スポンサーリンク
Department of Pediatrics, South Miyagi Medical Center | 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
- Panax Ginseng : A Newly Identified Cause of Gynecomastia
- Human Herpes Virus Type 6 Can Cause Skin Lesions at the BCG Inoculation Site Similar to Kawasaki Disease