多病的

More severe forms of altitude sickness have been identified.

现已发现高空病更多的严重类型。

Objective To explore the value of curvature plane reconstruction with multislice spiral CT in the diagnosis of lumbar vertebral arthrosis.

目的 探讨多层螺旋CT曲面重建成像在诊断腰椎小关节病中的应用价值。

Methods Potential related risk factors of ROP, such as age, sex, birth weight, FiO 2, duration of inspiring ox ygen, hyaline membrane dzsease, Apgar score, intracranial hemorrhage , recurrent apnea, broncho pulmonary dysplasia, patent ductus arteriosus were studied prospectively by univariate analysis and Logistic regression a nalysis in 135 preterm infants.

方法以 13 5例早产儿患儿为研究对象，对胎龄、性别、出生体重、吸氧时间、吸氧浓度、肺透明膜病、Apgar评分、颅内出血、支气管肺发育不良、反复呼吸暂停、动脉导管开放、眼底等进行检查。同时用单因素χ2 检验和多因素logistic回归分析筛选和判定早产儿ROP发生的危险因素。

Of the many clinical symptoms, the frequently seen are seborrheic dermatitis, proliferation of blood vessels around cornea, cheilitis, corners of mouth look wet, white, thicker than usual, black and blue with swelling, nipple hypertrophy or atrophy, and often complicated by scrotal dermatitis.

维生素B2缺乏病临床症状较多，常见的有脂溢性皮炎、角膜周围血管增生、唇炎、口角湿白增厚、青红肿、乳头肥大或萎缩，常并发有阴囊皮炎。

Through continuative evaluation and revision by investigators, clients and cases managers, the culture-sensitive Diabetes Prevention Program will be suitable for decreasing the incidence of type 2 diabetes in Taiwan.

在多面向、持续评值及修正后，此方案成为适合台湾本土的病预防计划，值得推广。

Health Secretary Jose Angel Cordoba Villalobos said."The number of cases, unfortunately, will continue to increase," he said.

卫生部长何塞·天使·科尔多瓦比·利亚洛沃斯说，"不幸的是，病例数，将继续增加，"他说。

Deciduous causes and systemic diseases, such as rickets, cretinism, hypoparathyroidism.

乳牙迟萌的原因多与全身性疾病有关，如佝偻病、克汀病、甲状旁腺功能低下症。

But the current crown prince, Sultan, is in his 80s and said to be very ill.

但现在的王储，苏尔坦，已经八十多岁且据说病得很重。

However, the research of curcumin on the kidney diseases and fibrosis is not well characterized.

然而，姜黄素在肾脏病和纤维化领域的研究尚不太多。

Objective Machado-Joseph disease/Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant neurodegenerative disorder caused by an expansion of polyglutamine tract near the C-terminus of the MJD1 gene product, ataxin-3. The precise mechanism of the MJD/SCA3 pathogenesis remains unclear.

目的 马查多-约瑟夫病/脊髓小脑共济失调3型，是由 MJD1基因产物ataxin-3的C-末端的多聚谷氨酰胺发生重复扩展突变而引起的一种常染色体显性遗传的神经退行性疾病，目前它的发病机制还不清楚。

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。