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Journal of Pediatric Gastroenterology and Nutrition|January 6, 2025
Management of pediatric Peutz-Jeghers syndrome: Highlighting the efficacy and safety of endoscopic ischemic polypectomyMika Dofuku, Tomonori Yano, Koji Yokoyama, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|June 26, 2023
A case of papilledema in Camurati-Engelmann disease treated effectively with prednisoloneMaho Asai, Akira Gomi, Nobuhiro Ibaraki, et al.
Endocrine Research|January 26, 2005
P450 oxidoreductase deficiency: a new disorder of steroidogenesis affecting all microsomal P450 enzymesAmit V Pandey, Christa E Flück, Ningwu Huang, et al.
The Journal of Clinical Endocrinology and Metabolism|July 11, 2002
Hydrochlorothiazide effectively reduces urinary calcium excretion in two Japanese patients with gain-of-function mutations of the calcium-sensing receptor geneKohei Sato, Yukihiro Hasegawa, Jun Nakae, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Results from 28 years of newborn screening for congenital adrenal hyperplasia in sapporoShuntaro Morikawa, Akie Nakamura, Kaori Fujikura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 27, 2024
Efficacy of parent-child interaction therapy for children born prematureMiyuki Matano, Koyuru Kurane, Kei Wakabayashi, et al.
Human Genome Variation|May 30, 2025
Partial monosomy 18p and 21q due to a paternal reciprocal translocation leading to holoprosencephalyHiroko Wakabayashi, Ayumi Matsumoto, Sakiko Komori, et al.
The Journal of Clinical Endocrinology and Metabolism|January 10, 2003
Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patientToshihiro Tajima, Tsukasa Hattorri, Takeo Nakajima, et al.
Endocrine Journal|August 11, 2010
Identification and functional analysis of novel calcium-sensing receptor gene mutation in familial hypocalciuric hypercalcemiaKazuhiro Nanjo, So Nagai, Chikara Shimizu, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Central Congenital Hypothyroidism Detected by Neonatal Screening in Sapporo, Japan (2000-2004): It's Prevalence and Clinical CharacteristicsFumie Fujiwara, Kaori Fujikura, Koji Okuhara, et al.
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