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  <title>DSpace コレクション: 1994-06</title>
  <link rel="alternate" href="http://hdl.handle.net/10564/1653" />
  <subtitle>1994-06</subtitle>
  <id>http://hdl.handle.net/10564/1653</id>
  <updated>2026-04-09T03:44:38Z</updated>
  <dc:date>2026-04-09T03:44:38Z</dc:date>
  <entry>
    <title>セボフルランのネコ局所脳血流量及び炭酸ガス反応性に及ぼす影響</title>
    <link rel="alternate" href="http://hdl.handle.net/10564/1695" />
    <author>
      <name>右衛門佐, 博千代</name>
    </author>
    <id>http://hdl.handle.net/10564/1695</id>
    <updated>2017-05-29T06:07:45Z</updated>
    <published>1994-06-29T15:00:00Z</published>
    <summary type="text">タイトル: セボフルランのネコ局所脳血流量及び炭酸ガス反応性に及ぼす影響
著者: 右衛門佐, 博千代
抄録: We evaluated the effect of 1% and 2% of sevoflurane with nitrous oxide, oxygen on the regional cerebral blood flow (rCBF) and CO₂ reactivity in cats. The 12 cats were divided into 3 groups : the control group nitrous oxide, oxygen, 1% sevoflurane group&#xD;
and 2% sevoflurane group. The rCBF were measured by Laser Doppler Flowmetry in the&#xD;
steady-state of hypocapnia, normocapnia, and hypercapnia by regulation of inspired CO₂&#xD;
concentration in all groups. The rCBF under 1% and 2% sevoflurane significantly decreased to 26±9 ml/100 g/min, and 27±9 ml/100 g/min respectively compared with the&#xD;
control group (30±9 ml/100 g/min). But the CO₂ reactivity (ΔrCBF/ΔCO₂) remained under 1% and 2% sevoflurane anesthesia.</summary>
    <dc:date>1994-06-29T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>卵白によるアレルギーが成因と考えられる膵炎の一例</title>
    <link rel="alternate" href="http://hdl.handle.net/10564/1694" />
    <author>
      <name>豊島, 桂次</name>
    </author>
    <id>http://hdl.handle.net/10564/1694</id>
    <updated>2017-05-29T06:07:42Z</updated>
    <published>1994-06-29T15:00:00Z</published>
    <summary type="text">タイトル: 卵白によるアレルギーが成因と考えられる膵炎の一例
著者: 豊島, 桂次
抄録: A 40-year-old man who had occasionally felt abdominal pain due to unknown causes since his childhood was treated under the　provisional diagnosis of ideopathic　pancreatitis, because the increases of elastase Ⅰ were simultaneously related to his abdominal complaint without any other findings such as lithiasis, gastrointestinal disease, hyperparathyroidism etc. One day, soon after eating sukiyaki, he suffered from severe epigastralgia more than before. Next day, the laboratory date revealed that the IgE-RAST for egg white was positive and the ratio of eosinocytes in the patient's white blood cells was high, additionally increasing lipase, trypsin and elastase Ⅰ in serum. These clinical features suggest that this case of pancreatitis is related to an allergic reaction by egg white.</summary>
    <dc:date>1994-06-29T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>PRIMARY OVARIAN MYXOMA</title>
    <link rel="alternate" href="http://hdl.handle.net/10564/1693" />
    <author>
      <name>Noda, Tsuneo</name>
    </author>
    <author>
      <name>Harada, Naoya</name>
    </author>
    <author>
      <name>Ueda, Gaiko</name>
    </author>
    <author>
      <name>Onishi, Yasuhiko</name>
    </author>
    <author>
      <name>Hino, Kouji</name>
    </author>
    <author>
      <name>Tokui, Hiroshi</name>
    </author>
    <id>http://hdl.handle.net/10564/1693</id>
    <updated>2017-06-11T23:20:26Z</updated>
    <published>1994-06-29T15:00:00Z</published>
    <summary type="text">タイトル: PRIMARY OVARIAN MYXOMA
著者: Noda, Tsuneo; Harada, Naoya; Ueda, Gaiko; Onishi, Yasuhiko; Hino, Kouji; Tokui, Hiroshi
抄録: Primary ovarian myxoma is exceedingly rare, with only five cases known to be reported. We present an 18-year-old female with an ovarian myxoma.</summary>
    <dc:date>1994-06-29T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>麻痺性イレウスと腹水を伴った虚血性腸炎が発症したSLEの1例</title>
    <link rel="alternate" href="http://hdl.handle.net/10564/1692" />
    <author>
      <name>西浦, 公章</name>
    </author>
    <author>
      <name>川野, 貴弘</name>
    </author>
    <author>
      <name>澤井, 伸之</name>
    </author>
    <author>
      <name>鶴田, 俊介</name>
    </author>
    <author>
      <name>森岡, 泰子</name>
    </author>
    <author>
      <name>山野, 繁</name>
    </author>
    <author>
      <name>土肥, 和紘</name>
    </author>
    <id>http://hdl.handle.net/10564/1692</id>
    <updated>2017-05-29T06:07:44Z</updated>
    <published>1994-06-29T15:00:00Z</published>
    <summary type="text">タイトル: 麻痺性イレウスと腹水を伴った虚血性腸炎が発症したSLEの1例
著者: 西浦, 公章; 川野, 貴弘; 澤井, 伸之; 鶴田, 俊介; 森岡, 泰子; 山野, 繁; 土肥, 和紘
抄録: A case of systemic lupus erythematosus complicated by ischemic enteritis with paralytic ileus and ascites is reported. The patient was a 39-year-old female. A diagnosis of SLE was made in January 1991. Her condition was maintained with low doses&#xD;
of prednisolone (5 mg/day). She was admitted to our hospital because of abdominal pain&#xD;
on August 1, 1992. US and plain film of the abdomen disclosed the existence of ischemic&#xD;
enteritis, ileus and ascites. Low CH50 was seen in July 2, 1992. She was treated with high doses of prednisolone (40 mg/day) and recoverd 20 days later. The present case indicates that intestinal lesion and lower CH50 were markers of the active stage.</summary>
    <dc:date>1994-06-29T15:00:00Z</dc:date>
  </entry>
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