Yamaguchi H, Nagase H, Nishiyama M, Tokumoto S, Ishida Y, Tomioka K, Tanaka T, Fujita K, Toyoshima D, Nishimura N, Kurosawa H, Nozu K, Maruyama A, Tanaka R, Iijima K. Nonconvulsive Seizure Detection by Reduced-Lead Electroencephalography in Children with Altered Mental Status in the Emergency Department. The Journal of pediatrics. 2019. 207. 213-219.e3
Hashikami K, Asahina M, Nozu K, Iijima K, Nagata M, Takeyama M. Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation. Biochemistry and biophysics reports. 2019. 17. 81-86
Nishiyama M, Nagase H, Tomioka K, Tanaka T, Yamaguchi H, Ishida Y, Toyoshima D, Fujita K, Maruyama A, Sasaki K, Oyazato Y, Nakagawa T, Takami Y, Nozu K, Nishimura N, Nakashima I, Iijima K. Clinical time course of pediatric acute disseminated encephalomyelitis. Brain & development. 2019
Lee JM, Nozu K, Choi DE, Kang HG, Ha IS, Cheong HI. Features of Autosomal Recessive Alport Syndrome: A Systematic Review. Journal of clinical medicine. 2019. 8. 2
Sakakibara N, Morisada N, Nozu K, Nagatani K, Ohta T, Shimizu J, Wada T, Shima Y, Yamamura T, Minamikawa S, Fujimura J, Horinouchi T, Nagano C, Shono A, Ye MJ, Nozu Y, Nakanishi K, Iijima K. Clinical spectrum of male patients with OFD1 mutations. Journal of human genetics. 2019. 64. 1. 3-9
