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Allergology International : Official Journal of the Japanese Society of Allergology|July 8, 2017
Flow cytometry-based diagnosis of primary immunodeficiency diseasesHirokazu Kanegane, Akihiro Hoshino, Tsubasa Okano, et al.Journal of Clinical Immunology|November 6, 2016
Hematopoietic Stem Cell Transplantation for XIAP Deficiency in JapanShintaro Ono, Tsubasa Okano, Akihiro Hoshino, et al.Clinical Immunology (Orlando, Fla.)|August 7, 2017
Maternal T and B cell engraftment in two cases of X-linked severe combined immunodeficiency with IgG1 gammopathyTsubasa Okano, Takuro Nishikawa, Eri Watanabe, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|September 6, 2016
Novel compound heterozygous mutations in a Japanese girl with Janus kinase 3 deficiencyTakeshi Sato, Tsubasa Okano, Mari Tanaka-Kubota, et al.Intestinal Research|January 21, 2021
A case of autoimmune enteropathy with CTLA4 haploinsufficiencyHaruka Miyazaki, Namiko Hoshi, Michitaka Kohashi, et al.Pediatric Blood & Cancer|September 30, 2017
Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferationMasatoshi Takagi, Akihiro Hoshino, Kenichi Yoshida, et al.Frontiers in Pediatrics|February 20, 2019
Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG MutationKay Tanita, Akihiro Hoshino, Ken-Ichi Imadome, et al.International Immunology|July 1, 2020
Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutationsSonoko Sakata, Miyuki Tsumura, Tadashi Matsubayashi, et al.Journal of Clinical Immunology|June 8, 2020
Whole-Exome Sequencing-Based Approach for Germline Mutations in Patients with Inborn Errors of ImmunityTsubasa Okano, Kohsuke Imai, Takuya Naruto, et al.The Journal of Infectious Diseases|April 24, 2018
Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 MutationAkihiro Hoshino, Takehiro Takashima, Kenichi Yoshida, et al.Pageof 5