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Mild diarrhea leading to tacrolimus toxicity in an immunocompromised patient with suspected community-acquired pneumonia:a case report
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作者 Xueying Chen Jianbo Ding +3 位作者 Jiali Zhang Hongyan Jiang Haibin Dai Lingyan Yu 《World Journal of Emergency Medicine》 2025年第2期174-176,共3页
Tacrolimus (TAC) is increasingly used for immunosuppression in organ transplantation,dermatomyositis/polymyositis,and myasthenia gravis(MG) patients.^([1]) TAC has a narrow therapeutic window with overexposure leading... Tacrolimus (TAC) is increasingly used for immunosuppression in organ transplantation,dermatomyositis/polymyositis,and myasthenia gravis(MG) patients.^([1]) TAC has a narrow therapeutic window with overexposure leading to acute and chronic forms of adverse reactions (ADRs).After oral administration,TAC is predominantly absorbed in the duodenum and jejunum and has highly variable pharmacokinetics,particularly when diarrhea occurs.^([2,3]) Few data has been published on TAC overexposure following mild diarrhea.Mild diarrhea is relatively common and often unreported,which can easily be overlooked by physicians,especially in the emergency department.Here,we report the occurrence of serious ADRs to TAC after mild diarrhea in a MG patient with community-acquired pneumonia(CAP),including nephrotoxicity,metabolic abnormalities and severe immunosuppression. 展开更多
关键词 DIARRHEA PNEUMONIA GRAVIS
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重症肌无力患儿,告别难“咽”之苦
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作者 梁薇 黄秋艳 +1 位作者 李小晶 沈慧玲 《健康养生》 2025年第14期40-41,共2页
重症肌无力(Myasthenia Gravis,MG)是一种自身免疫性疾病,主要影响神经与肌肉之间的信号传递。患者的免疫系统错误地攻击了神经肌肉接头处的乙酰胆碱受体,导致部分或全身骨骼肌肌肉无力和疲劳。根据受累肌肉的不同,重症肌无力的症状表... 重症肌无力(Myasthenia Gravis,MG)是一种自身免疫性疾病,主要影响神经与肌肉之间的信号传递。患者的免疫系统错误地攻击了神经肌肉接头处的乙酰胆碱受体,导致部分或全身骨骼肌肌肉无力和疲劳。根据受累肌肉的不同,重症肌无力的症状表现多样,包括眼睑下垂、面部肌肉无力、吞咽障碍、四肢乏力等,且常常呈现出“晨轻暮重”的波动特点。 展开更多
关键词 重症肌无力 Myasthenia Gravis 乙酰胆碱受体
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THE GRAVY TRAIN
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作者 LAN XINZHEN 《Beijing Review》 2007年第35期22-23,共2页
The Qinghai-Tibet Railway, the highest rail in the world, was hailed as a miracle of engineeringwhen it began running a year ago. Today, it isbeing hailed for the economic benefits it hasbrought to the once isolated r... The Qinghai-Tibet Railway, the highest rail in the world, was hailed as a miracle of engineeringwhen it began running a year ago. Today, it isbeing hailed for the economic benefits it hasbrought to the once isolated region of 展开更多
关键词 THE gravy TRAIN
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Interactions Between Extracellular Vesicles and Autophagy in Neuroimmune Disorders 被引量:1
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作者 Xiwen Ai Haojun Yu +1 位作者 Yu Cai Yangtai Guan 《Neuroscience Bulletin》 SCIE CAS CSCD 2024年第7期992-1006,共15页
