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  • 23 Similar Profiles
Hemophagocytic Lymphohistiocytosis Medicine & Life Sciences
Human Herpesvirus 4 Medicine & Life Sciences
Epstein-Barr Virus Infections Medicine & Life Sciences
Japan Medicine & Life Sciences
Mutation Medicine & Life Sciences
T-Lymphocytes Medicine & Life Sciences
Aplastic Anemia Medicine & Life Sciences
Therapeutics Medicine & Life Sciences

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Research Output 1987 2019

An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome

Okuzono, S., Fukai, R., Noda, M., Miyake, N., Lee, S., Kaku, N., Sanefuji, M., Akamine, S., Kanno, S., Ishizaki, Y., Torisu, H., Kira, R., Matsumoto, N., Sakai, Y. & Ohga, S., Apr 1 2019, In : Brain and Development. 41, 4, p. 378-381 4 p.

Research output: Contribution to journalArticle

Brain Diseases
Inborn Genetic Diseases
Sick Leave

A nationwide survey on tracheostomy for very-low-birth-weight infants in Japan

on behalf of the Neonatal Research Network of Japan, Jan 1 2019, In : Pediatric Pulmonology. 54, 1, p. 53-60 8 p.

Research output: Contribution to journalArticle

Very Low Birth Weight Infant
Odds Ratio

Correction to: Factors predicting the recurrence of Epstein–Barr virus-associated hemophagocytic lymphohistiocytosis in children after treatment using the HLH-2004 protocol (International Journal of Hematology, (2019), 109, 5, (612-617), 10.1007/s12185-019-02612-2)

Yanagisawa, R., Matsuda, K., Ohga, S., Kanegane, H., Morimoto, A., Okamoto, Y., Ohara, A., Fukushima, K., Sotomatsu, M., Nomura, K., Saito, A. M., Horibe, K., Ishii, E. & Nakazawa, Y., May 3 2019, In : International journal of hematology. 109, 5, 1 p.

Research output: Contribution to journalComment/debate

Open Access
Hemophagocytic Lymphohistiocytosis

Diagnostic challenge of the newborn patients with heritable protein C deficiency

Ichiyama, M., Inoue, H., Ochiai, M., ishimura, M., Shiraishi, A., Fujiyoshi, J., Yamashita, H., Sato, K., Matsumoto, S., Hotta, T., Uchiumi, T., Kang, D. & Ohga, S., Feb 1 2019, In : Journal of Perinatology. 39, 2, p. 212-219 8 p.

Research output: Contribution to journalArticle

Protein C Deficiency
Protein C
Protein S
Newborn Infant

Early canakinumab therapy for the sensorineural deafness in a family with Muckle-Wells syndrome due to a novel mutation of NLRP3 gene

Iida, Y., Wakiguchi, H., Okazaki, F., Nakamura, T., Yasudo, H., Kubo, M., Sugahara, K., Yamashita, H., Suehiro, Y., Okayama, N., Hashimoto, K., Iwamoto, N., Kawakami, A., Aoki, Y., Takada, H., Ohga, S. & Hasegawa, S., Mar 14 2019, In : Clinical Rheumatology. 38, 3, p. 943-948 6 p.

Research output: Contribution to journalArticle

Cryopyrin-Associated Periodic Syndromes
Secondary Prevention