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医学杂志帮忙投稿

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医学杂志帮忙投稿

据学术堂了解,想要成功、快速的发表论文,提前了解期刊杂志的审核流程很重要,可以帮助大家及时掌握投稿进度,提高效率:

流程一:

投稿——初审——通过——通知——汇款——定版——出刊——邮递

流程二:

投稿——初审——修改——不通过

1、投稿:主要接收邮箱投稿和在线投稿系统投稿

2、初审:投稿文章三个工作日内给安排审核,并出审核结果

3、通过:对于审核通过的文章尽快作出用稿答复

4、不通过:审核不通过的文章会通知作者不通过的原因,并提出修改意见

5、通知:通知通常为邮件形式。如需书面的,尽快给予安排邮递

6、汇款:办理文章发表相关费用,提供公司账户,法人账户,邮局地址汇款3种方式 定版:确认款到的,及时安排文章定版

7、出刊:杂志社定时排版,印刷,出刊。大部分期刊会定期出刊,也有部分会根据自身情况选择提前或退后出刊。通常提前和退后时间不超过1个月

8、邮递:对于所有的发表作者,我们都会安排邮递当期杂志1本或2本。

医学论文发表注意事项:

1、正确选择期刊杂志:

选择期刊时,除了要考虑期刊杂志的正规性以外,还要考虑期刊的类别,医学期刊有专业性期刊和综合性期刊两大类,应同时考虑,不要只向专业性期刊投稿,无形中缩窄了论文发表的渠道

2、了解拟投期刊的外部特征

每种期刊都有自己详细的稿约,一般刊登在每年的最后一期或第一期。投稿前,应仔细阅读拟投期刊的稿约,并大致对期刊进行浏览,了解该期刊的出版时间、出版周期、栏目设置及是否需要中英文摘要等,尽量使论文在形式上符合要求,不可漏项。

3、审稿过程中作者的配合

编辑部在接到作者的投稿后,都会寄给作者回执或发电子邮件,上面有稿件编号,作者应记住此编号,以便查询稿件处理情况。对于编辑部提出修改的稿件,一定要在规定期限内寄回,以免延误发表。论文排版后,编辑部会将校对稿寄给作者,请作者自己校对,此时一定要认真对待校对稿,有些作者错误地认为校对稿中不会有错误,因此只字不改。

4、稿件不刊用的原因分析

选题陈旧、无创新性是稿件不刊用的最主要的原因,另外所用统计方法不当也是造成退稿的原因,医学论文中统计方法使用不当是相当常见的错误,在这方面建议作者多看一些统计学书籍,正确运用统计方法,使论文合理可信。同一单位稿件集中也是造成某些稿件不能刊用的直接原因,建议同一单位相似课题的论文分散投稿,避免因稿件集中造成退稿。除以上原因外,还有因论文书写不规范,如格式不对、字迹潦草、图表、参考文献不规范等原因造成退稿。

说实话,自己投稿发表论文成功的概率是很低的,找代理成功率很高很多!医学杂志投稿

《中国医学创新》杂志是国家级正规医学学术期刊,在万方、维普及中华人民共和国新闻出版总署的网站上均可查询期刊CN号 11-5784/R 主管单位 卫生部 地址:北京市丰台区菜户营58号 财富西环15A05室《中国医学创新》杂志社邮 编: 100054投稿邮箱:

首先找医学类比较好一点的期刊吧,听听大家的建议,然后联系期刊编辑,了解相关的事宜,将你的稿件投过去审稿,审稿通过就好办了,之后就是期刊编辑们的工作了,到最后出版交版面费就可以了,试下《临床医学进展》是核心oa期刊

医学杂志帮忙查找

中国生物医学文献服务系统平台可以查到权威的医学SCI期刊信息。

2020年2月,教育部、科技部印发了《关于规范高等学校SCI论文相关指标使用 树立正确评价导向的若干意见》,该文件要破除论文“SCI至上”,也要以此为突破口,拿出针对性强、操作性强的实招硬招,破除“唯论文”,树立正确的评价导向。

50 多年来,SCI 数据库不断发展,已经成为当代世界最为重要的大型数据库,被列在国际六大著名检索系统之首。另外,随着 ISI 还陆续出版了《社会科学引文索引》(SSCI)和《艺术与人文引文索引》(A&HCI)。

它不仅是一部重要的检索工具书,而且也是科学研究成果评价的一项重要依据。它已成为目前国际上最具权威性的、用于基础研究和应用基础研究成果的重要评价体系。它是评价一个国家、一个科学研究机构、一所高等学校、一本期刊,乃至一个研究人员学术水平的重要指标之一。

SCI所收录期刊的内容主要涉及数、理、化、农、林、医、生物等基础科学研究领域,选用刊物来源于40多个国家,50多种文字,其中主要的国家有美国、英国、荷兰、德国、俄罗斯、法国、日本、加拿大等,也收录部分中国(包括港澳台)刊物。

