• 23 Citations
  • 2 h-Index
20112020

Research output per year

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

Fingerprint Dive into the research topics where Kei Nishiyama is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 4 Similar Profiles

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

Research Output

  • 23 Citations
  • 2 h-Index
  • 11 Article
  • 1 Review article

Gastrointestinal symptoms as an extended clinical feature of Pierson syndrome: A case report and review of the literature

Nishiyama, K., Kurokawa, M., Torio, M., Sakai, Y., Arima, M., Tsukamoto, S., Obata, S., Minamikawa, S., Nozu, K., Kaku, N., Maehara, Y., Sonoda, K. H., Taguchi, T. & Ohga, S., Apr 15 2020, In : BMC Medical Genetics. 21, 1, 80.

Research output: Contribution to journalReview article

Open Access
  • Hyperferritinemia and acute kidney injury in pediatric patients receiving allogeneic hematopoietic cell transplantation

    Kurokawa, M., Nishiyama, K., Koga, Y., Eguchi, K., Imai, T., Oba, U., Shiraishi, A., Nagata, H., Kaku, N., Ishimura, M., Honjo, S. & Ohga, S., 2020, (Accepted/In press) In : Pediatric Nephrology.

    Research output: Contribution to journalArticle

  • Lipopolysaccharide-induced monocyte death in a novel ZnF7 domain mutation of TNFAIP3

    Imai, T., Shiraishi, A., Nishiyama, K., Ishimura, M. & Ohga, S., Jun 2020, In : Journal of Allergy and Clinical Immunology: In Practice. 8, 6, p. 2071-2074.e5

    Research output: Contribution to journalArticle

    Molecular mechanisms determining severity in patients with Pierson syndrome

    Minamikawa, S., Miwa, S., Inagaki, T., Nishiyama, K., Kaito, H., Ninchoji, T., Yamamura, T., Nagano, C., Sakakibara, N., Ishimori, S., Hara, S., Yoshikawa, N., Hirano, D., Harada, R., Hamada, R., Matsunoshita, N., Nagata, M., Shima, Y., Nakanishi, K., Nagase, H. & 4 others, Takeda, H., Morisada, N., Iijima, K. & Nozu, K., Apr 1 2020, In : Journal of Human Genetics. 65, 4, p. 355-362 8 p.

    Research output: Contribution to journalArticle

  • The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S

    Kurokawa, M., Torio, M., Okubo, K., Tocan, V., Ohyama, N., Toda, N., Ishii, K., Nishiyama, K., Mushimoto, Y., Sakamoto, R., Nakaza, M., Horie, R., Kubota, T., Takahashi, M. P., Sakai, Y., Nomura, M. & Ohga, S., Apr 1 2020, In : Molecular Genetics and Genomic Medicine. 8, 4, e1175.

    Research output: Contribution to journalArticle

    Open Access