1)SCN4A正常血钾性周期麻痹
1.Objective The present study is to observe in vitro the proliferation ability of the muscle cells from permanent myopathy (PM) patients of nomokalaemic periodic paralysis (normKPP),which is caused by mutations of Met1592Val in the skeletal muscle voltage gated sodium channel (SCN4A) gene on chromosome 17q23.目的正常血钾性周期麻痹是由位于17号染色体上编码人类骨骼肌钠通道基因(SCN4A)发生突变所致,以肢体无力短暂、反复发作并完全恢复为特点,部分患者可发展为永久性肌病(permanent myopathy,PM),该病的发病机制尚不清楚,至今也无有效的治疗方法。
2)normokalemic periodic paralysis正常血钾型周期性麻痹
1.The mutation V781I in SCN4A gene exists in Chinese patients with normokalemic periodic paralysis;正常血钾型周期性麻痹存在SCN4A基因V781I突变
英文短句/例句
1.Fuctional Expression of a Novel Mutation R675Q Identified in a Chinese Normakalemic Periodic Paralysis Family;正常血钾型周期性麻痹SCN4A基因新突变R675Q的功能研究
2.Clinical Analyze on Abnormal Serum Ceatinase for Patients with Idiopathic Hypo kalemic Periodic Paralysis原发性低钾型周期性麻痹患者血清肌酶学异常的临床分析
3.Investigation and analysis of Dongguan region with hypoka lemic periodic paralysis and its nursing新莞人低钾型周期性麻痹的调查分析及护理
4.The gene alteration of hypokalemic periodic paralysis低钾型周期性麻痹一家系相关基因分析
5.CACNA1S Gene and Low-potassium Periodic ParalysisCACNA1S基因与低钾周期性麻痹
6.Genetic Research of Ion Channel Gene Mutations and Clinical Study on Primary Hypokalemic Periodic Paralysis;原发性低钾型周期性麻痹的离子通道基因突变及临床研究
7.cyclic oculomotor paralysis周期性动眼神经麻痹
8.The research progress on thyrotoxic hypokalemic periodic paralysis caused by CACNA1S genetic polymorphismCACNA1S基因多态性引起甲状腺毒性低钾周期性麻痹的研究进展
9.Clinical Observation on the Effect of Acupuncture plus Blood-letting with Three-edged Needle on 50 Patients with Bell's Palsy in the Acute Stage针刺配合三棱针放血治疗风热型Bell麻痹急性期50例临床观察
10.The effects of acut peripheral facial paralysis by physical therapy物理治疗急性期周围性面神经麻痹的疗效观察
11.Genetic Research of Disease-related Mutations and Clinical Study on Periodic Paralyses;周期性麻痹的临床及相关基因突变研究
12.Efficacy Analysis of ~(131)I in Treatment of Hyperthyroidism with Periodic Paralysis~(131)I治疗甲亢合并周期性麻痹疗效初步分析
13.The Cyclic Expression of Calcium-activated Potassium Channels in Human Endometrium;钙离子激活钾离子通道各蛋白亚型在人正常子宫内膜中的周期性表达
14.Violent model: Cent period, prodromal stage, excitement period and paralytic period.狂暴型：分三期，前驱期、兴奋期和麻痹期。
15.The Clinical Observation on the Treatment of Acute Peripheral Facial Paralysis by "Jing Jin" Acupuncture Method“经筋刺法”治疗急性期周围性面神经麻痹的临床观察
16.Clinical observation on therapeutic effect of different acupuncture therapies on acute peripheral facial paralysis周围性面神经麻痹急性期不同针灸方法疗效观察
17.Effect of Meridional Muscle Region Puncture on the Blink Reflex in Acute Infranuclear Facial Palsy经筋刺法对急性期周围性面神经麻痹患者瞬目反射的影响
18.A case of severe hypokaliemic paralysis treated by high concentration and large dose of potassium solution高浓度大剂量补钾治疗严重低钾性麻痹一例报告
相关短句/例句
normokalemic periodic paralysis正常血钾型周期性麻痹
1.The mutation V781I in SCN4A gene exists in Chinese patients with normokalemic periodic paralysis;正常血钾型周期性麻痹存在SCN4A基因V781I突变
3)normoKPP正常血钾周期性麻痹
1.We recruited a normoKPP family in Hubei China and evaluated genetic variations responsible for the disease.我们对一个来自湖北省的正常血钾周期性麻痹家系进行致病基因突变检测。
4)hypokalemic periodic paralysis低血钾型周期性麻痹
1.Results Six cases of FPP were diagnosed as hypokalemic periodic paralysis,and all occured as an autosomal do.结果6例为家族性低血钾型周期性麻痹,具有常染色体显性遗传的特征;发作时血清钾1。
5)Hypokalemic periodic paralysis低钾性周期性麻痹
1.Hypokalemic periodic paralysis: report of a Chinese pedigree with a novel mutation site in SCN4A gene;目的 通过检测相关基因的突变位点来研究低钾性周期性麻痹 (HOKPP)这一常染色体显性遗传疾病的遗传学病因。
6)Hypokalemic periodic paralysis低钾型周期性麻痹
1.Objective To find if the mutations that had been reported abroad exist in a patient with hypokalemic periodic paralysis.目的探讨低钾型周期性麻痹患者是否存在相关基因的突变。
2.Object: Hypokalemic periodic paralysis has gene disorders in chromosomes.目的:低钾型周期性麻痹为一种常染色体发生基因突变的疾病,可以是由遗传获得性的突变基因,少数病例也可以是因受孕时生殖细胞发生基因突变而产生。
延伸阅读
正常1.符合一般规律和情况。
