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        <identifier>oai:jrckicn.repo.nii.ac.jp:00000216</identifier>
        <datestamp>2023-12-19T07:02:57Z</datestamp>
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          <dc:title>血友病の臨床</dc:title>
          <dc:title>Clinical observations of hemophilia</dc:title>
          <dc:creator>YOSHIOKA, Keiichiro</dc:creator>
          <dc:creator>吉岡, 慶一郎</dc:creator>
          <dc:creator>ヨシオカ, ケイイチロウ</dc:creator>
          <dc:creator>KITA, Etsuko</dc:creator>
          <dc:creator>喜多, 悦子</dc:creator>
          <dc:creator>キタ, エツコ</dc:creator>
          <dc:creator>FUROUCHI, Takashi</dc:creator>
          <dc:creator>風呂内, 充</dc:creator>
          <dc:creator>フロウチ, タケシ</dc:creator>
          <dc:creator>KITAWAKI, Tatsuo</dc:creator>
          <dc:creator>北脇, 達雄</dc:creator>
          <dc:creator>キタワキ, タツオ</dc:creator>
          <dc:creator>KAWAHARA, Koji</dc:creator>
          <dc:creator>川原, 浩二</dc:creator>
          <dc:creator>カワハラ, コウジ</dc:creator>
          <dc:creator>AMAKAWA, Yoshie</dc:creator>
          <dc:creator>尼川, 佳江</dc:creator>
          <dc:creator>アマカワ, ヨシエ</dc:creator>
          <dc:creator>IRIE, Akiko</dc:creator>
          <dc:creator>入江, 章子</dc:creator>
          <dc:creator>イリエ, アキコ</dc:creator>
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          <dc:description>Clinical and laboratory studies were established on 7 cases with hemophilia A and 2 cases with hemophilia B.&#13;
1) The age of the patients in the first visit to our clinic were less than 5 years old, except for one case. The age of their initial hemorrhagic manifestaticns appeared between 2 weeks and 11 months. Hemarthrosis, ecchymosis, oral bleeding and excessive bleeding after trauma were common manifestations in both types of hemophilia.&#13;
2) Family history were examined in three generations. Four patients of hemophilia A and one patient of hemophilia B showed sex linked recessive transmission and another cases occured sporadically.&#13;
3) The tests for the diagnosis of hemophilia were carried out as follows: a) Routine test. Clotting time, bleeding time, platelet cell count, prothrombin time and partial thromboplastin time, b) Identification tests, thromboplastin generation test and assay of factor VIII or factor IX.&#13;
Bleeding time, platelet cell count and prothrombin time in all cases of hemophilia A and B were within normal range and partial thromboplastin time was markedly prolonged. Clotting time of 5 cases with hemophilia A revealed over 60 minutes and factor VIII level showed 0 per cent. Two cases of clinically mild type showed moderate prolongation of clotting time (20 to 25 minutes) and 4-6 per cent of factor VIII. Two cases with hemo-philia B were clinically severe and their factor I revealed lower than 2 per cent.</dc:description>
          <dc:description>journal article</dc:description>
          <dc:publisher>国立医療学会</dc:publisher>
          <dc:date>1970-02</dc:date>
          <dc:type>VoR</dc:type>
          <dc:identifier>医療</dc:identifier>
          <dc:identifier>2</dc:identifier>
          <dc:identifier>24</dc:identifier>
          <dc:identifier>95</dc:identifier>
          <dc:identifier>103</dc:identifier>
          <dc:identifier>Japanese journal of National Medical Services</dc:identifier>
          <dc:identifier>AN00017113</dc:identifier>
          <dc:identifier>00211699</dc:identifier>
          <dc:identifier>https://jrckicn.repo.nii.ac.jp/records/216</dc:identifier>
          <dc:language>jpn</dc:language>
          <dc:relation>info:doi/10.11261/iryo1946.24.95</dc:relation>
          <dc:relation>一般社団法人国立医療学会</dc:relation>
          <dc:relation>https://www.nhocrc.jp/iryo/gakkai.htm</dc:relation>
          <dc:relation>医療(J-STAGE)</dc:relation>
          <dc:relation>https://www.jstage.jst.go.jp/browse/iryo1946/24/2/_contents/-char/ja/</dc:relation>
          <dc:relation>isVersionOf:http://japanlinkcenter.org/JST.Journalarchive/iryo1946/24.95</dc:relation>
          <dc:rights>©1970 一般社団法人国立医療学会</dc:rights>
          <dc:rights>本文データは学協会の許諾に基づきJ-STAGEから複製したものである</dc:rights>
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