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Journal of Thyroid Research|November 5, 2010
Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene DefectWakako Jo, Katsura Ishizu, Kenji Fujieda, et al.
Pediatric Research|June 23, 2009
Elevated free thyroxine levels detected by a neonatal screening systemToshihiro Tajima, Wakako Jo, Kaori Fujikura, et al.
The Tohoku Journal of Experimental Medicine|January 26, 2011
A novel PAX4 mutation in a Japanese patient with maturity-onset diabetes of the youngWakako Jo, Machiko Endo, Katura Ishizu, 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.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 31, 2013
Development of endometrial carcinoma in a patient with leprechaunism (donohue syndrome)Wakako Jo, Satoko Sudo, Akie Nakamura, et al.
Endocrine Journal|December 16, 2010
Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndromeAkie Nakamura, Fumie Fujiwara, Yukihiro Hasegawa, et al.
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