以上内容参考:百度百科--SCI

医学杂志期刊有:1、《中国社区医师》:国内发行量最大的国家级综合性医学期刊、中国知网收录期刊、旬刊。2、《医学信息》:国内发行速度最快的国家级综合性医学期刊、中国知网收录期刊、旬刊。3、《吉林医学》:创刊历史久远,综合性医学学术期刊、旬刊、中国知网收录期刊。4、《中国医药指南》:国家级科技期刊、半月刊、中国知网收录期刊。5、《中国中医药现代远程教育》:国家级科技期刊、半月刊、中国知网收录期刊。6、《内蒙古中医药》:综合性学术期刊、旬刊、万方收据库收录期刊,职称晋升认定期刊。7、《按摩与康复医学》:国家级优秀科技期刊、中华中医药学会系列、万方数据库收录、职称晋升认定期刊。8、《中国卫生产业》:国家级医药卫生期刊、月刊、中国核心期刊(遴选)数据库收录期刊。9、《中国当代医药》:国家级医药卫生专业刊物、旬刊、中国知网收录期刊。10、《中国美容医学》:中国科技核心期刊、月刊、中国知网收录期刊。11、《中国药业》:中国科技核心期刊、半月刊、中国知网收录期刊。12、《临床合理用药杂志》:综合性医药卫生类学术期刊、半月刊、中国知网收录期刊。

帮忙翻译医学论文

你好,翻译为:“[Abstract] Objective: To compare ziprasidone and haloperidol in the treatment of schizophrenia in acute phase of the efficacy and side effects. Methods: Injection ziprasidone and haloperidol injection, the patients were randomly divided into 75 cases of ziprasidone group (n = 38) and with the haloperidol group (n = 37), for a period of five days of treatment . Respectively before and after treatment using Positive and Negative Syndrome Scale (PANSS), Clinical overall scale of India (CGI) and adverse reactions Scale (TESS) assessed the efficacy and adverse drug reactions. Pre-treatment determination of baseline ECG with QTc interval after treatment compared to baseline for more than 60ms for QTc interval prolongation ①, the treatment of cardiac rhythm during the medical examination found abnormal electrocardiogram monitoring in time. Results: Ziprasidone and haloperidol groups before and after treatment the total score and PANSS positive symptoms scale factor at a considerable reduction rate; CGI score to achieve a turn for the better and were more than 25 cases (), 26 cases of (); TESS evaluation of side effects occurred in 10 cases () 12 cases (). By T test no significant difference (P> ). Major group of ziprasidone alcohol side effects of insomnia, the main side effects of haloperidol group extrapyramidal reaction, but the ziprasidone group, 3 cases () of QTc interval prolongation, 2 cases () of cardiac rhythm disorders; haloperidol impact on the ECG for ventricular arrhythmia, was found significantly prolonged QTc interval. Conclusion: Ziprasidone injection with injection of haloperidol treatment of schizophrenia in acute phase of the effect of a considerable, but the group ziprasidone QTc interval on the heart and whether the impact of abnormal heart rate caused by a high degree of attention required.[Key words] haloperidol Ziprasidone in acute phase of schizophrenia”。

