Mika Makimura
Kitakyushu, Japan
Last Updated: 09/26/2026
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Found 9 publications
A Decade-Long Diagnostic Challenge: A Case of Nonclassical 21-Hydroxylase Deficiency Mistaken for Polycystic Ovary Syndrome.
Journal: The journal of obstetrics and gynaecology research
Published: August 10, 2025
A case of congenital hyperinsulinism presenting with diabetes after long-term diazoxide therapy.
Journal: Diabetology international
Published: December 20, 2023
Hypocalcemia and Graves' disease associated with 22q11.2 deletion syndrome.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: November 23, 2022
Metabolic and immunological assessment of small-for-gestational-age children during one-year treatment with growth hormone: the clinical impact of apolipoproteins.
Journal: Endocrine journal
Published: February 21, 2018
Placental mesenchymal dysplasia and fetal hematologic disorder.
Journal: Journal of pediatric hematology/oncology
Published: June 27, 2013
N-terminal pro-brain natriuretic peptide as a useful predictor of early surgery in neonates with congenital heart diseases: a prospective observational study.
Journal: Pediatric cardiology
Published: March 25, 2013
Coagulopathy in patients with late-onset ornithine transcarbamylase deficiency in remission state: a previously unrecognized complication.
Journal: Pediatrics
Published: December 05, 2012
Bilateral stenosis of carotid siphon in Hutchinson-Gilford progeria syndrome.
Journal: Brain & development
Published: May 14, 2012
A girl with Hajdu-Cheney syndrome and premature ovarian failure.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: May 11, 2012
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Last Updated: 09/26/2026