A case of pseudohypoparathyroidism type Ia with a novel frameshift mutation in the GNAS gene: early diagnosis of osteoma cutis by skin biopsy

por Kodo, Kazuki, Maeda, Hiroshi, Morimoto, Hidechika, Wada, Makoto, Imura, Tetsuya, Nakajima, Hisakazu
Publicado 2019

Decrement in bone mineral density after parathyroidectomy in a pediatric patient with primary hyperparathyroidism

por Morimoto, Hidechika, Nakajima, Hisakazu, Mori, Jun, Fukuhara, Shota, Shigehara, Keiichi, Adachi, Shinsuke, Hosoi, Hajime
Publicado 2018

Alfacalcidol improves the growth velocity in children with vitamin D deficiency/insufficiency: A single center retrospective cohort study

por Miyagaki, Satoshi, Yamaguchi, Mihoko, Ota, Takeshi, Kawabe, Yasuhiro, Morimoto, Hidechika, Oka, Yoshinobu, Mori, Jun
Publicado 2021

45,X/46,X,psu idic(Y)(q11.2) in a phenotypically normal male with short stature: a case report

por Kawabe, Yasuhiro, Yamaguchi, Mihoko, Miyagaki, Satoshi, Ota, Takeshi, Morimoto, Hidechika, Hattori, Atsushi, Fukami, Maki, Mori, Jun
Publicado 2020

Thyroid hypogenesis is associated with a novel AKT3 germline variant that causes megalencephaly and cortical malformation

por Mori, Jun, Hasegawa, Tatsuji, Miyamoto, Yosuke, Kitamura, Kazumasa, Morimoto, Hidechika, Tozawa, Takenori, Pooh, Ritsuko Kimata, Chiyonobu, Tomohiro
Publicado 2022

Association of Type 2 Deiodinase Thr92Ala Polymorphism with Pediatric Obesity in Japanese Children: A Case-Control Study

por Ota, Takeshi, Mori, Jun, Kawabe, Yasuhiro, Morimoto, Hidechika, Fukuhara, Shota, Kodo, Kazuki, Sugimoto, Satoru, Kosaka, Kitaro, Nakajima, Hisakazu, Hosoi, Hajime
Publicado 2022

High-fat diet accelerates extreme obesity with hyperphagia in female heterozygous Mecp2-null mice

por Fukuhara, Shota, Nakajima, Hisakazu, Sugimoto, Satoru, Kodo, Kazuki, Shigehara, Keiichi, Morimoto, Hidechika, Tsuma, Yusuke, Moroto, Masaharu, Mori, Jun, Kosaka, Kitaro, Morimoto, Masafumi, Hosoi, Hajime
Publicado 2019