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Pediatrics and Neonatology|May 28, 2014
Severe Hemolytic Jaundice in a Neonate with a Novel COL4A1 MutationSeiichi Tomotaki, Hiroshi Mizumoto, Takayuki Hamabata, et al.Pediatric Hematology and Oncology|January 29, 2011
Depressed levels of interferon-gamma and HLA-DR+CD3+ T cells in infants with transient hyperferritinemiaMitsutaka Shiota, Akira Kumakura, Hiroshi Mizumoto, et al.Human Vaccines & Immunotherapeutics|May 29, 2012
Low response to a monovalent inactivated unadjuvanted influenza A (H1N1) pdm09 vaccine in pediatricians of a general hospital in JapanAtsuko Hata, Chihiro Mano, Yoshie Nakamura, et al.Journal of Pediatric Hematology/Oncology|February 6, 2009
Hereditary spherocytosis in 3 children coexisting with UDP-glucuronyl transferase 1A1 deficiencyMitsutaka Shiota, Junko Asada, Hitoshi Nishida, et al.JACC. Clinical Electrophysiology|May 17, 2018
Comorbid Epilepsy and Developmental Disorders in Congenital Long QT Syndrome With Life-Threatening Perinatal ArrhythmiasAya Miyazaki, Heima Sakaguchi, Takeshi Aiba, et al.European Journal of Pediatrics|January 18, 2006
Familial hemophagocytic lymphohistiocytosis with the MUNC13-4 mutation: a case reportHiroshi Mizumoto, Daisuke Hata, Ken Yamamoto, et al.Neurology|March 29, 2013
ADORA2A polymorphism predisposes children to encephalopathy with febrile status epilepticusMayu Shinohara, Makiko Saitoh, Daisuke Nishizawa, et al.Brain & Development|July 29, 2019
Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathyAkiko Shibata, Mariko Kasai, Ai Hoshino, et al.Annals of Neurology|December 11, 2012
Phenotypic spectrum of COL4A1 mutations: porencephaly to schizencephalyYuriko Yoneda, Kazuhiro Haginoya, Mitsuhiro Kato, et al.Pageof 2