KUMAKI Satoru | Department of Pediatrics, South Miyagi Medical Center

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著作論文

A Mutation in the IL-2 Receptor γ Chain Gene Associated with X-linked Severe Combined Immunodeficiency Accompanying Opisthotonus
Omenn Syndrome-Review of Several Phenotypes of Omenn Syndrome and RAG1/RAG2 Mutations in Japan
A novel JAK3 mutation in a Japanese patient with severe combined immunodeficiency
Refractory chronic immune thrombocytopenic purpura in a child with acute lymphoblastic leukemia
Deficient Activity of von Willebrand Factor-Cleaving Protease in Patients With Upshaw-Schulman Syndrome
Prolonged secretion of IL-15 in patients with severe forms of acute graft-versus-host disease after allogeneic bone marrow transplantation in children
Characterization of a Novel Nonsense Mutation in the Interleukin-7 Receptor α Gene in a Korean Patient with Severe Combined Immunodeficiency
Refractory autoimmune hemolytic anemia in a patient with chromosome 22q11.2 deletion syndrome

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