Neuroimmune disorders,such as multiple sclerosis,neuromyelitis optica spectrum disorder,myasthenia gravis,and Guillain–Barrésyndrome,are characterized by the dysfunction of both the immune system and the nervous... Neuroimmune disorders,such as multiple sclerosis,neuromyelitis optica spectrum disorder,myasthenia gravis,and Guillain–Barrésyndrome,are characterized by the dysfunction of both the immune system and the nervous system.Increasing evidence suggests that extracellular vesicles and autophagy are closely associated with the pathogenesis of these disorders.In this review,we summarize the current understanding of the interactions between extracellular vesicles and autophagy in neuroimmune disorders and discuss their potential diagnostic and therapeutic applications.Here we highlight the need for further research to fully understand the mechanisms underlying these disorders,and to develop new diagnostic and therapeutic strategies. 展开更多
关键词 AUTOPHAGY Extracellular vesicles Neuroimmune disorders Multiple sclerosis Neuromyelitis optica spectrum disorder Myasthenia gravis Guillain-Barrésyndrome
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Perioperative cardiac risks in myasthenia gravis 被引量:1
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作者 Deb Sanjay Nag Abhishek Chatterjee +2 位作者 Pratap Rudra Mahanty Merina Sam Murari Kumar Bharadwaj 《World Journal of Clinical Cases》 SCIE 2024年第13期2147-2150,共4页
Myasthenia gravis(MG)is an autoimmune disorder that affects the neuromuscular junction.The primary pathology in MG involves the presence of autoantibodies to acetylcholine receptors(AChRs),which results in qualitative... Myasthenia gravis(MG)is an autoimmune disorder that affects the neuromuscular junction.The primary pathology in MG involves the presence of autoantibodies to acetylcholine receptors(AChRs),which results in qualitative and quantitative reductions in the availability of functional AChRs.Cardiac muscles are also affected,resulting in various perioperative cardiac complications.Antistriational antibodies are commonly reported in MG cases with cardiac involvement.In the presence of thymoma,the prevalence of cardiac manifestations in patients with MG increases to approximately 10%-15%.Cardiac involvement in MG may range from asymptomatic electrocardiogram changes to ventricular tachycardia,myocarditis,conduction disorders,heart failure,and sudden death.Increased incidence of atrial fibrillation,ventricular and supraventricular extra systoles,and prolonged QTc have also been reported in patients with MG.Clinicians should consider the evaluation of autonomic dysfunction and risk of cardiovascular disease in patients with MG. 展开更多
关键词 Myasthenia Gravis Perioperative period RECEPTORS CHOLINERGIC ANESTHESIA
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Cardiac implications in myasthenia gravis
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作者 Praveen Reddy Elmati Gowthami Sai Kogilathota Jagirdhar Salim Surani 《World Journal of Clinical Cases》 SCIE 2024年第26期5863-5867,共5页
This editorial aimed to consolidate the current evidence in literature on the association between myasthenia gravis(MG)and cardiac involvement,focusing on the impact of thymoma,antistriational antibodies,and late-onse... This editorial aimed to consolidate the current evidence in literature on the association between myasthenia gravis(MG)and cardiac involvement,focusing on the impact of thymoma,antistriational antibodies,and late-onset MG.Additionally,the study aimed to explore the influence of genetic differences among populations on the association with cardiac disease.We conducted a review of existing literature in PubMed and Google Scholar to find relevant studies on cardiac involvement in MG.We created search criteria using a combination of free text words,including MG,antistriational