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Endocrinology|September 14, 2024
Circadian Regulatory Networks of Glucose Homeostasis and Its Disruption as a Potential Cause of UndernutritionShinsuke Onuma, Masanobu KawaiClinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 18, 2018
Thyroid hormone status in patients with severe selenium deficiencyMasanobu Kawai, Yasuko Shoji, Shinsuke Onuma, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|June 29, 2020
Growth hormone treatment for extremely low birthweight children born small for gestational ageShinsuke Onuma, Shinobu Ida, Takatoshi Maeyama, et al.Endocrinology|July 29, 2022
The Lack of Bmal1, a Core Clock Gene, in the Intestine Decreases Glucose Absorption in MiceShinsuke Onuma, Saori Kinoshita, Shigeki Shimba, et al.Endocrinology|February 8, 2025
Lack of PTEN in Osteocytes Increases Lipocalin-2 Level and Confers Resistance to High-Fat Diet-Induced Obesity in MiceSaori Kinoshita, Shinsuke Onuma, Natsuko Yamazaki, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|June 11, 2020
Fat distribution in short-stature children born small for gestational ageTakatoshi Maeyama, Shinobu Ida, Shinsuke Onuma, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|August 13, 2021
Urinary iodine and thyroglobulin are useful markers in infants suspected of congenital hypothyroidism based on newborn screeningMakiko Tachibana, Yoko Miyoshi, Miho Fukui, et al.Human Genome Variation|March 21, 2020
MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the <i>SAMD9</i> geneShinsuke Onuma, Tamaki Wada, Ryosuke Araki, et al.Journal of Pediatric Gastroenterology and Nutrition|March 20, 2024
Comprehensive analyses of neurodevelopmental outcomes and quality of life of children with biliary atresiaYoshinori Satomura, Makiko Tachibana, Kie Yasuda, et al.Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|July 21, 2021
Two girls with a neonatal screening-negative 21-hydroxylase deficiency requiring treatment with hydrocortisone for virilization in late childhoodShinsuke Onuma, Tomoya Fukuoka, Yoko Miyoshi, et al.Pageof 2