Genetic abnormalities of Bernard-Soulier Syndrome von KUNISHIMA, Shinji, KAMIYA, Tadashi, SAITO, Hidehiko

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Presence of Propionibacterium acnes in blood components von Kunishima, Shinji, Inoue, Chikako, Kamiya, Tadashi, Ozawa, Kazuo

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Epitope Analysis of Antibodies in Japanese to Human Cytomegalovirus Phosphoprotein 150 with Synthetic Peptides von TAKAHASHI, Isao, SUGIURA, Sayoko, OHTA, Hirotoshi, OZAWA, Kazuo, KAMIYA, Tadashi

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Clinical trial to investigate the pharmacokinetics, pharmacodynamics, safety, and efficacy of recombinant factor VIIa in Japanese patients with hemophilia with inhibitors von SHIRAHATA, Akira, KAMIYA, Tadashi, NAKA, Hiroyuki, FUJITA, Shigeru, MINAMOTO, Yoko, KAMIZONO, Junji, SAITO, Hidehiko, TAKAMATSU, Junki, KOJIMA, Tetsuhito, FUKUTAKE, Katsuyuki, ARAI, Morio, HANABUSA, Hideji, TAGAMI, Hisamichi, YOSHIOKA, Akira, SHIMA, Midori

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Homozygous Pro74 → Arg Mutation in the Platelet Glycoprotein Ibβ Gene Associated with Bernard-Soulier Syndrome von Kunishima, Shinji, Tomiyama, Yoshiaki, Honda, Shigenori, Fukunishi, Mariko, Hara, Junichi, Inoue, Chikako, Kamiya, Tadashi, Saito, Hidehiko

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Immunofluorescence Analysis of Neutrophil Nonmuscle Myosin Heavy Chain-A in MYH9 Disorders: Association of Subcellular Localization with MYH9 Mutations von Kunishima, Shinji, Matsushita, Tadashi, Kojima, Tetsuhito, Sako, Masahiro, Kimura, Fumihiro, Jo, Eun-Kyeong, Inoue, Chikako, Kamiya, Tadashi, Saito, Hidehiko

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Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome) von KUNISHIMA, Shinji, KOJIMA, Tetsuhito, KAMIYA, Tadashi, SAITO, Hidehiko, MATSUSHITA, Tadashi, TANAKA, Toshihiro, TSURUSAWA, Masahito, FURUKAWA, Yoshio, NAKAMURA, Yukitsugu, OKAMURA, Takashi, AMEMIYA, Norihiko, NAKAYAMA, Takayuki

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Clinical Evaluation of Repeat Apheresis Donors in Japan von Furuta, Motomu, Shimizu, Tetsuo, Mizuno, Shinichi, Kamiya, Tadashi, Ozawa, Kazuo, Nakase, Toshie, Tadokoro, Kenji, Takenaka, Michiko, Ohkawa, Tsutomu, Yokoyama, Shigeki, Ogawa, Yoshiaki, Kiyokawa, Hiroyuki, Shimizu, Masaru, Sekine, Naoki, Yoshimura, Isao

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Determination of Glycocalicin in Platelet Concentrate Supernatants Stored in a Synthetic Medium (Seto Solution) von Kunishima, Shinji, Shimizu, Tetsuo, Kora, Shinichi, Kamiya, Tadashi, Ozawa, Kazuo

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Interaction of von Willebrand Factor with the Extracellular Matrix and Glycocalicin under Static Conditions von Matsui, Taei, Kunishima, Shinji, Hamako, Jiharu, Katayama, Masahiko, Kamiya, Tadashi, Naoe, Tomoki, Ozeki, Yasuhiro, Fujimura, Yoshihiro, Titani, Koiti

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Identification of six novel MYH9 mutations and genotype–phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions von Kunishima, S., Matsushita, T., Kojima, T., Amemiya, N., Choi, Y. M., Hosaka, N., Inoue, M., Jung, Y., Mamiya, S., Matsumoto, K., Miyajima, Y., Zhang, G., Ruan, C., Saito, K., Song, K. S., Yoon, H.-J., Kamiya, T., Saito, H.

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VISUAL IDENTIFICATION OF Serratia liquefaciens-CONTAMINATED RED BLOOD CELLS von Sugiura, Sayoko, Yamada, Takayoshi, Inoue, Chikako, Nakashima, Syozo, Ozawa, Kazuo, Kamiya, Tadashi

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Novel heterozygous missense mutation in the platelet glycoprotein Ibβ gene associated with isolated giant platelet disorder von Kunishima, Shinji, Naoe, Tomoki, Kamiya, Tadashi, Saito, Hidehiko

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GATA-2 transcription factor is mutated in CMK magakaryoblastic cell line von Kunishima, Shinji, Kojima, Tetsuhito, Inoue, Chikako, Kamiya, Tadashi, Hidehiko Saito

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Missense mutations of the glycoprotein (GP) Ibβ gene impairing the GPIb α/β disulfide linkage in a family with giant platelet disorder von KUNISHIMA, S, LOPEZ, J. A, KOBAYASHI, S, IMAI, N, KAMIYA, T, SAITO, H, NAOE, T

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Novel nonsense mutation in the platelet glycoprotein Ibβ gene associated with Bernard‐Soulier syndrome von Kunishima, Shinji, Matsushita, Tadashi, Ito, Takahiko, Kamiya, Tadashi, Saito, Hidehiko

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Novel nonsense mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndrome von Kunishima, Shinji, Matsushita, Tadashi, Ito, Takahiko, Kamiya, Tadashi, Saito, Hidehiko

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Mapping of a gene for May-Hegglin anomaly to chromosome 22q von KUNISHIMA, S, KOJIMA, T, TANAKA, T, KAMIYA, T, OZAWA, K, NAKAMURA, Y, SAITO, H

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A QUESTIONNAIRE SURVEY ON PREVENTIVE MEASURES TO EXCLUDE DONORS WITH POTENTIAL HIV INFECTION FROM BLOOD DONATIONS von Takenaka, Michiko, Shimizu, Masaru, Ikeda, Hisami, Kamiya, Tadashi, Inoue, Chikako

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FEASIBILITY AND SAFETY OF RED CELL COLLECTION BY APHERESIS TECHNOLOGY von Yamamoto, Sadamitsu, Kamiya, Tadashi, Shibata, Hitoshi, Maeda, Yoshiaki, Hiruma, Kiyoshi, Komatsu, Fumio, Ikeda, Hisami, Shimizu, Masaru

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