Author

Ryunosuke Denda

Institution: Saiseikai Central Hospital

Observed institution: Saiseikai Central Hospital

ORCID: 0000-0002-4661-7394

Observed ORCID: 0000-0002-4661-7394

OpenAlex ID: A5039422392

A novel homozygous variant of the thrombomodulin gene causes a hereditary bleeding disorder

2021 · Makoto Osada, Keiko Maruyama, et al. · Blood Advances · 16

Negative E-cadherin expression on bone marrow myeloma cell membranes is associated with extramedullary disease

2022 · Maki Hirao, Kohei Yamazaki, et al. · F1000Research · 7

Rare evolution of CSF3R-mutated chronic neutrophilic leukemia to t(4;12)(q12;p13) acute myeloid leukemia with SETBP1 mutation

2022 · Maki Hirao, Kentaro Watanabe, et al. · Leukemia Research Reports · 2

Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia Incidentally Detected by Fluorodeoxyglucose-positron Emission Tomography/Computed Tomography at a Health Checkup

2022 · Hisako Kunieda, Ryunosuke Denda, et al. · Internal Medicine · 1

[PAX5-positive plasma cell leukemia presenting as lymphocytosis].

2022 · Suzuka Tateno, Maki Hirao, et al. · PubMed · 1

Works count: 5

Citation count: 27

H-index: 2

I10-index: 1