Y. Ogata

Genetic subtypes of familial hemophagocytic lymphohistiocytosis: correlations with clinical features and cytotoxic T lymphocyte/natural killer cell functions.

H. Takada, T. Sasazuki, K. Koike, 2005, Blood.

A Case of Sporadic Blau Syndrome with an Uncommon Clinical Course

Shuichi Yamamoto, M. Imayoshi, Y. Ogata, 2018, Case reports in rheumatology.

Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people

T. Sasazuki, S. Ohga, H. Horiuchi, 2005, Journal of Human Genetics.

High‐dose Cepharanthin for pediatric chronic immune thrombocytopenia in Japan

S. Ohga, A. Ohtake, S. Amemiya, 2017, Pediatrics international : official journal of the Japan Pediatric Society.

Perioperative safety and haematostatic efficacy of a new bypassing agent pd-FVIIa/FX (Byclot) in haemophilia patients with high-responding type inhibitors.

K. Kusuhara, A. Shirahata, A. Ishiguro, 2019, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Nasal hemophilic pseudotumor in a patient with mild hemophilia A and allergic rhinitis

K. Kai, M. Matsuo, M. Monji, 2017, Pediatrics international : official journal of the Japan Pediatric Society.

High frequency of QPY allele and linkage disequilibrium of granzyme-B in Epstein-Barr-virus-associated hemophagocytic lymphohistiocytosis.

H. Wakiguchi, M. Yasukawa, M. Sako, 2004, Tissue antigens.

Partial tandem duplication of MLL gene in acute myeloid leukemia with translocation (11;17)(q23;q12–21)

E. Ishii, N. Sakai, Y. Hamasaki, 2005, American journal of hematology.