Paper

• Acute Myeloid Leukemia in a Patient With X-linked Severe Combined Immunodeficiency.
  Shigemura T, Motobayashi M, Matsuda K, Shimodaira T, Kurata T, Kobayashi N, Agematsu K, Nakazawa Y.
  J Pediatr Hematol Oncol. , 2017
• Early detection of Rhizopus DNA in the serum of a patient with rhino-orbital-cerebral mucormycosis following allogeneic hematopoietic stem cell transplantation.
  Shigemura T, Nishina S, Nakazawa H, Matsuda K, Yaguchi T, Nakazawa Y.
  Int J Hematol., 10(3), 354-5, 2016
• Novel heterozygous C243Y A20/TNFAIP3 gene mutation is responsible for chronic inflammation in autosomal-dominant Behçet's disease.
  Shigemura T, Kaneko N, Kobayashi N, Kobayashi K, Takeuchi Y, Nakano N, Masumoto
  RMD Open., 5(2), 2016
• Gangrenous appendicitis in a patient with severe congenital neutropenia.
  Shigemura T, Ohno Y, Sano K, Uehara T, Terada M, Koike K, Nakazawa Y.
  Pediatr Int., 58(10), 1093-1094, 2016
• Immune Complex-Mediated Glomerulonephritis in a Patient with Wiskott-Aldrich Syndrome.
  Shigemura T, Nakazawa Y, Shimojo H, Kobayashi N, Agematsu K.
  J Clin Immunol., 36(4), 357-9, 2016
• Monitoring serum IL-18 levels is useful for treatment of a patient with systemic juvenile idiopathic arthritis complicated by macrophage activation syndrome.
  Shigemura T, Yamazaki T, Hara Y, Ou JN, Stevens AM, Ochs HD, Koike K, Agematsu K.
  Pediatr Rheumatol J., 13(9), 15, 2011