antibodies,thymectomy,cardiomyopathy,myocarditis,arrhythmias,autonomic dysfunction.Relevant articles published in English language were analyzed and incorporated.The findings indicate a strong association between thymoma,myasthenic crisis,antistriational antibodies,and late-onset MG with cardiac involvement.The study also revealed that genetic differences among populations influence the risk of cardiac disease and electrocardiography(ECG)abnormalities in MG patients.Autonomic dysfunctions altered cardiac autonomic response and increased susceptibility to arrhythmias and sudden cardiac death in MG patients.The study supports the significance of thymoma,antistriational antibodies,and late-onset MG as key factors associated with cardiac involvement in MG patients.It emphasizes the importance of ECG as the initial test in managing MG patients,particularly in the perioperative period,to identify and genetic testing if needed to address their cardiac risk effectively. 展开更多
关键词 Myasthenia gravis Antistriational antibodies THYMECTOMY CARDIOMYOPATHY MYOCARDITIS ARRHYTHMIAS Autonomic dysfunction
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Clinical Value of Platelet-Related Parameters and Monocyte Counts in Patients with Oculomotor Myasthenia Gravis
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作者 Yaping Sun Xianglin Cheng Ke Peng 《Case Reports in Clinical Medicine》 2024年第12期572-580,共9页
Background: Our study aimed to investigate the clinical value of platelet parameters and the number of Monocytes (MONO) in the peripheral blood of patients with Ocular Myasthenia Gravis (OMG). Methods: Fifty patients ... Background: Our study aimed to investigate the clinical value of platelet parameters and the number of Monocytes (MONO) in the peripheral blood of patients with Ocular Myasthenia Gravis (OMG). Methods: Fifty patients discharged from the Department of Neurology of the First People’s Hospital of Jingzhou City with the diagnosis of OMG from January 1, 2020, to December 31, 2023, were selected as the experimental group, and healthy medical examiners were selected as the control group during the same period. The differences in peripheral blood mononuclear cell count and platelet-related parameters between the two groups were compared. ROC curves were drawn to analyze the clinical value of the studied indexes in patients with OMG. Results: Patients with OMG had significantly higher monocyte counts and narrower platelet distributions compared with normal adults;further logistic regression analysis revealed that higher monocyte counts and narrower Platelet Distribution Width (PDW) may be independent influences on the occurrence of OMG (p Conclusion: Peripheral blood mononuclear cell count and PDW have some diagnostic value in OMG. 展开更多
关键词 Ocular Myasthenia Gravis Mononuclear Cell Platelet Distribution Width
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重症肌无力的临床研究现状 被引量:11
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作者 王丽芳 毛梅 +2 位作者 张宇(综述) 邓晖 冯加纯(审校) 《中风与神经疾病杂志》 CAS 北大核心 2016年第1期82-85,共4页
重症肌无力(myasthenia gravis,MG)是一种神经肌肉接头传递障碍的自身免疫性疾病,其病变部位在突触后膜,主要表现为骨骼肌易疲劳。除了我们熟知的症状,MG患者还会出现不安腿综合征(restless legs syndrome,RLS)、睡眠障碍性呼吸(sl... 重症肌无力(myasthenia gravis,MG)是一种神经肌肉接头传递障碍的自身免疫性疾病,其病变部位在突触后膜,主要表现为骨骼肌易疲劳。除了我们熟知的症状,MG患者还会出现不安腿综合征(restless legs syndrome,RLS)、睡眠障碍性呼吸(sleep-disordered breathing,SDB)及嗅觉、听觉、认知等非运动症状。MG自身免疫性抗体是目前临床研究的热点,MG的临床分型也倾向于与不同抗体类型有关。 展开更多
