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Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 19, 2021
Investigation of TSH receptor blocking antibodies in childhood-onset atrophic autoimmune thyroiditisKeisuke Nagasaki, Akie Nakamura, Takeru Yamauchi, et al.
Pediatric Diabetes|November 9, 2011
Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitusTohru Yorifuji, Rika Fujimaru, Yuki Hosokawa, et al.
Cells|December 24, 2025
Altered Sphingolipids, Glycerophospholipids, and Lysophospholipids Reflect Disease Status in Idiopathic Steroid-Sensitive Nephrotic Syndrome in Children: A Non-Targeted Metabolomic StudyTakahiro Kanai, Hideo Ogiso, Jun Aoyagi, et al.
Endocrine Journal|April 24, 2020
Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in JapanShuichi Yatsuga, Naoko Amano, Akari Nakamura-Utsunomiya, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 24, 2015
Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision), , , et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 14, 2017
Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in JapanKeisuke Nagasaki, Takuo Kubota, Hironori Kobayashi, et al.
Hormone Research in Paediatrics|February 19, 2018
Incidence and Characteristics of Adrenal Crisis in Children Younger than 7 Years with 21-Hydroxylase Deficiency: A Nationwide Survey in JapanTomohiro Ishii, Masanori Adachi, Kei Takasawa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Temple syndrome: comprehensive molecular and clinical findings in 32 Japanese patientsMasayo Kagami, Keisuke Nagasaki, Rika Kosaki, et al.
The Journal of Clinical Endocrinology and Metabolism|June 3, 2016
Complex Genomic Rearrangement Within the GNAS Region Associated With Familial Pseudohypoparathyroidism Type 1bAkie Nakamura, Erika Hamaguchi, Reiko Horikawa, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 24, 2015
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision), , , et al.
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