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BMJ Open|April 9, 2016
Impact of the great east Japan earthquake on the body mass index of preschool children: a nationwide nursery school surveyHiroshi Yokomichi, Wei Zheng, Hiroko Matsubara, et al.
Journal of Korean Medical Science|July 2, 2015
Disease-specific Growth Charts of Marfan Syndrome Patients in KoreaYounghee Kwun, Su Jin Kim, Jieun Lee, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 8, 2021
Dmp1Cre-directed knockdown of parathyroid hormone-related protein (PTHrP) in murine decidua is associated with a life-long increase in bone mass, width, and strength in male progenyNiloufar Ansari, Tsuyoshi Isojima, Blessing Crimeen-Irwin, et al.
European Journal of Human Genetics : EJHG|May 28, 2020
Clinical and genetic characterization of nephropathy in patients with nail-patella syndromeYutaka Harita, Seiya Urae, Riki Akashio, et al.
BMJ Global Health|June 8, 2017
Disease prevalence among nursery school children after the Great East Japan earthquakeMami Ishikuro, Hiroko Matsubara, Masahiro Kikuya, et al.
Journal of Epidemiology|June 4, 2017
Alterations in physique among young children after the Great East Japan Earthquake: Results from a nationwide surveyMasahiro Kikuya, Hiroko Matsubara, Mami Ishikuro, et al.
Journal of Diabetes Investigation|March 22, 2019
Pregnancy outcome of Japanese patients with glucokinase-maturity-onset diabetes of the youngYuki Hosokawa, Shinji Higuchi, Rie Kawakita, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 29, 2019
Nonosmotic secretion of arginine vasopressin and salt loss in hyponatremia in Kawasaki diseaseKenichiro Miura, Yutaka Harita, Naoto Takahashi, et al.
Genetics in Medicine Open|December 13, 2024
Loss of function in NSD2 causes DNA methylation signature similar to that in Wolf-Hirschhorn syndromeTomoko Kawai, Shiori Kinoshita, Yuka Takayama, et al.
The Journal of Clinical Endocrinology and Metabolism|February 19, 2024
Genotype-Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG DefectsKanako Tanase-Nakao, Megumi Iwahashi-Odano, Chiho Sugisawa, et al.
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