If you made any changes in Pure these will be visible here soon.

Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 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

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

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
Exome
Mutation
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
Tracheostomy
Japan
Odds Ratio
Parturition

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
Hematology
Names
Publications
Viruses

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
Mutation

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
Deafness
Secondary Prevention
Mutation
Genes