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dysplasia相关的网络例句

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与 dysplasia 相关的网络例句 [注:此内容来源于网络,仅供参考]

The following databases have been developed and are maintained by the OFA today: Hip Dysplasia, Elbow Dysplasia, Patellar Luxation, Autoimmune Thyroiditis, Congenital Cardiac Disease, Sebaceous Adenitis, Congenital Deafness, and others.

今天OFA主要发展的领域有,髋关节发育不良,肘关节发育不良,膝关节脱臼,自我免疫性甲状腺炎,先天性心脏病,脂肪性腺炎,先天性耳聋等。

OBJECTIVE: To study the effects of prolonged 75% oxygen exposure on the expression of vascular endothelial growth factor and its receptors (VEGFR1 and VEGFR2) in the neonatal rat lungs and to elucidate the effects of prolonged exposure of high concentration of oxygen on lung vascular development and its relationship with bronchopulmonary dysplasia.

目的:研究持续吸入75%氧对新生大鼠肺血管内皮生长因子(vascular endothelial growth factor,VEGF)及其受体(VEGFR1和VEGFR2)表达的影响,探讨较高浓度吸氧对肺血管发育的影响及与支气管肺发育不良(bronchopulmonary dysplasia,BPD)的关系。

Ectrodactyly, ectodermal dysplasia and clefting syndrome is characterized by split hand-split foot malformation, congenital ectodermal dysplasia and cleft lip with or without cleft palate.

目前,以先天性缺指、并指或手足裂和外胚叶发育不全伴或不伴腭裂的唇裂为主要临床表现的先天性缺指-外胚叶发育不全-唇/腭裂综合征的病因仍然不明,给疾病的防治带来了较大的困难。

Clinical manifestations are soreness on epigastric region, decreased appetite, distention after meal and eructation. It belongs to "epigastric pain" and "Stomach Pi syndrome" in TCM with characteristics of repetition and pertinacity. In 1978, WHO listed chronic atrophic gastritis as precancerous lesions of gastric cancer because its complications of intestinal metaplasia and dysplasia are closely related to gastric cancer. This has been a research focus in clinical practice and pathology for years.

临床主要表现为上腹隐痛、食欲减退、食后饱胀、嗳气等,属中医学"胃脘痛"、"胃痞"等范畴,具有反覆发作、迁延难愈的特性。1978年WHO将慢性萎缩性胃炎列为胃癌的癌前状态,而在其基础上伴发的肠上皮化生(Intestinal metaplasia,IM)和域异型增生(DYSplasia, DYS),则与胃癌的发生关系密切,被视为癌前病变(Precacerous lesions Of gastric cancer, PLGC)多年来始终是临床及病理学研究的重点。

Premature infants with bronchopulmonary dysplasia have difficulty during oral feeding because of insufficient respiratory function. Stress signs with oxygen desaturation, hyperpnea, and bradycardia are common observed during oral feeding.

罹患肺支气管发育不良(bronchopulmonary dysplasia, BPD)早产儿,因其呼吸功能障碍,经口餵食时易产生血氧饱和浓度下降、呼吸过速、心搏迟缓等压力症状。

It may be because the external ear dysplasia caused by hearing impairment, such as cochlear dysplasia, are curable by surgery; if it is caused by nerve connection, you need not worry too much pessimism and 宝宝 are still very small, in the infancy of the metabolic capacity of a strong , has many defects can be improved through its own, this is Doctor allows you to review the causes of each month.

它可能会因为外耳发育不良引起的听力障碍,比如耳蜗发育不良,是可以通过手术治愈的;如果是神经方面引起的,您也不用太悲观,宝宝还小,在婴儿时期的代谢能力很强,有很多缺陷都是可以通过自身完善的,这也是医生让您每月复查的原因。

Objective To investigate the structure and elements of deciduous teeth in a patient with cleidocranial dysplasia.

目的研究颅骨锁骨发育不良(cleidocranial dysplasia,CCD)患者乳牙牙齿结构及组分。

Paper 2:Mutation analysis of EDA gene in Chinese families with X-linked hypohidrotic ectodermal dysplasiaX-linked hypohidrotic ectodermal dysplasia(XLHED,MIM305100) is a recessive disease characterized by severe hypohidrosis,hypotrichosis and hypodontia.

论文二X连锁无汗/少汗型外胚层发育不良中EDA基因致病突变鉴定X连锁隐性无汗/少汗型外胚层发育不良(X-linked anhidrotic/hypohidroticectodermal dysplasia,XLHED;MIM305100)是无汗/少汗型外胚层发育不良(anhidrotic/hypohidrotic ectodermal dysplasia,EDA)中最常见的一种,约占95%。

We studied the mutation of PDS gene in children diagnosed to have prelingual non-syndromic hearing loss with concomitant bilateral large vestibular aqueduct and Mondini's dysplasia. We tried to find the correlation between non-syndromic hearing loss in local patients and PDS gene, and to establish the basic data of PDS gene mutations in Taiwan.

本篇研究之目的,乃对於患有非症候群学语前听障并合并双侧大前庭导水管及Mondini氏发育异常(Mondini's dysplasia)的儿童,作基因的分析,尝试找出本土非症候群听障与PDS基因的关连性,以建立台湾地区PDS基因突变的基本资料。

Background:Developmental dysplasia of hip is a frequent disease of skeletal muscular system in infant.There is about 1% to 10% infants to be prone to developmental dysplasia,dislocation,and semiluxation of hip in the borning.

研究背景及目的:发育性髋关节异常(developmental dysplasia ofhip,DDH)是婴幼儿骨骼系统最常见的疾病之一,约1%~10%的新生儿出生时有髋关节发育不良、脱位及半脱位倾向。

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