muscular相关论文
目的:汇总分析文献报道的室间隔肌部瘤(MuVSA)的临床特点与诊治情况。方法:从中国生物医学文献数据库(CBM)、中国知识资源总库(CCNKI,中......
BACKGROUND Patients with Becker muscular dystrophy(BMD)have a high risk of developing hyperkalemia,rhabdomyolysis,and ma......
Spinal muscular atrophy is an autosomal recessive neuromuscular disease with incidence of 1 in 5000 to 10000 live births......
Alpha-dystroglycanopathy(α-DGP)is a subtype of congenital muscular dystrophies(CMDs)with autosomal recessive inheritanc......
Catalpol counteracts the pathology in a mouse model of Duchenne muscular dystrophy by inhibiting the
Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disease caused by a mutation in the gene encoding the d......
Homozygous deletion, c. 1114-1116del, in exon 8 of the CRPPA gene causes congenital muscular dystrop
BACKGROUND Congenital muscular dystrophy(CMD)is a clinically and genetically heterogeneous group of inherited muscle dis......
Muscular atrophy and weakness in the lower extremities in Behçet’s disease: A case report and review
BACKGROUND In Behçet’s disease(BD),very few cases of muscular involvement have been reported previously.The natural hi......
AIM: To determine the incidence of appendiceal Crohn’s disease(CD) and to summarize the characteristic histologic featu......
Duchenne 肌肉发达的营养障碍(DMD ) 是为青春和孩子的致命的基因疾病。DMD 病人的 8 活体检视被决定并且证明膜绑定氮的氧化物 sy......
遗传性脊髓近端肌萎缩症(Hereditary proximal spinal muscular atrophy)是一种少见的神经肌肉系统遗传性疾病。发病年龄多在1~17......
假性肥大型进行性肌营养不良(Duchenne muscular dystrophy,简称DMD)为X连锁隐性遗传,男性患病,女
Duchenne muscular dystrophy......
Duchenne型肌营养不良症(Duchenne muscular dustrophy)简称DMD,是一种遗传性疾病,其特征主要是骨盆与肩带肌无力,萎缩,而腓肠肌......
进行性肌营养不良症(Progressive muscular dystrophy,PMD)是一组原发于肌肉组织的遗传性变性疾病,为进一步总结其临床特征,将我......
背景:国内外已有实验动物和临床应用脐血间充质干细胞移植治疗神经系统遗传性疾病安全、有效的诸多报道。目的:探讨脐血间充质干细......
目的 探讨杜氏肌营养不良症 (Duchenne muscular dystrophy,DMD)的无创性产前基因诊断的可行性。方法 用不连续密度梯度离心方法......
The aim of the study was to investigate the functional performance in children with spina bifida, using the Pediatric Ev......
Myotonic dystrophy type 1(DM1) is multisystem disease arising from mutant CTG expansion in the nontranslating region of ......
Rapid genetic diagnosis and prenatal diagnosis of spinal muscular atrophy by denaturing high-perform
Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disorder (1 in 6000 to 10 000 births) caused......
Background Spinal muscular atrophy (SMA) is an autosomal recessive disease characterized by degeneration of anterior hor......
Although Chen Chunyu, the head of our tour group had told us to get ready by eight o’clock, XiuXiu and ......
Endometriosis is a common benign disease affectingabout 10% to 20% of women.The frequency ofintestinal endometriosis va......
Adenomyomatosis of the gallbladder in childhood: A systematic review of the literature and an additi
AIM: To investigate the diagnostic and therapeutic assessment in children with adenomyomatosis of the gallbladder(AMG).M......
Objective To report one case of neuroleptic malignant syndrome (NMS) with raising blood sugar. Methods The patient was s......
AIM To correlate the Pang and Lee class with the clinical course in a consecutive series of patients presenting with pai......
AIM To investigate different etiologies and management of the rhabdomyolysis in children.METHODS Eight pediatric rhabdom......
很多人体质指数“专业上”超重,实际上却健康苗条。如果你也是其中的一员的话,那么下面的这则报道会让你觉得很中听。一种新的测试......
Transforming Growth Factor-β1 Induces Transdifferentiation of Fibroblasts into Myofibroblasts in Hyp
The muscularization of non-muscular pulmonary arterioles is an important pathological featureof hypoxic pulmonary vascu......
请下载后查看,本文暂不支持在线获取查看简介。
Please download to view, this article does not support online access to view......
Eteplirsen由美国Sarepta Therapeutics公司开发,用于治疗杜氏肌营养不良症(Duchenne muscular dystrophy,DMD),商品名为Exondys 5......
AIM: To evaluate the role of fluorine-18-labeled fluorodeoxyglucose positron emission tomography (18F-FDG PET) in variou......
Adeno-associated virus vectors simultaneously encoding VEGF and angiopoietin-1 enhances neovasculari
Aim:Angiopoietin-1 (Ang1) and vascular endothelial growth factor A (VEGF)play important roles in vascular formation and......
AIM:To investigate the effect of quercetin supplementation on the myenteric neurons and glia in the cecum of diabetic ra......
Tissue engineered esophagus by copper——small intestinal submucosa graft for esophageal repair in a c
Acellular porcine small intestinal submucosa(SIS)has been used for esophagoplasty with success in a canine model.However......
Two new species of Lecitrhochirium Luke, 1901 were collected in marine fishes from Xiamen, Fujian Province and Nan’ao, ......
Changes of Left Ventricular Geometry Shape and Left Ventricular Regional Function in Patients With D
Objectives To assess the left ventricle regional systolic and diastolic function,left ventricle geometry and left ventic......
AIM: To assess the presence of spinal accessory neuropathy in patients with chronic neck pain.METHODS: Patients with pai......
AIM: To evaluate the efficacy,effect of preventing cardiovascular diseases and safety of statins-fibrates combination th......
Classic polyarteritis nodosa(PAN) that targets mediumsized muscular arteries and microscopic polyangiitis(MPA),character......
He is a muscleman.他是一个肌肉猛男。肌肉猛男在美语里被称为 muscular type,muscleman 或 beefy。但如果跟一个老美说“I have......
Objective To evaluate the effects of Zhibitai(ZBT) on blood lipids and arterial elasticity in patients with high cardiov......
Conventional PCR methods combined with linkage analysis based on short tandem repeats(STRs) or Karyomapping with single ......
Graves’ disease is an autoimmune disease, which can manifest with a variety of extrathyroidal clinical syndromes like o......
INTRODUCTION. Alkaloids A and B of Cissampelos pareira which are extracted and isolated from Cissampelos pareira L. (Me......
Dear Editor:A myocardial bridge is an abnormality in which the artery is covered by a superficial membranous bridge,or a......
Objective: To explore the effect and mechanism of angiotensin Ⅱ receptor blockers-Irbesartan on occurrence of ventricul......
Becker muscular dystrophy(BMD) is an X-linked recessive disorder involving mutations of the dystrophin gene. Cardiac inv......
A novel phenolic glucoside was isolated from stem barks of Alangium plantanifolium, its structure was elucidated to be 1......