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International Journal of Molecular Sciences|December 10, 2021
Bone Biomarkers in MucopolysaccharidosesAkari Nakamura-UtsunomiyaInternational Journal of Molecular Sciences|July 9, 2022
Autoimmunity Related to Adipsic Hypernatremia and ROHHAD SyndromeAkari Nakamura-UtsunomiyaEndocrine Journal|July 7, 2024
Autoimmunity related to anti-Na<sub>x</sub> and anti-ZSCAN1 autoantibodies in adipsic hypernatremiaAkari Nakamura-UtsunomiyaJournal of the Endocrine Society|June 3, 2026
Adherence to daily growth hormone therapy in Japan: real-world data from the Melon Nikki™ app and deviceAkari Nakamura-Utsunomiya, Taisuke Ono, Osamu ArashinInternational Journal of Molecular Sciences|February 10, 2024
Anti-ZSCAN1 Autoantibodies Are a Feasible Diagnostic Marker for ROHHAD Syndrome Not Associated with a TumorAkari Nakamura-Utsunomiya, Kei Yamaguchi, Naoki GoshimaPlos One|April 7, 2020
Downregulation of endothelial nitric oxide synthase (eNOS) and endothelin-1 (ET-1) in a co-culture system with human stimulated X-linked CGD neutrophilsAkari Nakamura-Utsunomiya, Miyuki Tsumura, Satoshi Okada, et al.Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 14, 2017
Characteristic clinical features of adipsic hypernatremia patients with subfornical organ-targeting antibodyAkari Nakamura-Utsunomiya, Takeshi Y Hiyama, Satoshi Okada, et al.CEN Case Reports|August 22, 2021
Analysis of water and electrolyte imbalance in a patient with adipsic hypernatremia associated with subfornical organ-targeting antibodyYoko Shirai, Kenichiro Miura, Akari Nakamura-Utsunomiya, et al.Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 24, 2015
Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of NR3C2Shuntaro Morikawa, Nagisa Komatsu, Sonoko Sakata, et al.Endocrine Journal|August 10, 2021
Current status of transition medicine for 21-hydroxylase deficiency in Japan: from the perspective of pediatric endocrinologistsKei Takasawa, Akari Nakamura-Utsunomiya, Naoko Amano, et al.Pageof 3