Dayna Griffiths,Jonathan Sturm
Dayna Griffiths
Introduction. Stroke in people under 45 years of age is less frequent than in older populations but has a major impact on the individual and society. In this article we provide an overview of the epidemiology and etiology of young stroke. M...
Atypical Strokes in a Young African American Male: A Case of Mitochondrial Encephalopathy Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome [0.03%]
线粒体脑肌病伴乳酸酸中毒和其他系统受累综合征(MELAS)的少见病例报告：一名年轻非洲裔美国男性患者的卒中样发作
Jully M Sanchez,Judy Ann Tan,Dimitrios Farmakiotis et al.
Jully M Sanchez et al.
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare but important cause of stroke-like symptoms which can often be missed Thambisetty and Newman 2004. We describe a case of a young ma...
Case Reports
Stroke research and treatment. 2011:2011:140630. DOI:10.4061/2011/140630 2011
Electroencephalography as a tool for assessment of brain ischemic alterations after open heart operations [0.03%]
脑电图评估开胸手术后脑缺血改变的临床价值
Elena Z Golukhova,Anna G Polunina,Natalia P Lefterova et al.
Elena Z Golukhova et al.
Cardiac surgery is commonly associated with brain ischemia. Few studies addressed brain electric activity changes after on-pump operations. Eyes closed EEG was performed in 22 patients (mean age: 45.2 ± 11.2) before and two weeks after val...
Linda N Bakken,Kathryn A Lee,Hesook Suzie Kim et al.
Linda N Bakken et al.
This study describes the pattern of day and night sleep and explores relationships between these patterns and sociodemographic and clinical factors as well as sleep environmental context and the patient's subjective sleep quality. Data from...
Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek Population [0.03%]
肿瘤坏死因子-857C＞T、TNFRSF1A36A＞G和TNFRSF1B676T＞G基因多态性与希腊人群缺血性卒中的相关性研究
Sofia Markoula,Anthoula Chatzikyriakidou,Sotirios Giannopoulos et al.
Sofia Markoula et al.
Background. The role of genetic factors in the predisposition to develop ischemic stroke has been assessed by previous studies. The main goal of the current study was to determine any possible role of TNF-857C>T,TNFRSF1A36A>G, and TNFRSF1B6...
Functional inflammatory genotypes in ischemic stroke: could we use them to predict age of onset and long-term outcome? [0.03%]
缺血性卒中功能性的炎症基因型：能否利用它们来预测发病年龄和长期预后？
Stella Marousi,Anna Antonacopoulou,Haralambos Kalofonos et al.
Stella Marousi et al.
Functional single-nucleotide polymorphisms (SNPs) of inflammatory cytokines have been previously related to the occurrence of an ischemic stroke (IS). We investigated whether five functional SNPs (i.e., TNF-α-308G>A, IL6-174G>C, IL12B 1188...
Persistent penumbra in a rabbit stroke model: incidence and histologic characteristics [0.03%]
兔卒中模型持久半影的发病率及组织学特征
Leah J Hennings,Rene Flores,Paula K Roberson et al.
Leah J Hennings et al.
Duration and extent of penumbra determine the window and brain volume in which interventions may save injured tissue after stroke. Understanding the penumbra in animals is necessary in order to design models that translate to effective clin...
Ischemic stroke in infants and children: practical management in emergency [0.03%]
儿童和婴儿的缺血性卒中：急诊处理要点
Sara Ciccone,Michela Cappella,Caterina Borgna-Pignatti
Sara Ciccone
Stroke is a rare disease in children, with an estimated incidence 13/100000 and a significant impact on morbidity and mortality. Clinical presentation and risk factors, present in almost half of pediatric patients, are not the same as in ad...
Safety and Efficacy of MLC601 in Iranian Patients after Stroke: A Double-Blind, Placebo-Controlled Clinical Trial [0.03%]
MLC601治疗卒中患者的疗效及安全性：一项随机、双盲、安慰剂对照临床试验
A A Harandi,R Abolfazli,A Hatemian et al.
A A Harandi et al.
Objective. To investigate the safety and efficacy of MLC601 (NeuroAid) as a traditional Chinese medicine on motor recovery after ischemic stroke. Methods. This study was a double-blind, placebo-controlled clinical trial on 150 patients with...
U Feldt-Rasmussen
U Feldt-Rasmussen
Fabry disease, an X-linked lysosomal storage disorder, results from deficient activity of the enzyme α-galactosidase A. Affected males with the classic phoenotype have acroparaesthesias, hypohidrosis, and corneal opacities in childhood and...