Han Y, Kato M, Ashihara N, Higuchi Y, Matoba H, Wang W, Hayashi H, Itoh Y, Takahashi S, Kurita H, Nakayama J, Okumura N, Hiratsuka S. Citrullinated fibrinogen-SAAs complex causes vascular metastagenesis. Nature Communications. 2023. 14. 1. 4960
Kaido T, Yoda M, Kamijo T, Arai S, Taira C, Higuchi Y, Okumura N. A novel amino acid substitution, fibrinogen Bbetap.Pro234Leu, associated with hypofibrinogenemia causing impairment of fibrinogen assembly and secretion. Int. J. Mol. Sci. 2021. 21. 9422; doi:10.3390/ijms21249422
Osada M, Maruyama K, Kokame K, Denda R, Yamazaki K, Kunieda H, Hirao M, Madoiwa S, Okumura N, Murata M, Ikeda Y, Watanabe K, Tsukada Y, Kikuchi T. A novel homozygous variant of the thrombomodulin gene causes a hereditary bleeding disorder. Blood Advance. 2021. 5. 3830-3838
Arai S, Kamijo T, Kaido T, Yoda M, Shinohara S, Suzuki T, Arai N, Sugano M, Uehara T, Okumura N. Automated screening procedure for phenotype of congenital fibrinogen disorder using novel parameters, |min1|c and Ac/|min1|c obtained from clot waveform analysis of Clauss method. Clinica Chimica ACTA. 2021. 521. 170-176
Yoda M, Kaido T, Kamijo T, Taira C, Higuchi Y, Arai S, Okumura N. Novel variant fibrinogen gammap.C352R produced hypodysfibrinogenemia leading to a bleeding episode and failure of infertility treatment. Int J Hematology. 2021. 114. 325-333
International Society for Thrombosis and Haemostasis
, International Fibrinogen Research Society
, 日本臨床検査自動化学会
, 日本検査血液学会
, 日本血栓止血学会
, 臨床化学会
, 日本臨床検査医学会
