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- hypokalemic alkalosis 缺钾性碱中毒
- hypokalemic alkalosis syndrome 低钾血性硷中毒综合征
- Alkalosis and potassium depletion may be pronounced. 可能有碱中毒和缺钾。
- Hypernatremia and metabolic alkalosis did not occur. 血尿素氮、肌酐等清除理想。
- Application of excessive hours, can cause metabolic alkalosis. 应用过量时，可致代谢性碱中毒。
- The patients were hypokalemic during 6.5 years on the average. 这些患者低钾血症的时间平均为6.;5年。
- Increased renal excretion occurs with both respiratory and metabolic alkalosis. 在呼吸性碱中毒和代谢性碱中毒中钾离子的肾排泄增加。
- Status suggests a mixed metabolic acidosis and respiratory alkalosis. 病人的酸碱平衡状态提示混合性代谢性酸中毒和呼吸性碱中毒。
- Metabolic acidosis had the same occurrence with metabolic alkalosis. 呼酸型＞呼碱型，代酸与代碱基本相当；
- Thus, in alkalosis, the increased potassium ion excretion in exchange for sodium ion permits hydrogen ion conservation. 因此在碱中毒中，钠钾交换的增加使氢离子保留。
- Of the total 168 patients , 121(72.0%) had TABD of respiratory alkalosis, 47(28.0%) had TABD of respiratory acidosis . 168例中呼吸性碱中毒合并代谢性碱中毒并代谢性酸中毒 (呼碱型TABD) 12 1例 (72 0%25 ) ; 呼吸性酸中毒合并代谢性碱中毒并代谢性酸中毒 (呼酸型TABD) 4 7例 (2 8 0%25 )。
- They have typical laboratory findings, including hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria. 在此篇文章中，我们将报告三个病例：一是偶发性个案，另两位是姐弟。
- Arterial blood gas (ABG) analysis demonstrates mild hypoxemia and respiratory alkalosis. 动脉血气分析显示轻度低氧血症和呼吸性碱中毒。
- Kempf R,Wegmann D.Periodic hypokalemic paralysis in thyrotoxicosis[J].Schweiz Med Wochenschr,1993,123:1843. Kempf R,Wegmann D.甲状腺功能亢进症伴低钾周期性麻痹[J].Schweiz Med Wochenschr,1993,123:1843.
- Kempf R, Wegmann D. Periodic hypokalemic paralysis in thyrotoxicosis. S chweiz Med Wochenscher, 1993, 123:1843. 赵党生.;甲状腺机能亢进症并发周期性麻痹文献复习(附7例报告)
- He seizured within fifteen minutes of his arrival and was found to have acute respiratory alkalosis. 在他抵达急诊室后的十五分钟时，忽然发生惊厥及呼吸性碱中毒。
- Chronic respiratory alkalosis( CRA), CRA plus metabolic alkalosis and metabolic acidosis are seldom. 慢性呼吸性碱中毒、性呼吸性碱中毒并代谢性碱中毒和代谢性酸中毒是少见的。
- Results 71.43% of rise in creatine phosphokinase of the idiopathic hypokalemic periodic paralysis. 结果原发性低钾型周期性麻痹患者血清肌酸激酶增高占71.;43%25;血清肌酸激酶改变呈现一定规律。
- Conclusion The heredity in hypokalemic periodic paralysis is of genetic heterogeneity. 结论低钾性周期性麻痹的遗传存在异质性。
- The outstanding laboratory features were hypochloremic alkalosis and severe hypokalemia. 实验室检查发现有代谢性碱血症、低血钾症及低血氯症。
