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BMC Research Notes|March 13, 2014
Human parvovirus B19-induced aplastic crisis in an adult patient with hereditary spherocytosis: a case report and review of the literatureYujin Kobayashi, Yoshihiro Hatta, Yusaku Ishiwatari, et al.American Journal of Medical Genetics. Part A|December 11, 2019
Primrose syndrome associated with unclassified immunodeficiency and a novel ZBTB20 mutationKeiko Yamamoto-Shimojima, Taichi Imaizumi, Hiroyuki Akagawa, et al.Experimental Hematology|July 31, 2007
Glycolytic inhibition by mutation of pyruvate kinase gene increases oxidative stress and causes apoptosis of a pyruvate kinase deficient cell lineKen-ichi Aisaki, Shin Aizawa, Hisaichi Fujii, et al.Journal of Nippon Medical School = Nippon Ika Daigaku Zasshi|February 4, 2020
Postoperative Infection after Colorectal Surgery: Subanalysis of Data from the 2015 Japan Postoperative Infectious Complications SurveyHiroshi Maruyama, Shinya Kusachi, Hiroshi Makino, et al.Digestive Surgery|July 30, 2010
Vagotomy suppresses body weight gain in a rat model of gastric bandingHitoshi Kanno, Teruo Kiyama, Itsuo Fujita, et al.Journal of Nippon Medical School = Nippon Ika Daigaku Zasshi|September 11, 2008
Rat gastric banding model for bariatric surgeryHitoshi Kanno, Teruo Kiyama, Itsuo Fujita, et al.Oncology Reports|July 14, 2005
Cyclic polylactate inhibited growth of cloned leukemic cells through reducing glycolytic enzyme activitiesTomonori Harada, Masaya Nagasu, Isao Tsuboi, et al.Journal of Nippon Medical School = Nippon Ika Daigaku Zasshi|September 17, 2009
A case of metastatic hemangiopericytoma occurring 16 years after initial presentation: with special reference to the clinical behavior and treatment of metastatic hemangiopericytomaItsuo Fujita, Teruo Kiyama, Kazumitsu Chou, et al.Internal Medicine (Tokyo, Japan)|June 1, 2022
A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's SyndromeYuma Nato, Yuki Kageyama, Kazutaka Suzuki, et al.Journal of Human Genetics|August 9, 2024
Reciprocal chromosome translocation t(3;4)(q27;q31.2) with deletion of 3q27 and reduced FBXW7 expression in a patient with developmental delay, hypotonia, and seizuresTakeaki Tamura, Keiko Shimojima Yamamoto, Jun Tohyama, et al.Pageof 10