
I am a Japanese pediatrician with strong background both of clinical practice and scientific research. I experienced a lot in practice fields including general pediatrics, neonatal unit, and endocrinology. I have been taking care of numerous patients with from common diseases to chronic rare displeases. Along to the clinical career, I have piled up scientific careers in lab publishing achievements in both of scientific journal or domestic or international conferences.
I speak and write excellent English in both of daily conversations and scientific occasion. I have written numbers of scientific articles in English published in peer-reviewed journals. I had several chances to speech in the international conferences. I had invited talk in Research Unit in CHUV and UNIL, Lausanne Switzerland. I worked in Nestle Institute of Health Science in Lausanne Switzerland, in which I achieved smooth communication with all the colleagues and bosses in English. I will take OET soon, to obtain the grade B.
Original articles (Peer-reviewed)
S Abali, M Tamura, A Bereket. Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route. J Pediatric Endocrinology and Metabolism. 28; 33 (4): 557-562 (2020).
Y Oda, M Tamura, S Kitanaka. A 12-year-old girl with familial dysalbuminemic hyperthyroxinemia. Pediatrics International. 61(5):520-522,2019 (2019).
M Tamura, M Ishizawa, T Isojima, S Özen, A Oka, M Makishima, S Kitanaka. Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia. Scientific Reports. 7: 5102. (2017).
M Itoh, J Tomio, S Toyokawa, M Tamura, T Isojima, S Kitanaka, Y Kobayashi. Vitamin D-Deficient Rickets in Japan. Global Pediatric Health. 4; 1-5. (2017).
M Tamura, T Isojima, T Kasama, R Mafune, K Shimoda, H Yasudo, H Tanaka, C Takahashi, A Oka, S Kitanaka. Novel DHCR7 mutation in a case of Smith-Lemli-Opitz syndrome, showing 46,XY disorder of sex development. Human Genome Variation. 4, 17015. (2017).
M Tamura, T Isojima, M Kawashima, H Yoshida, K Yamamoto, T Kitaoka, N Namba, A Oka, K Ozono, K Tokunaga, S Kitanaka. Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array. PLoS One Jul 8;10(7): e0131157 (2015).
T Isojima, M Ishizawa, K Yoshimura, M Tamura, S Hirose, M Makishima, S Kitanaka. Hereditary 1,25-Dihydroxyvitamin D-resistant rickets (HVDRR) caused by a VDR mutation: a novel mechanism of dominant inheritance. Bone Reports 2:68-73 (2015).
M Tsuchihashi (maiden name), S Nano, W Fuji, Y Kasamatsu, R Nakao, K Yokoyama. (A pulmonary cancer case presenting resistance for chemotherapy.) Shojinkai Igakushi (1):63-4 (2010).
T Yoshida, M Horinaka, M Takara, M Tsuchihashi (maiden name), N Mukai, M Wakada, T Sakai. Combination of isoliquiritigenin and tumor necrosis factor-related apoptosis-inducing ligand induces apoptosis in colon cancer HT29 cells. Environmental Health and Preventive Medicine 13: 281-7 (2008).
Book Chapters
M Tamura. Cortisol, in 小児臨床検査ガイド (Pediatric Clinical Examination Guide). M Mizuguchi, A Oka, K Onai, Editor. 2017. Bunko-do. p. 282-285.
90.1. M Tamura. DHEA-S, in 小児臨床検査ガイド (Pediatric Clinical Examination Guide). M Mizuguchi, A Oka, K Onai, Editor. 2017. Bunko-do. p. 286-290.
M Tamura. Molecular cell biology study for hereditary dihydroxyvitamin D resistant rickets and anti-diabetic drug based on AMPK. DOHaD Research Unit in CHUV and UNIL. Lausanne, May, 2019.
M Tamura, T Isojima, S Kitanaka. (An HVDRR case caused by uniparental disomy of chromosome 12 : Utility of SNP array.) Spring Seminar of Pediatric Endocrinology 2014. Osaka, June 2014.
2016/04-2018/03 Research Fellowship for Young Scientists, Japan Society for the Promotion of Science, JSPS
2016/12 Research Encouragement Prize, Department of Pediatrics Alumni Association, The University of Tokyo School of Medicine
2016/02 Best Presentation Awards, the 35th Study Group Working on Pediatric Growth
2013/10 Best Presentation Awards, The 47th Annual Scientific Meeting of the Japanese Society for Pediatric Endocrinology
2013/09 ESPE 9th Joint Meeting Travel Awards; Nordiscience Awards, Japanese Society for Pediatric Endocrinology, Novo Nordisk Pharma
Available on request
The Japan Pediatric Society
The Japanese Society of Pediatric Endocrinology
The Japan Endocrine Society