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Endocrine Journal|August 12, 2006
Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndromeToshihiro Tajima, Mitsuru Nawate, Yutaka Takahashi, et al.Endocrine Journal|December 1, 2012
Clinical and molecular analysis of six Japanese patients with a renal form of pseudohypoaldosteronism type 1Yoriko Hatta, Akie Nakamura, Shinya Hara, et al.The Journal of Clinical Endocrinology and Metabolism|November 5, 2002
Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalaciaYuji Yamazaki, Ryo Okazaki, Minako Shibata, et al.Journal of Bone and Mineral Metabolism|November 2, 2005
Comparison of two assays for fibroblast growth factor (FGF)-23Nobuaki Ito, Seiji Fukumoto, Yasuhiro Takeuchi, et al.The Journal of Clinical Endocrinology and Metabolism|August 25, 2020
Clinical Features of 57 Patients with Lipoid Congenital Adrenal Hyperplasia: Criteria for Nonclassic Form RevisitedTomohiro Ishii, Toshihiro Tajima, Kenichi Kashimada, et al.Clinical Endocrinology|October 1, 2020
The progression of salt-wasting and the body weight change during the first 2 weeks of life in classical 21-hydroxylase deficiency patientsMaki Gau, Kaoru Konishi, Kei Takasawa, et al.International Archives of Allergy and Immunology|April 22, 2015
Low Frequencies of Autoimmunity-Associated PTPN22 Polymorphisms in MODY Patients, Including Those Transiently Expressing Islet Cell AutoantibodiesPetr Heneberg, Milena Malá, Tohru Yorifuji, et al.Clinical and Experimental Nephrology|January 24, 2009
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian familyMohammad Al-Haggar, Ashraf Bakr, Toshihiro Tajima, et al.Diagnostics (Basel, Switzerland)|January 11, 2024
Temporal Trend of the SARS-CoV-2 Omicron Variant and RSV in the Nasal Cavity and Accuracy of the Newly Developed Antigen-Detecting Rapid Diagnostic TestDaisuke Tamura, Yuji Morisawa, Takashi Mato, et al.Clinical Endocrinology|June 11, 2009
Problems in diagnosing atypical Gitelman's syndrome presenting with normomagnesaemiaAkinobu Nakamura, Chikara Shimizu, So Nagai, et al.Pageof 15