ITOH Masatsune

■FacultyDepartment of Pediatrics
■PositionAssociate Professor

Researcher Profile & Settings

Research

    Overview of research:
    Pediatric endocrinology, Pediatric metabolism, Inborn errors of metabolism

Degree

  • Ph.D in Medicine

Research Activities

Published Papers

  • Tertiary hyperparathyroidism in patients with pseudohypoparathyroidism type 1a, Masatsune Itoh, Michiko Okajima, Yuko Kittaka, Akihiro Yachie, Taizo Wada, Yutaka Saikawa, 　:　, Apr. 2022
  • Three pediatric cases of symptomatic hyponatremia in Prader–Willi syndrome, (Yuji Oto), Nobuyuki Murakami, Ryo Nakagawa, Masatsune Itoh, Toshiro Nagai, Tomoyo Matsubara, Journal of Pediatric Endocrinology and Metabolism, 35:1302-1305, Jul. 2022
  • Utility of 18F-FDG-PET/CT for diagnosis of lung metastasis in a case of adrenal cortical carcinoma, Naoki Okada, Reiko Fijisawa, Masatsune Itoh, Katsuaki Sato, Naoto Watanabe, Nozomu Motono, Miyuki Kono, Yutaka Saikawa, The Japanese Journal of Pediatric Hematology/Oncology, 57:304-308, Jun. 2020
  • Therapeutic relowering serum sodium after overly rapid correction of chronic hyponatremia in a patient with secondary pseudohypoaldosteronism, Mari Morikawa, Chisato Akita, Masatsune Itoh, Yutaka Saikawa, Journal of Japanese Society of Emergency Pediatrics, 19:314-318, Apr. 2020
  • Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions, (Keiko Matsubara), Masatsune Itoh, Kenji Shimizu, Shinji Saito, Keisuke Enomoto, Kazuhiko Nakabayashi, Kenichiro Hata, Kenji Kurosawa, Tsutomu Ogata, Maki Fukami, Masayo Kagami, Clinical Epigenetics, 11:36, Feb. 2019
  • Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis, (Hideo.Sasai), Yuka.Aoyama, Hiroki.Otsuka, Elsayed.Abdelkreem, Yasuhiro.Naiki, Mitsuru.Kubota, Yuji.Sekine, Masatsune.Itoh, Mina.Nakama, Hidenori.Ohnishi, Ryoji.Fujiki, Osamu.Ohara, Toshiyuki.Fukao, Journal of Inherited Metabolic Disease, 40:845-852, Jul. 2017
  • A novel MEN1 mutation in a Japanese adolescent with multiple endocrine neoplasia type 1, Masatsune.Itoh, Yutaka.Saikawa, Clinical pediatric endocrinology, 26:25-28, Jan. 2017
  • A novel frameshift mutation in the TRPS1 gene caused Tricho-rhino-phalangeal syndrome type I and III in a Japanese family, M.Itoh, Y.Kittaka, Y.Niida, Y.Saikawa, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 25:115-118, 2016
  • Angelman Syndrome Caused by Chromosomal Rearrangements: A Case Report of 46,XX,+der(13)t(13;15)(q14.1;q12)mat,-15 with an Atypical Phenotype and Review of the Literature, Y.Niida, H.Sato, M.Ozaki, M.Itoh, K.Ikeno, E.Takase, Cytogenetic and genome research, 149:247-257, 2016
  • Determination a relevant period of the preventive gonadal resection in Y-chromosome-related disorders of sex development(DSD)., T.Kuwahara, M.Kohno, S.Takahashi, Y.Yasui, T.Oshikiri, M.Ito, Y.Saikawa, 49:969-974, Aug. 2013
  • Two cases of 22q11.2 deletion syndrome with anorectal anomalies and growth retardation, (K.Nagasaki), M.Ito, O.Naoki, M.Kubota, T.Kikuchi, M.Uchiyama, Journal of pediatric endocrinology & metabolism : JPEM, 24:585-586, 2011
  • Analyses of New Outpatients who had a Chief Complaint of Short Stature in a Single Institution and the Significance of Medical Screening for Short Stature, 36:6-9, Oct. 2009
  • Functional studies of a duplication mutation of valine at 235 by a transient expression assay in a boy with MCT8 deficiency, M.Ito, 32:156-161, Oct. 2007
  • An inherited disorder characterized by repeated episodes of bilateral ballism: a case report, H.Kakinuma, A.Hori, M.Ito, T.Nakamura, H.Takahashi, Movement disorders : official journal of the Movement Disorder Society., 22:2110-2131, Sep. 2007
  • Clinial importance of basic life support in childhood submersion, Y.Matsue, T.Nakamura, H.Sato, C.Akita, M.Hiramatsu, T.Kito, C.Kitaoka, J.Yamamura, T.Ikeda, T.Fujiki, M.Ito, A.Kobayashi, T.Nakamura, H.Kakinuma, E.Koh, H.Takahashi, 60:1195-1199, Jun. 2007
  • Insulin responses to selective arterial calcium infusion under hyperinsulinemic euglycemic glucose clamps: case studies in adult nesidioblastosis and childhood insulinoma, A.Nakagawa, K.Ueno, M.Ito, S.Okamoto, K.Uehara, H.Ito, S.Mishina, E.Kinoshita, T.Nojima, H.Takahashi, H.Ikawa, S.Takashima, M.Nishizawa, S.Nakano, T.Kigoshi, H.Nakabayashi, K.Uchida, Endocrine journal., 54:27-33, 2007
  • Attenuation of gadolinium enhancement in pituitary gland on magnetic resonance imaging of patients with pediatric growth hormone deficiency, (Mariko Doai), Yuka Nishino, Yasuhiko Hayashi, Masatsune Ito, Munetaka Matoba., BMC medical imaging., 17:188, Nov. 2023
  • Criteria for Initiation of CH Treatment, (Keisuke Nagasaki), Kanshi Minamitani, Akie Nakamura, Hironori Kobatashi,Chikahiko Numakura, Masatsune Itoh, Yuichi Mushimoto, Kaori Fujikura,Masaru Fukushi, Toshihiro Tajima, Clinical Pediatric Endocrinology, 32:33, Jan. 2023

Books etc

  • Criteria for Initiation of CH Treatment
    Clinical Pediatric Endocrinology
    (Keisuke Nagasaki), Kanshi Minamitani, Akie Nakamura, Hironori Kobatashi, Chikahiko Numakura, Masatsune Itoh, Yuichi Mushimoto, Kaori Fujikura, Masaru Fukushi, Toshihiro Tajima
      Jan. 2023
  • Reevaluation of Thyroid Function for Differentiation of Transient and Permanent CH and Disease Type Diagnosis
    Clinical Pediatric Endocrinology
    (Keisuke Nagasaki), Kanshi Minamitani, Akie Nakamura, Hironori Kobatashi, Chikahiko Numakura, Masatsune Itoh, Yuichi Mushimoto, Kaori Fujikura, Masaru Fukushi, Toshihiro Tajima
      Jan. 2023