查询词典 family history

Lacunae and defect signs in the respiratory tract may indicate various inherent disease backgrounds such as allergies and rheumatoid arthritis in the family history.

呼吸 的广阔地面的 Lacunae 和缺点告示可能指出各种不同的固有背景，像是过敏症和家庭历史的风湿性关节炎。

Methods Pedigrees of microtia were collected through inquiring family history. Then cell genetics analysis and molecular genetics research were carried on.

通过对住院患者及其家属家族史的询问调查，收集先天性小耳畸形家系；利用收集的家系资源进行先证者核型分析和vrk1基因突变检测。

Objective To explore the relationship between 3'-variable numble of tandem repeats (3'-VNTR) of apolipoproteins B and cerebral hemorrhage with family history in Changsha Han Chinese.

目的 探讨载脂蛋白B(apolipoproteins B， apoB)基因3'端可变数目串联重复序列(3'-variable numble of tandem repeats， 3'-VNTR)多态性与长沙地区汉族人群家族聚集性脑出血的关系。

Amongst these, 26 had symptoms compatible with spinal cord involvement. However, two cases with primary progressive pyramidal paraparesis were excluded because after the diagnostic work-up they were found out to have other possible underlying causes (one had constrictive meningeal thickening because of a very remote subarachnoid haemorrhage, and the other had positive family history suggesting an autosomal dominant disorder).

其中，26例有脊髓受累症状，但其中有2例表现为原发进展性痉挛性截瘫的患者，其症状可以用白塞病以外的其他原因来解释，因此，这2例患者被排除在本研究之外（1例患者因蛛网膜下腔出血而出现脑膜增厚，另1例患者因有阳性家族史而怀疑为常染色体显性遗传性疾病--遗传性痉挛性截瘫）。

Presymptomatic genetic screening : Presymptomatic genetic screening may be appropriate for persons with a family history of a dominantly inherited disorder （eg, Huntington's disease, breast cancer）.

症状前遗传筛查适用于家族史中有显性遗传病的人（如遗传性舞蹈病，乳腺癌）。

Presymptomatic genetic screening : Presymptomatic genetic screening may be a ropriate for perso with a family history of a dominantly inherited disorder （eg, Huntington's disease, breast cancer）.

症状前遗传筛查适用于家族史中有显性遗传病的人（如遗传性舞蹈病，乳腺癌）。

By 2001, McGlashan and his team had completed their "Structured Interview for Prodromal Symptoms"— a two-hour assessment involving various oral tests and a family history.

到2001年为止，McGlashan 和他的小组已经完成了他们的&病前症状结构化面试&（SIPS--这是一次两小时、涉及各种口头测试和家庭历史的评估。

Dr. Sharma and colleagues used the Structured Clinical Interview for the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition to reinterview 61 patients diagnosed with unipolar depression who had failed to respond to at least two adequate courses of antidepressants. By examining their symptoms over time as well as their family history, the researchers discovered that 35% of these patients had a form of bipolar disorder. Even more remarkably, after following them for a year, fully 80% of patients were deemed to have bipolar disorder.

Sharma博士与其同事使用精神异常诊断与统计手册第四版的结构式临床面谈，针对61位被诊断为单极性异常，而且至少对两种以上抗忧郁药物，在使用足够疗程下，没有反应的病患进行再次面谈；透过检查他们随著时间表现出来的症状以及家族史，研究者发现，这些病患中的35%具有双极性异常的形式；更值得注意的，在追踪一年后，将近80%的病患被视为患有双极性异常。

He has written large-scale romantism of a volume according to grandfather's family history tragedy.

他根据外祖父的家史写了一部大型的浪漫主义悲剧。

For the cases of CHD,the level of plasma endothelin-1 in these of HPIgG seropositivity is higher than that of HP seronegativity(P.05).(4) No correlation between chronic HP infection and essential hypertension,diabetes mellitus,tobacco use,age,gender,vocation,living condition ,alcohol consumption and family history was found.(5) For the cases of positive for Carbon-14 urea breath test in CHD patients, the level of plasma GLU is higher than that of negativity for Carbon-14 urea breath test (P.05).The rate of positive for Carbon-14 urea breath test in CHD patients with diabetes mellitus is significantly higher than that of CHD patients without diabetes mellitus.

结果(1)冠心病组血清HPIgG阳性率明显高于非冠心病组(45.54％vs 28.30％，P＜0.05)；(2)冠心病组C-14呼气试验阳性率明显高于非冠心病组(54.46％vs 30.19％，P＜0.01)；(3)冠心病组慢性HP感染者血浆ET-1水平明显高于非HP感染者(P＜0.05)；(4)慢性HP感染与血脂、高血压史、糖尿病史、吸烟史、年龄、性别、职业、生活环境、饮酒史以及冠心病家族史无关；(5)现症HP感染与糖尿病及空腹血糖升高有关(P＜0.05)；与血脂、高血压史、吸烟史、年龄、性别、职业、生活环境、饮酒史以及冠心病家族史无关。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。