关键词 重症肌无力 运动症状 自身免疫性抗体 MYASTHENIA GRAVIS 自身免疫性疾病 睡眠障碍性呼吸 ACHR 不安腿综合征 突触后膜
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Sixty cases of ocular myasthenia gravis treated with acupuncture and moxibustion at extra-meridian and collateral 被引量:3
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作者 陈金亮 潘朝 +1 位作者 刘艳君 LIU Zhao 《World Journal of Acupuncture-Moxibustion》 2012年第4期56-59,共4页
Objective To explore effective therapeutic method for the treatment of ocular myasthenia gravis. Methods Sixty cases of ocular myasthenia gravis were selected. The acupuncture was applied at Dàzhuī (大椎 GV 14... Objective To explore effective therapeutic method for the treatment of ocular myasthenia gravis. Methods Sixty cases of ocular myasthenia gravis were selected. The acupuncture was applied at Dàzhuī (大椎 GV 14), Bǎihuì (百会 GV 20), Shàngxīng (上星 GV 23) of Governor Vessel, and its crossing points with Yinqiao and Yangqiao Meridian, such as Jīngmíng (睛明 BL 1), shēnmài (申脉 BL 62), Dìcāng (地仓 ST 4), Jūliáo (巨髎 ST 3), Chéngqì (承泣 ST 1 ), etc. Besides, ginger-partition moxibustion was applied at Yángbái (阳白 GB 14) and Sìbái (四白 ST 2). The plum-blossom needle was applied at upper limb distribution of lung channel of hand taiyin, heart channel of hand shaoyin and pericardium channel of hand jueyin. The patients’ clinical symptoms, potential degradation percentages of repetitive nerve stimulation (RNS) in low frequency were observed. Results 8 cases were clinically cured, 20 cases were basically cured, 12 cases were remarkably effective, 15 cases were effective and 5 cases were failed. The total effective rate was 91.7%. Compared with before the treatment, the potential degradation percentages of repetitive nerve stimulation in low frequency were lowered [(19.44±6.28)% vs (8.78±3.12)%, (P0.05)]. Conclusion Acupuncture and moxibustion at extra-meridian and collateral for ocular myasthenia gravis could achieve positive efficacy. 展开更多
关键词 ocular myasthenia gravis acupuncture therapy extra-meridian and collateral plum-blossom needle prick
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中西医结合治疗重症肌无力临床疗效和安全性的Meta分析 被引量:13
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作者 双晓萍 谭子虎 +2 位作者 陈乞 陈子薇 陈丽珠 《中国中医药科技》 CAS 2016年第1期121-124,共4页
重症肌无力(myasthenia gravis,MG)是一种自身免疫性疾病[1-2]。中医药工作者对MG展开了大量的研究工作,体现出中医药独特的优势及前景。为此,笔者全面收集中西医结合治疗MG的临床随机对照试验,进行Meta分析,以期为临床实践提供可靠... 重症肌无力(myasthenia gravis,MG)是一种自身免疫性疾病[1-2]。中医药工作者对MG展开了大量的研究工作,体现出中医药独特的优势及前景。为此,笔者全面收集中西医结合治疗MG的临床随机对照试验,进行Meta分析,以期为临床实践提供可靠依据。1资料与方法1.1文献来源中国知识资源总库(CNKI)、万方学术期刊全文数据库、维普中文期刊数据库(VIP)、中国生物医学文献服务系统(CBM)作为资料源,包括其公开发表于国内医学期刊及未发表的文献资料如学术报告、会议论文集或毕业论文等。 展开更多
关键词 重症肌无力 META分析 中西医结合 中文期刊数据库 MYASTHENIA 学术期刊全文 GRAVIS 中医药工作者 自身免疫性疾病 绝对评分
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术后放疗在胸腺瘤中的作用及研究进展 被引量:4
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作者 贾佳 李月敏 《实用医学杂志》 CAS 北大核心 2016年第15期2573-2575,共3页
胸腺瘤(thymic tumor,TT)位于前纵膈内、来源于胸腺上皮,是一种潜在恶性生长且相对惰性的罕见肿瘤,约占所有恶性肿瘤的0.2%~1.5%。常发生在40~70岁,儿童罕见约占10%。根据2004年WHO病理组织学分型,TT分为(A,AB,B1,B2和B3型)或TC... 胸腺瘤(thymic tumor,TT)位于前纵膈内、来源于胸腺上皮,是一种潜在恶性生长且相对惰性的罕见肿瘤,约占所有恶性肿瘤的0.2%~1.5%。常发生在40~70岁,儿童罕见约占10%。根据2004年WHO病理组织学分型,TT分为(A,AB,B1,B2和B3型)或TC(已被单列)。目前Masaoka-Koga分期为TT的最新分期,但临床上仍以Masaoka分期(Ⅰ~Ⅳ期)为标准。 展开更多
关键词 胸腺瘤 术后放疗 组织学分型 纵膈 腺上皮 肌无力危象 MYASTHENIA 重症肌无力 GRAVIS 重离子
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调节性T细胞和辅助性T细胞17细胞失衡在重症肌无力中的研究进展 被引量:4
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作者 陈渊 张鹏 《实用医学杂志》 CAS 北大核心 2016年第15期2578-2580,共3页
