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hbh

  • 血红蛋白;【医】hemoglobin-H 血红蛋白H
hbhhbh
  1. Methods : 624 cases with HBH in 1997-2000 from our hospital were analyzed with circular distribution theory .

    方法:病例系1997-01~2000-12我院收治的佳木斯地区的脑出血患者624例,采用圆形分布理论,统计分析脑出血的发生和时间分布的关系。

  2. Organization of a-Globin Genes in Chinese with HbH Diseases in Guangdong Province

    我国广东地区HbH病人的α-珠蛋白基因组织

  3. Cases with HbH disease were detected .

    HbH病6例。

  4. Objective : To study time distribution of occurrence of hypertensive brain hemohage ( HBH ) .

    目的:脑出血发病的时间分布。

  5. The synthetic monomers were optimized and the gas hydrate called HBH was developed in emulsion polymerization .

    采用乳液聚合方式,通过正交实验研究得到了最佳合成条件,研制出天然气水合物动力学抑制剂HBH。

  6. Conclusion HbH band (β 4 ) sometimes could not be detected in Hemoglobin H disease combined with β thalassemia .

    结论血红蛋H病复合β地贫时可检测不到HbH(β4)区带。

  7. HBH Smart Li-ion Battery Pack is the best choice as a green power for various electro-thermal costume .

    HBH智能聚合物锂电池组是当今各类电热服装最优的绿色环保能源。

  8. Methods 60 patients with HBH were classified randomly into PCA group and CAT ( conventional analgesia therapy ) group , each of the groups had 30 patients .

    方法60例HBH手术病人随机分为病人自控镇痛(PCA)组和传统镇痛(CAT)组,每组30例。

  9. In this paper , synthetic technology of hydrate inhibitor HBH is presented and its inhibitive property and compatibility with other additives are also evaluated in laboratory .

    介绍了水合物抑制剂HBH的合成工艺,对其水合物抑制性及与其它处理剂的配伍性进行了室内评价。

  10. Results showed that the hydrate forming is effectively suppressed when a few hydrate inhibitor HBH ( about 0 . 5 % ) was added into the drilling fluid .

    结果表明,加入少量水合物抑制剂HBH于钻井液(约为0.5%)中即能有效地抑制水合物的生成;

  11. Methods : 21 cases of HbH disease and 442 clinical uncertain cases were detected by the single-tube multiplex-PCR assay , and 2 cases were detected with amniotic fluid .

    方法采用单管多重PCR体系对21例血红蛋白H病和442例临床送检病例血样本进行α地中海贫血基因诊断,另2例取羊水进行产前诊断。

  12. Methods α globin gene tissue of 124 cases with HbH disease were analyzed by Southern blot hybridization , restriction mapping of PCR products , hemoglobin electrophoresis and Long PCR technology .

    方法应用Southern印迹杂交、限制性内切酶分析PCR产物、血红蛋白电泳和longPCR等技术,对受检HbH病患者的α珠蛋白基因组织进行了鉴定。

  13. Objective : To observe the healing effects of clearing out intracranial hematoma ( CIH ) by drilling skull to treat hypertensive brain hemorrhage ( HBH ) .

    目的:进一步评价钻颅血肿抽吸治疗高血压脑出血的疗效及时机的选择。

  14. Evaluating results indicate that HBH has a good inhibiting property and has small impact on the mud rheology and filtration loss when added percentage of HBH is less than 0.5 % .

    评价结果表明,HBH具有良好的抑制性且在加量小于0.5%时对水基钻井液的流变性和滤失量影响不大。

  15. Homozygote β - thalassemia was prone to iron overload , followed by non-deletion HbH diseases , at the occurrence rate of 79.2 % and 27.3 % respectively .

    最易发生铁负荷过重的是纯合子β地中海贫血(79.2%),次之为非缺失型HBH(27.3%)。

  16. Objective To analyze the molecular abnormalities as well as the distribution of α globin genes in 124 cases with HbH disease ; and provide scientific basis for molecular diagnosis and prenatal diagnosis in this hemoglobin disorder .

    目的分析124例HbH患者的α珠蛋白基因的分子缺陷状况及其分布,为HbH的基因诊断和产前诊断提供科学依据。

  17. Results There were 61 cases of α thalassemia in all patients group , in of which 55 cases of standard types were α thalassemia heterozygotes , genotypes α α / SEA , 6 cases of HbH which genotypes were α - / deletion .

    结果本组病例共检出61例α地贫,其中55例标准型α地贫均为α地贫1杂合子,基因型αα/SEA,6例HbH病基因型α-/缺失型。

  18. Conclusion The molecular abnormalities of α globin genes in HbH patients were significantly different in different regions . This study provides useful knowledge for the understanding the molecular genetics of HbH disease as well as for molecular diagnosis in the regions where the disease is prevalent .

    结论不同地区HbH患者的α珠蛋白基因的突变类型有明显的差异,该项研究为HbH病的分子遗传学和HbH病的基因诊断提供了依据。