Papers - SUZUKI Nobuaki
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A case of MYH9 disorders caused by a novel mutation (p.K74E) Reviewed
Kanematsu, T. Suzuki, N. Yoshida, T. Kishimoto, M. Aoki, T. Ogawa, M. Kagami, Y. Kiyoi, H. Matsushita, T. Kunishima, S.
Ann Hematol Vol. 95 ( 1 ) page： 161-3 2015.9
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Acquired von Willebrand syndrome in a patient with immune thrombocytopenic purpura Reviewed
Ihara, A. Suzuki, N. Matsushita, T. Ichinose, A.
Rinsho Ketsueki Vol. 56 ( 7 ) page： 901-4 2015.8
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The features of clearance in recombinant factor IX (BeneFIX((R)) ) Reviewed
Suzuki, N. Takedani, H. Hirakawa, A. Ushijima, Y. Matsushita, T.
Haemophilia Vol. 21 ( 5 ) page： 702-7 2015.4
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Endoscopic treatment of esophageal varices in hemophiliac patients with liver cirrhosis Reviewed
Ishizu, Y. Ishigami, M. Suzuki, N. Kuzuya, T. Honda, T. Hayashi, K. Katano, Y. Hirooka, Y. Ishikawa, T. Matsushita, T. Goto, H.
Gastrointest Endosc Vol. 81 ( 4 ) page： 1059-60 2015.3
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Rhof promotes murine marginal zone B cell development Reviewed
Kishimoto, M. Matsuda, T. Yanase, S. Katsumi, A. Suzuki, N. Ikejiri, M. Takagi, A. Ikawa, M. Kojima, T. Kunishima, S. Kiyoi, H. Naoe, T. Matsushita, T. Maruyama, M.
Nagoya J Med Sci Vol. 76 ( 3-4 ) page： 293-305 2015.3
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Hepatectomy for hepatocellular carcinoma in patients with hemophilia Reviewed
Inokawa, Y. Sugimoto, H. Kanda, M. Yamada, S. Fujii, T. Nomoto, S. Takeda, S. Suzuki, N. Matsushita, T. Kodera, Y.
J Hepatobiliary Pancreat Sci Vol. 21 ( 11 ) page： 824-8 2014.8
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Animal models of MYH9 disorders Invited Reviewed
Suzuki, N. Kunishima, S. Naoe, T. Matsushita, T.
Rinsho Ketsueki Vol. 54 ( 11 ) page： 2031-7 2013.12
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Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability Reviewed
Suzuki, N. Kunishima, S. Ikejiri, M. Maruyama, S. Sone, M. Takagi, A. Ikawa, M. Okabe, M. Kojima, T. Saito, H. Naoe, T. Matsushita, T.
PLoS One Vol. 8 ( 8 ) page： e71187 2013.8
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A possible mechanism for Inv22-related F8 large deletions in severe hemophilia A patients with high responding factor VIII inhibitors Reviewed
Fujita, J. Miyawaki, Y. Suzuki, A. Maki, A. Okuyama, E. Murata, M. Takagi, A. Murate, T. Suzuki, N. Matsushita, T. Saito, H. Kojima, T.
J Thromb Haemost Vol. 10 ( 10 ) page： 2099-107 2012.8
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Successful fertility management of a patient with factor V deficiency: planned transfusion of fresh frozen plasma under infertility treatment Reviewed
Iwase, A. Goto, M. Manabe, S. Hirokawa, W. Kobayashi, H. Nakahara, T. Takikawa, S. Kotani, T. Sumigama, S. Tsuda, H. Nakayama, T. Suzuki, N. Matsushita, T. Kikkawa, F.
Fertil Steril Vol. 95 ( 6 ) page： 2124.e5-7 2011.2
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Severe hemophilia A in a Japanese female caused by an F8-intron 22 inversion associated with skewed X chromosome inactivation Reviewed
Miyawaki, Y. Suzuki, A. Fujimori, Y. Takagi, A. Murate, T. Suzuki, N. Katsumi, A. Naoe, T. Yamamoto, K. Matsushita, T. Takamatsu, J. Kojima, T.
Int J Hematol Vol. 92 ( 2 ) page： 405-8 2010.8
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Heterozygous antithrombin deficiency improves in vivo haemostasis in factor VIII-deficient mice Reviewed
Bolliger, D. Szlam, F. Suzuki, N. Matsushita, T. Tanaka, K. A.
Thromb Haemost Vol. 103 ( 6 ) page： 1233-8 2010.3