重症肌无力(myasthenia gravis,MG)是自身抗体直接作用于神经肌肉街头引起的以肌肉无力为临床特征的一种自身免疫性疾病。主要的抗原靶点为乙酰胆碱受体(acetylcholine receptor,ACh R),其次为肌肉特异性激酶(muscle-specific kina... 重症肌无力(myasthenia gravis,MG)是自身抗体直接作用于神经肌肉街头引起的以肌肉无力为临床特征的一种自身免疫性疾病。主要的抗原靶点为乙酰胆碱受体(acetylcholine receptor,ACh R),其次为肌肉特异性激酶(muscle-specific kinase,Mu SK)和低密度脂蛋白受体相关蛋白4(low density lipoprotein receptor-related protein 4,LRP4)。 展开更多
关键词 重症肌无力 自身免疫性疾病 MYASTHENIA 神经肌肉 GRAVIS 乙酰胆碱受体 胸腺组织 自身抗体 免疫调节 细胞分化
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硫唑嘌呤治疗晚发型重症肌无力的疗效 被引量:2
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作者 李平 李双英 张巧莲 《实用医学杂志》 CAS 北大核心 2016年第10期1725-1726,共2页
重症肌无力(myasthenia gravis)是一种获得性自身免疫性疾病,一般认为发病年龄有2个高峰,分为早发型和晚发型。但近年临床资料显示,晚发型重症肌无力(late-onset myasthenia gravis,LOMG)的发病呈增高趋势。
关键词 重症肌无力 晚发型 MYASTHENIA GRAVIS 硫唑嘌呤 自身免疫性疾病 发病年龄 新斯的明试验 四肢肌肉 糖皮质激素
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Histologic Classification of Thymoma and Its Relationship with Myasthenia Gravis and Clinical Stages of the Tumor 被引量:1
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作者 王新允 陈云新 +1 位作者 王爱香 张淑敏 《The Chinese-German Journal of Clinical Oncology》 CAS 2005年第5期314-316,327,共4页
Objective: To investigate the relationship among the latest WHO classification of thymoma, myasthenia gravis (MG) and clinical stages. Methods: To review the pathological sections of 74 patients with thymoma from ... Objective: To investigate the relationship among the latest WHO classification of thymoma, myasthenia gravis (MG) and clinical stages. Methods: To review the pathological sections of 74 patients with thymoma from 1980-2004 using WHO classification (1999), the statistical software was used to analyze the relationship among the WHO classification, MG and clinical stages. Results: (1) Two cases of type A, 23 cases of type AB, 4 cases of type B1, 27 cases of type B2, 16 cases of type B3 and 2 cases of type C were classified. Type B2 more likely accompanied MG (P〈0.05), while none with MG occurred for type C. (2) One patient was in stage Ⅰ, 30 were in stage Ⅱ, 38 were in stage Ⅲ, and 5 were in stage Ⅳ. The latest histologic classification was significantly correlated with Masaoka stages (P〈0.01). Conclusion: The latest WHO classification was correlated with occurrence of MG and finely reflected clinical stage. It can also evaluate the prognosis of patients. 展开更多
关键词 THYMOMA myasthenia gravis clinical stages
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重症肌无力的治疗进展 被引量:1
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作者 于磊 徐严明 徐萍蓉 《华西医学》 CAS 2008年第6期1510-1511,共2页
关键词 重症肌无力 胸腺切除术 ACHR 乙酰胆碱受体 血浆交换 MYASTHENIA GRAVIS 眼肌型 自身免疫性疾病 胸腺组织
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重症肌无力相关抗体及与胸腺疾病相关性的研究进展 被引量:1
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作者 张哲峰 金凤 薛雷 《中风与神经疾病杂志》 CAS 北大核心 2015年第10期957-958,共2页
重症肌无力(myathenia gravis,MG)是由T细胞辅助、抗体介导并有补体参与的一种神经-肌肉接头传递功能障碍的获得性自身免疫性疾病。它是神经肌肉传导疾病中较为常见的疾病,患者可表现为波动性的肌无力,易疲劳和晨轻暮重症状。在绝大... 重症肌无力(myathenia gravis,MG)是由T细胞辅助、抗体介导并有补体参与的一种神经-肌肉接头传递功能障碍的获得性自身免疫性疾病。它是神经肌肉传导疾病中较为常见的疾病,患者可表现为波动性的肌无力,易疲劳和晨轻暮重症状。在绝大多数情况下,骨骼肌乙酰胆碱受体(AChR)成为自身免疫攻击靶点,然而也存在其它的攻击靶点比如肌肉特异性受体酪氨酸激酶(Mu SK)。 展开更多
关键词 重症肌无力 攻击靶点 胸腺疾病 自身免疫性疾病 ACHR 神经肌肉 乙酰胆碱受体 胸腺瘤 GRAVIS 神经-肌肉接头
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儿童重症肌无力合并桥本甲状腺炎1例报道 被引量:1
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作者 杨均 李作孝 《重庆医学》 CAS 北大核心 2015年第21期3023-3024,共2页
