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Ophthalmology. Retina|June 4, 2023
Macular Retinoschisis from Optic Disc without a Visible Optic Pit or Advanced Glaucomatous Cupping (No Optic Pit Retinoschisis [NOPIR])Satoko Fujimoto, Gregg T Kokame, Edwin H Ryan, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 2002
Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activityKoichi Kokame, Masanori Matsumoto, Kenji Soejima, et al.
Brain Research|December 28, 2010
Gene expression associated with an enriched environment after transient focal ischemiaYuji Shono, Chiaki Yokota, Yuji Kuge, et al.
Cancer Research|May 19, 2006
Evolution of the androgen receptor pathway during progression of prostate cancerPeter J M Hendriksen, Natasja F J Dits, Koichi Kokame, et al.
Scientific Reports|October 19, 2017
Herpud1 negatively regulates pathological cardiac hypertrophy by inducing IP3 receptor degradationNatalia Torrealba, Mario Navarro-Marquez, Valeria Garrido, et al.
International Journal of Hematology|September 9, 2023
Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) in Japan 2023Masanori Matsumoto, Yoshitaka Miyakawa, Koichi Kokame, et al.
Neuroscience Letters|April 5, 2011
Gene and protein analysis of brain derived neurotrophic factor expression in relation to neurological recovery induced by an enriched environment in a rat stroke modelKenji Hirata, Yuji Kuge, Chiaki Yokota, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|April 3, 2024
[Congenital thrombotic thrombocytopenic purpura diagnosed in adulthood after repeated thrombocytopenia since neonatal period]Teruhiko Yoshino, Takuro Kuriyama, Sae Utsumi, et al.
Artificial Organs|January 12, 2016
Influence of a Rotational Speed Modulation System Used With an Implantable Continuous-Flow Left Ventricular Assist Device on von Willebrand Factor DynamicsNoritsugu Naito, Toshihide Mizuno, Takashi Nishimura, et al.
Clinical and Experimental Nephrology|March 8, 2018
Clinical characteristics and genetic backgrounds of Japanese patients with atypical hemolytic uremic syndromeMadoka Fujisawa, Hideki Kato, Yoko Yoshida, et al.
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