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Brain & Development|August 1, 2007
Inappropriate intracranial hemodynamics in the natural course of MELASJunko Nishioka, Yukihiro Akita, Shuichi Yatsuga, et al.Brain & Development|July 3, 2014
New TRPM6 mutation and management of hypomagnesaemia with secondary hypocalcaemiaKoujyu Katayama, Nataliya Povalko, Shuichi Yatsuga, et al.Journal of Medical Case Reports|August 12, 2016
Developmental delay and failure to thrive in a 7-month-old baby boy with spontaneous transient Graves' thyrotoxicosis: a case reportShuichi Yatsuga, Tomoko Saikusa, Takako Sasaki, et al.Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 5, 2022
Urinary stone in a 12-year-old adolescent with new-onset type 1 diabetes and diabetic ketoacidosisKikumi Ushijima-Fuchino, Yuko Koga, Satoko Umino, et al.Molecular Genetics & Genomic Medicine|May 7, 2019
A case of combined 21-hydroxylase deficiency and CHARGE syndrome featuring micropenis and cryptorchidismSatoko Umino, Miyuki Kitamura, Yuko Katoh-Fukui, et al.Human Genome Variation|May 27, 2017
The first Japanese case of central precocious puberty with a novel <i>MKRN3</i> mutationJunko Nishioka, Hirohito Shima, Maki Fukami, et al.Biochimica Et Biophysica Acta|March 30, 2011
MELAS: a nationwide prospective cohort study of 96 patients in JapanShuichi Yatsuga, Nataliya Povalko, Junko Nishioka, et al.Mitochondrion|December 13, 2005
Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosisIsao Ueki, Yasutoshi Koga, Nataliya Povalko, et al.Clinical Case Reports|January 19, 2019
Temple syndrome diagnosed in an adult patient with clinical autism spectrum disorderTakuro Kimura, Masayo Kagami, Keiko Matsubara, et al.Brain & Development|September 4, 2022
An exploratory study to identify neonatal arterial ischemic stroke: A single-center studyTakashi Setoue, Shuichi Yatsuga, Kazutoshi Ito, et al.Pageof 5