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deficiency相关的网络例句

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与 deficiency 相关的网络例句 [注:此内容来源于网络,仅供参考]

Absorption is reduced, possibly contributing to iron deficiency, osteoporosis (also related to calcium deficiency), and osteomalacia due to lack of vitamin D and absence of exposure to sunshine.

吸收功能减退,可能引起缺铁、骨质疏松症及缺乏维生素D缺乏和阳光照射所致的骨软化症。

Because it is rich in vitamin A and vitamin D, so put it as unsolicited medical supplies and health supplies, prevention and treatment of night blindness, rickets pharmaceutical effects, but also the promotion of effective drugs for tuberculosis empty calcification can also be used for vitamin A deficiency of dry eye syndrome and vitamin D deficiency osteomalacia.

由于它富含维生素A和维生素D,因此自来就把它作为医药用品和保健用品,是防治夜盲症、佝偻症的特效药剂,也是促进肺结核空洞钙化的有效药物,也可用于维生素A缺乏症的干眼症和维生素D缺乏症的软骨症。

However, in the case of overcoming a diagnosed B12 deficiency, one can follow an initial injection with oral maintenance supplementation (1 mg per day), even when the cause of the deficiency is a malabsorption problem such as pernicious anemia .

然而,在克服了诊断B12缺乏的情况下,你可以按照维修与口头补充初步注射液(每天1毫克),即使不足的原因是,如恶性贫血吸收不良的问题。

The ratios of deficiency of Fe. Ca and Zn and plumbism are relatively high, while the ratios of deficiency Mg and Cu are rather low.

开封市2~6岁儿童全血Fe、Ca、Zn缺乏和铅中毒有相当高的比率,Mg和Cu缺乏的比率较低。

Five fetuses were diagnosed with female pseudohermaphroditism (21-hydroxylase deficiency in 3 and urorectal septum malformation sequence in 2). Four fetuses were diagnosed with male pseudohermaphroditism (1 with steroid sulfatase deficiency, 1 with presumed camptomelic dysplasia, and 2 undetermined).

在这16个胎儿中有5个被诊断为女性假两性畸形(其中3个有21-羟化酶分泌不足,2个有尿道直肠隔畸形),4个被诊断为男性假两性畸形(其中1个有类固醇硫酸酯酶分泌不足,1个推测可能为弯肢性发育异常,另外2个原因未定),5个有染色体异常,2个有性逆转,核型为(46,XX+SRY)。

Rickets occurs because of a deficiency in sunlight exposure, not because of a deficiency in human milk.

佝偻病的发生原因是缺少日照,而不是因为母乳营养物质的缺失。

Our results indicate that the deficiency of dystrophin would lead to the reduction or deficiency of SG proteins, which would cause disruption/dysfunction of dystrophin-glycoprotein complex , loss of linkage between subsarcolemmal cytoskeleton and extracellular matrix which, in turn, would lead to sarcolemma instability and eventually to muscle cell necrosis.

表明dystrophin缺乏将导致包括SG在内的dystrophin相关蛋白的显著减少,DGC复合体结构破坏或功能障碍,细胞膜下骨架与细胞外基质连系的丧失,致使肌细胞膜不稳定,在肌肉收缩时容易受损,最终肌纤维变性、坏死。

She started to receive traditional Chinese medicine treatment on May 17 2008. Hodgkin's lymphoma falls into the area of scrofula, phlegm nodule, or tuberculosis of lymph node in TCM, and the mechanism is phlegm obstruction transforming into fire with stagnation of qi and blood, deficiency of liver and kidney and deficiency of both qi and yin.

本病是属於中医"痰核"、"瘰癧"、"恶核"等范畴,其病机为痰凝化火加上气血瘀结为患,就中医辨证分型而言,其病位在脾肝肾,病机在肝肾亏损、气阴两虚、痰凝兼有血瘀,并出现阴虚有热之证,秦艽鳖甲散可滋阴清热,软坚散结故作为本病主方,配合一贯煎来平补肝肾之阴,再以沙参麦冬汤来养阴生津清热。

Experimental studiesThis experiment adopts the chronic serum sickness MsPGN animal model improved and combine it with damp and hot model to establish experimentalrat foundation that contain deficiency of Yin and damp and hot . Compared the biochemisty and organizing such index as the shape , etc at the different stage of the model metioned above with those facts of MsPGN rat to find out the relationship between deficiency of Yin damp and hot and MsPGN on the development of illness and the role in MsPGN course, know the disease machine of MsPGN and treat MsPGN for Chinese medicine, screen the effective square medicine and establish the experiment foundation.

实验研究本实验采用改良的慢性血清病MsPGN动物模型,将其与具有一定实验研究基础的大鼠阴虚,湿热证模型有机结合起来,建立大鼠实验性MsPGN阴虚湿热蕴结证的病证结合模型,通过与单纯实验性大鼠MsPGN模型不同造模阶段的生化、组织形态等指标的比较,探讨阴虚湿热蕴结与MsPGN发病的关系及其在MsPGN发病过程中的作用,为中医认识MsPGN的病机及治疗MsPGN,筛选有效方药奠定理论基础。

This paper mainly aims at analysis of gastrointestinal mucosa gene expression profiles of paired samples about spleen deficiency of chronic superficial gastritis and normal people group, and spleen deficiency of chronic superficial gastritis and piwei damp-heat group. 9 and 12 different genes are selected by using Wilcoxon signed rank test, the ratio of quadratic sum between groups and within groups and distance-related analysis in the process of feature selection.

通过对慢性浅表性胃炎脾虚证与正常人、慢性浅表性胃炎脾虚证与脾胃湿热证两组胃肠粘膜配对样本的基因表达谱进行分析,在特征提取阶段分别利用Wilcoxon符号秩检验、组间和组内平方和比率、基于相关距离的冗余分析方法,分别得到9个和12个差异基因。

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