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Autoimmune thyroid disease following hematopoietic stem cell transplantation in childhood cancer survivors
Shunsuke Shimazaki, Itsuro Kazukawa, Masanori Minagawa
Clin Pediatr Endocrinol. 2022; 31(2): 54–58.
Various phenotypes of short stature with heterozygous IGF-1 receptor (IGF1R) mutations
Yuki Kawashima-Sonoyama, Tomoyuki Hotsubo, Takashi Hamajima, Naoki Hamajima, Masanobu Fujimoto, Noriyuki Namba, Susumu Kanzaki
Clin Pediatr Endocrinol. 2022; 31(2): 59–67.
Hyperandrogenism correlates with psychological symptoms in adolescents with polycystic ovary syndrome
Zeynep Donbaloğlu, Hale Tuhan, Özge Gizli Çoban, Deniz Özalp Kızılay, Eren İsmailoğlu, Arif Önder, Sezer Acar, Aynur Bedel, Ebru Barsal Çetiner, Berna Singin, Harun Erdem, Mesut Parlak
Clin Pediatr Endocrinol. 2022; 31(2): 68–76.
Transient hypercalcemia followed by hypocalcemia in a preterm infant after maternal magnesium sulfate therapy
Takahiro Tominaga, Kazushige Ikeda, Midori Awazu
Clin Pediatr Endocrinol. 2022; 31(2): 77–80.
Severe hypernatremia in soft drink ketoacidosis and hyperglycemic hyperosmolar state at the onset of type 2 diabetes mellitus: a case series of three adolescents
Soo Jeong Choo, Hyun Gyung Lee, Chan Jong Kim, Eun Mi Yang
Clin Pediatr Endocrinol. 2022; 31(2): 81–86.
Oral disintegrating desmopressin tablet is effective for partial congenital nephrogenic diabetes insipidus with AVPR2 mutation: a case report
Kento Ikegawa, Rumi Hachiya, Kazuhisa Akiba, Yukihiro Hasegawa
Clin Pediatr Endocrinol. 2022; 31(2): 87–92.
High-dose fludrocortisone therapy was transiently required in a female neonate with 21-hydroxylase deficiency
Yusuke Kawasaki, Takeshi Sato, Satsuki Nakano, Takeshi Usui, Satoshi Narumi, Tomohiro Ishii, Tomonobu Hasegawa
Clin Pediatr Endocrinol. 2022; 31(2): 93–97.
A novel nonsense variant (p.Arg1293Ter) of the immunoglobulin superfamily 1 (IGSF1) associated with congenital hypogonadotropic hypogonadism and central hypothyroidism
Toshihiro Tajima, Makiko Oguma
Clin Pediatr Endocrinol. 2022; 31(2): 98–100.