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pro vyhledávání: '"Nobuhiko Yoshida"'
We administered AT III concentrates to 21 patients with DIC who failed to respond initially to heparin therapy. About 60% of these 21 patients were effectively treated with AT III concentrates by enhancing the effect of heparin and alleviating the bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c12e23eb940a4a8d418d2bc0ba6b1c4
https://doi.org/10.1159/000408471
https://doi.org/10.1159/000408471
Autor:
Kazuki Niwa, Nobuhiko Yoshida, Masazumi Sameshima, Jun Mimuro, Akira Nagita, Teruko Sugo, John W. Weisel, Michio Matsuda, Chizuko Nakamikawa
Publikováno v:
Blood. 96:3779-3785
The authors have identified a 12-residue carboxyl-terminal extension of Lys-Ser-Pro-Met-Arg-Arg-Phe-Leu-Leu-Phe-Cys-Met in a dysfibrinogen derived from a woman heterozygotic for this abnormality and associated with severe bleeding. This extension is
Autor:
Nobuhiko Yoshida
Publikováno v:
Japanese journal of MHTS. 26:390-397
眼圧が高い人への生活指導の参考にするため, 眼圧値と人間ドックの各種検査成績を比較検討した。眼圧平均値および高眼圧率 (眼圧が20以上の割合) は女性より男性の方が有意に高かっ
Autor:
Kensuke Yamazumi, Michio Matsuda, Teruko Sugo, Kazuki Niwa, Nobuhiko Yoshida, Shigeharu Terukina, Hisato Maekawa
Publikováno v:
Thrombosis and Haemostasis. 82:283-290
Introduction: Hereditary dysfibrinogen is a fibrinogen molecule that is unable to exert its physiological functions due to a structural alteration(s) determined at the gene level. The functions may be inherent in the molecule, as represented by fibri
Publikováno v:
Hepatology Research. 12:233-239
Clear evidence for TT virus (TTV) to be a hepatitis virus remains unseen despite its origination from a hepatitis patient. Epidemiological studies on TTV have been limited more or less by the prematurity of the diagnostic systems. We sought after PCR
Autor:
M. Matsushita, Kuniaki Nakao, Masahiro Matsumoto, K. Iwata, Yasuhiko Ohta, Minako Hijikata, Koichi Kanai, Nobuhiko Yoshida, Kiyoshi Baba, Shunji Mishiro
Publikováno v:
Archives of Virology. 143:645-651
We assessed the genetic polymorphism of mannose-binding lectin (MBL) in 93 patients with chronic hepatitis C (45 responders and 48 nonresponders to interferon) and 218 healthy controls. Mutant allele was identified only at codon 54 (Gly--Asp), leadin
Autor:
Koichi Kanai, H Matsumoto, Takamasa Miyake, Nobuhiko Yoshida, Masahiro Matsumoto, Kuniaki Nakao, K. Iwata
Publikováno v:
Journal of Gastroenterology. 30:244-247
A 70-year-old woman with myeloproliferative disorder and massive splenomegaly presented with hematemesis. Emergency endoscopy demonstrated bleeding from esophageal varices. Management of variceal hemorrhage by endoscopic injection sclerotherapy, usin
Publikováno v:
Thrombosis and Haemostasis. 68:534-538
SummaryCongenitally abnormal fibrinogen Osaka III with the replacement of γ Arg-275 by His was found in a 38-year-old female with no bleeding or thrombotic tendency. Release of fibrinopeptide(s) by thrombin or reptilase was normal, but her thrombin
Autor:
Minoru Okuma, Nobuhiko Yoshida, Shinji Asakura, Michio Matsuda, Kensuke Yamazumi, Hajime Hirata
Publikováno v:
Blood. 78:149-153
A new case of heterozygous dysfibrinogenemia characterized by an amino acid replacement in the NH2-terminal region of the fibrin alpha-chain was found in a 27-year-old woman with a bleeding problem. Her one-stage prothrombin time and activated partia
Autor:
Hajime Hirata, Shigeru Shirakawa, Kensuke Yamazumi, Hideo Wada, Michio Matsuda, Nobuhiko Yoshida, Shinji Asakura, Koichi Morita
Publikováno v:
Blood. 77:1958-1963
A new case of heterozygous dysfibrinogenemia characterized by the replacement of NH2-terminal amino acid of fibrin beta-chain was found in a 50-year-old man. Despite a prolonged thrombin time, the propositus' fibrinogen had a normal reptilase time wi