查询词典 syndrome

Objective To explore the clinical signifinance of CD55 and CD59 expression in diagnosis aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome.

目的研究CD55、CD59在再生障碍性贫血-阵发性睡眠性血红蛋白尿综合征中的诊断价值。

Objective To investigate the expression of membrane associated complement regulatory proteins——CD55 and CD59 on the peripheral blood cells in patients with paroxysmal nocturnal hemoglobinuria,aplastic anemia and myelodysplastic syndrome and its clinical implications.

目的 观察糖化磷脂酰肌醇（GPI连接的补体调节蛋白——CD55和CD59在阵发性睡眠性血红蛋白尿症（PNH 、再生障碍性贫血和骨髓增生异常综合征患者的外周血血细胞表达的变化并分析其在上述疾病中的临床意义。

Objective: To study the early laboratory diagnosis of hemorrhagic fever with renal syndrome.

目的：探讨肾综合征出血热患者的早期实验室诊断。

Heiner's syndrome consists of pulmonary hemosiderosis associated with allergic reactions after ingesting cow's milk. Pulmonary hemosiderosis is characterized by the accumulation of iron within the pulmonary macrophages as hemosiderin combined with iron-deficiency anemia.

海纳氏症候群是指对牛奶蛋白过敏合并肺血铁质沉积症的病人，而肺血铁质沉积症是指在肺部有不正常的血铁质沉积在肺部的巨噬细胞，在x光上有肺部侵润并且因血铁质沉积而造成缺铁性贫血。

among type 2 diabetes chimese medical pattern of syndrome , phlegmatic hygrosis , meridian and vessels and deficiency of both yin and yang s' blood sugar are not well controlled , metabolic disorder is severe , so there are many patients who have hepatica .

阴阳两虚型和气阴两虚型有共同的脂代谢情况：两者的脂代谢紊乱都以TC和HDL的代谢紊乱为主，表现为TC的明显升高和HDL的明显降低。

PURPOSE : Pass studying type 2 diabetes chinese medical science' pattern of syndrome together with relation of metabolic disorder and hepatica ,providing leading effect for chian and west medcine to cure diabetes afterward.

目的：观察2型糖尿病中医证型与脂代谢紊乱、并发脂肪肝的关系。为中西医结合防治2型糖尿病脂代谢紊乱和并发脂肪肝提供理论和临床依据。

ABSTRACT］ Objective To explore the characteristics of traditional Chinese medical syndrome of hepatocirrhosis.

摘要］ 目的探讨肝炎后肝硬化中医证候特点。

Background— Primary ciliary dyskinesia is a recessie genetic disorder that is characterized by sinopulmonary disease and reflects abnormal ciliary structure and function. Situs inersus totalis occurs in 50% of PCD patients (Kartagener's syndrome in PCD), and there are a few reports of PCD with heterotaxy, such as cardioascular anomalies.

背景 先天性纤毛运动异常症是以呼吸道感染和纤毛结构与功能不正常为特征的隐性遗传性疾病。50% PCD患者易发生完全性内脏异位(如PCD中的Kartagener综合征)，有小部分PCD伴有心脏旋转不良等心血管异常现象。

Situs inersus totalis occurs in 50% of PCD patients (Kartagener's syndrome in PCD), and there are a few reports of PCD with heterotaxy, such as cardioascular anomalies.

完全性内脏逆位在50%原发性纤毛运动障碍患者中出现。有少数病例报道原发性纤毛运动障碍伴有内脏逆位，比如心血管畸形。

Their ages ranged 6 to 13 years. Their EEGs were characterized by continuous spike-and-wave discharges during non-rapid eye movement sleep, accounting for 85%-100% of the period of NREM sleep. Clinically, these children had various types of epileptic seizures and exhibited different degrees of neuropsychiatric impairments, language dysfunction, and/or behavioral disturbances. Neuroimaging abnormalities were found in 6 cases, including atelencephalia or atrophy, gray matter heterotopia and leucomalacia. CONCLUSIONS: This study indicates the characteristics of CSWS syndrome in clinical manifestations, EEG and neuroimaging examinations.

结果：9例患儿的视频脑电图结果符合CSWS诊断标准，年龄6~13岁，脑电图表现为棘慢复合波在整个非快速眼动睡眠期几乎持续存在，其放电时间占整个NREM期的85%~100%；临床上患者表现不同类型的癫癎发作，在神经精神方面存在不同程度的损害，存在言语和/或行为障碍；其中6例患儿显示有神经影像学异常，包括脑发育不全或萎缩、灰质异位、脑白质软化等。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。