重症肌无力(myasthenia gravis,MG)是神经肌肉接头疾病中常见的一种,各个年龄阶段均可发病,儿童患者合并桥本甲状腺炎(Hashimoto′s thyroiditis,HT)临床上较少见。1临床资料患者,女,10岁,患者于3个月前无明显原因出现视物成双,向... 重症肌无力(myasthenia gravis,MG)是神经肌肉接头疾病中常见的一种,各个年龄阶段均可发病,儿童患者合并桥本甲状腺炎(Hashimoto′s thyroiditis,HT)临床上较少见。1临床资料患者,女,10岁,患者于3个月前无明显原因出现视物成双,向左注视时明显,并进行性加重。2个月前出现右侧眼睑下垂,伴晨轻暮重,被动睁眼时伴有视物成双。 展开更多
关键词 儿童重症肌无力 桥本甲状腺炎 视物成双 MYASTHENIA GRAVIS 神经肌肉接头 THYROIDITIS 新斯的明试验 晨轻暮重 胸腺切除术
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ANCA阳性的重症肌无力合并桥本甲状腺炎、周围性面瘫1例 被引量:1
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作者 关文娟 王天舒 +2 位作者 景黎君 滕军放 贾延劼 《国际神经病学神经外科学杂志》 2014年第6期529-530,共2页
重症肌无力(myasthenia gravis,MG)是神经内科常见的自身免疫性疾病,以受累肌肉的无力、易疲劳为主要表现,可以合并Graves病、桥本甲状腺炎、系统性红斑狼疮、吉兰-巴雷综合征等多种自身免疫性疾病。但到目前为止,国内尚无MG合并桥本... 重症肌无力(myasthenia gravis,MG)是神经内科常见的自身免疫性疾病,以受累肌肉的无力、易疲劳为主要表现,可以合并Graves病、桥本甲状腺炎、系统性红斑狼疮、吉兰-巴雷综合征等多种自身免疫性疾病。但到目前为止,国内尚无MG合并桥本甲状腺炎(Hashimoto’s thyroiditis,HT),同时又合并ANCA阳性和周围性面瘫的报道。本文就新近收治的一例合并多种抗体阳性的MG患者进行分析,旨在提高对本病的进一步认识。 展开更多
关键词 ANCA阳性 桥本甲状腺炎 重症肌无力 周围性面瘫 自身免疫性疾病 MYASTHENIA GRAVIS thyroiditis 系统性红斑狼疮 新斯的明试验
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Identification and Physiochemical Analysis of ERK Interacting Proteins Using Bio-Computational Tools 被引量:1
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作者 Khuleshwari Kurrey Vijay Paramanik 《World Journal of Neuroscience》 2018年第2期303-313,共11页
ERK (Extracellular Signal Regulated Kinase) or MAP kinase is an intracellular signaling molecule. ERK is involved in regulation of various functions i.e. cell proliferation, cell migrations, cell survival and many mor... ERK (Extracellular Signal Regulated Kinase) or MAP kinase is an intracellular signaling molecule. ERK is involved in regulation of various functions i.e. cell proliferation, cell migrations, cell survival and many more. It gets activated in response of various stimuli like growth factors, cytokines, virus, second messengers, transforming agents and carcinogens. While transferring signals from cell surface receptors to cell nucleus, ERK interacts with a numbers of proteins. Physiochemical and functional characterization of these proteins is little known. Thus, we attempted to study physiochemical and functional properties of ERK interacting proteins using bio-computational tools. ExPASy and SOSUI server suggested 22 ERK interacting proteins. Physical and chemical parameters of these ERK interacting partners indicated higher percentage of hydrophobic amino acid and leucine as major constituent. Moreover, the instability index indicated that four proteins are stable in over wide range temperature in vitro, and remaining eighteen proteins were found unstable. In addition, SOSUI server showed that fifteen proteins were soluble and six are trans-membrane in nature. 展开更多
关键词 EXTRACELLULAR SIGNAL Regulated KINASE (ERK) gravy SOSUI STRING STITCH ExPASy
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Th17在重症肌无力发病机制中作用的研究进展
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作者 金迪 李颖 付锦 《中国免疫学杂志》 CAS CSCD 北大核心 2014年第9期1272-1274,共3页
重症肌无力(Myasthenia gravis,MG)是一种神经肌肉接头传递障碍的获得性自身免疫性疾病。病变主要累及神经-肌肉接头突触后膜上乙酰胆碱受体(Acetylcholine receptor,AChR),临床特征为部分或全身骨骼肌极易疲劳,晨轻暮重,休息和胆... 重症肌无力(Myasthenia gravis,MG)是一种神经肌肉接头传递障碍的获得性自身免疫性疾病。病变主要累及神经-肌肉接头突触后膜上乙酰胆碱受体(Acetylcholine receptor,AChR),临床特征为部分或全身骨骼肌极易疲劳,晨轻暮重,休息和胆碱酯酶抑制剂治疗后有效。 展开更多
关键词 重症肌无力 TH17 ACHR 乙酰胆碱受体 GRAVIS 神经-肌肉接头 突触后膜 自身免疫性疾病 全身骨骼肌 晨轻暮重
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