Tadashi | A novel heterozygous mutation of the WFS1 gene leading to constitutive endoplasmic reticulum stress is the cause of Wolfram syndrome | Constitutive ER stress and Wolfram syndrome | Pediatric diabetes | - | Dec-2017 |
article | Nakamura, Akie; Bak, Beata; Silander, Tanya L. R.; Lam, Jessica; Hotsubo, Tomoyuki; Yorifuji, Toru; Ishizu, Katsura; Bernard, Daniel J.; Tajima, Toshihiro | Three Novel IGSF1 Mutations in Four Japanese Patients With X-Linked Congenital Central Hypothyroidism | - | Journal of clinical endocrinology & metabolism | - | Oct-2013 |
Showing results 1 to 5 of 5
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