S. Takishima

Lower body weight and BMI at birth were associated with early adiposity rebound in 21-hydroxylase deficiency patients.

T. Morio, M. Ono, Y. Hasegawa, 2016, Endocrine journal.

Adrenal suppression and anthropometric data at two years of age was not influenced by the initial hydrocortisone dose in patients with 21-hydroxylase deficiency

T. Morio, Yohei Matsubara, K. Kashimada, 2021, Clinical Pediatric Endocrinology.

Improved growth velocity of a patient with Noonan‐like syndrome with loose anagen hair (NS/LAH) without growth hormone deficiency by low‐dose growth hormone therapy

T. Morio, H. Ohashi, Y. Aoki, 2015, American journal of medical genetics. Part A.

Cause of acute encephalitis/encephalopathy in Japanese children diagnosed by a rapid and comprehensive virological detection system and differences in their clinical presentations

T. Morio, K. Kashimada, Kengo Moriyama, 2018, Brain and Development.

Potential pathological role of single nucleotide polymorphism (c.787T>C) in alkaline phosphatase (ALPL) for the phenotypes of hypophosphatasia.

T. Morio, K. Ozono, T. Kubota, 2020, Endocrine journal.

Pyridoxal 5'-phosphate and related metabolites in hypophosphatasia: Effects of enzyme replacement therapy.

Katsuhiro Kobayashi, T. Akiyama, K. Ozono, 2018, Molecular genetics and metabolism.

Clinical characteristics of adolescent cases with Type A insulin resistance syndrome caused by heterozygous mutations in the β‐subunit of the insulin receptor (INSR) gene

T. Morio, A. Hijikata, T. Shirai, 2018, Journal of diabetes.

Nocturnal enuresis is a possible symptom of pediatric paraganglioma: A case report

K. Kashimada, H. Mochizuki, K. Takasawa, 2020, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.