血糖升高对出血性脑卒中(hemorrhagic apoplexy)的发生发展有极其重要的影响,不但作为重要危险因素参与HA的起始,导致疾病发病率增高,而且对HA发生后病理过程有促进作用,使血肿体积扩大,加重水肿,加重功能损害,影响预后。Hyperglycemia has a very important impact on the occurrence and development of hemorrhagic stroke (hemorrhagic apoplexy). It not only acts as an important risk factor in the initiation of HA, but also increases the incidence of disease, and promotes the pathological process of HA, enlarges the volume of hematoma, aggravates edema, aggravates functional damage, and affects prognosis.高血糖参与HA的发生机制是多方面的,包括:脂代谢异常、颈动脉重塑、内皮功能障碍、血小板功能异常、高凝状态、胰岛素抵抗。而高血糖扩大梗死面积,促进HA发展主要与致酸中毒、缺血损伤区域细胞凋亡等机制有关。Hyperglycemia is involved in the pathogenesis of HA in many aspects, including: abnormal lipid metabolism, Carotid Remodeling, endothelial dysfunction, platelet dysfunction, hypercoagulability, insulin resistance. However, hyperglycemia can enlarge the infarct area and promote the development of HA, which is mainly related to the mechanism of acidosis and apoptosis in ischemic injury area.血管内皮生长因子(VEGF)和环氧合酶(COX-2)与脑血管病的关系,已引起人们的重视。血管内皮生长因子的突出作用是诱导体内血管形成,提高血管通透性;近年来发现它也有刺激神经元、胶质细胞、轴突的生长和成活的作用。环氧合酶(cyclooxygenase,COX),是催化花生四烯酸(arachidonic acid,AA)合成前列腺素(prostgalandin,PG)以及血栓素(thromboxan,TX)的限速酶。其中COX-1为结构型,存在于大多数组织中,催化生成维持正常结构的PG;COX-2为诱导型,在生理状态下,COX-2在大多数组织中以极低拷贝数表达。但IL-1、TNF等许多炎症刺激因子均可诱导COX-2表达。但目前有关血管内皮生长因子和环氧合酶的研究多集中在与脑缺血的关系上,而关于脑出血后脑水肿的动态变化与VEGF、COX-2表达的相关性研究却不多。The relationship between vascular endothelial growth factor (VEGF) and cyclooxygenase (COX-2) and cerebrovascular diseases has attracted people's attention. In recent years, it has been found that vascular endothelial growth factor can stimulate the growth and survival of neurons, glial cells and axons. Cyclooxygenase (COX) is a rate limiting enzyme that catalyzes the synthesis of prostaglandin (PG) and thromboxane (TX) from arachidonic acid (AA). COX-1 is a structural type, which exists in most tissues and catalyzes the generation of PG maintaining normal structure; COX-2 is an inducible type, which is expressed in a very low copy number in most tissues under physiological conditions. But many inflammatory factors such as IL-1 and TNF can induce COX-2 expression. However, at present, the researches on VEGF and COX-2 are mostly focused on the relationship with cerebral ischemia, but few on the relationship between the dynamic changes of brain edema and the expression of VEGF and COX-2 after cerebral hemorrhage.在认识到高血糖对脑出血损伤危害性同时,控制血糖水平治疗即成为脑血管病治疗手段之一,特别是采用胰岛素降低血糖水平纳入急性脑卒中治疗指南。已有研究发现胰岛素对急性期脑出血周围脑组织的缺血性损伤有保护作用。可能机制为:现已发现脑中存在胰岛素受体,胰岛素可与胰岛素受体结合,降低脑细胞对糖的摄取,从而降低脑细胞内糖的储存,减少乳酸产生的底物,从根本上纠正细胞酸中毒;同时胰岛素还可以降低外周血糖浓度,增加出血周围水肿带的有效血供,造成相对低血糖高灌流状态,从而对脑损害产生改善作用。In recognition of the harm of hyperglycemia to cerebral hemorrhage, the control of blood glucose level has become one of the treatment methods of cerebrovascular disease, especially the use of insulin to reduce blood glucose level has been included in the treatment guidelines of acute stroke. It has been found that insulin has a protective effect on the ischemic injury of brain tissue around acute cerebral hemorrhage. The possible mechanisms are as follows: it has been found that there is insulin receptor in the brain, insulin can combine with insulin receptor, reduce the uptake of sugar by brain cells, thus reduce the storage of sugar in brain cells, reduce the substrate produced by lactic acid, fundamentally correct cell acidosis; at the same time, insulin can also reduce the concentration of peripheral blood sugar, increase the effective blood supply of edema zone around hemorrhage, resulting in relatively low blood supply Hyperperfusion of blood glucose can improve brain damage.为了解这两种细胞因子与糖尿病合并脑出血损伤的关系,本研究在糖尿病模型的基础上,拟通过自体血注入法建立稳定的大鼠脑出血的动物模型,在此基础上动态观察脑出血后行为学和脑含水量的变化趋势,分析VEGF和COX-2在出血后脑组织中的分布特点和表达变化,进而探讨VEGF和COX-2在脑出血后脑组织损伤中的作用和意义,对比糖尿病大鼠和正常血糖大鼠脑水肿体积的差别,初步观察此二因子在糖尿病大鼠和正常血糖大鼠脑出血表达的差异,以期为脑出血的治疗提供新的方法和思路。In order to understand the relationship between these two cytokines and the injury of cerebral hemorrhage in diabetes mellitus, this study is to establish a stable animal model of cerebral hemorrhage by autogenous blood injection on the basis of diabetes model. On this basis, dynamic observation of the change trend of behavior and brain water content after cerebral hemorrhage is made, and the distribution characteristics and expression changes of VEGF and COX-2 in brain tissue after hemorrhage are analyzed, Furthermore, to explore the role and significance of VEGF and COX-2 in brain tissue injury after cerebral hemorrhage, to compare the difference of brain edema volume between diabetic rats and normal glucose rats, and to preliminarily observe the difference of expression of VEGF and COX-2 in cerebral hemorrhage between diabetic rats and normal glucose rats, in order to provide new methods and ideas for the treatment of cerebral hemorrhage.材料与方法Materials and methods1. 实验动物和分组1. Experimental animals and groups健康成年雄性Wistar大鼠,共96只,体重250~280克,由郑州大学实验动物中心提供。按照随机化的原则将实验动物分为4组,即假手术组、正常血糖组、高血糖组和胰岛素干预组。每组均设4个时间点:6h、24h、72h、7d。每个时间点设6只大鼠。96 healthy adult male Wistar rats weighing 250-280 g were provided by the experimental animal center of Zhengzhou University. According to the principle of randomization, the experimental animals were divided into four groups: sham operation group, normal blood glucose group, hyperglycemia group and insulin intervention group. Each group had four time points: 6h, 24h, 72h, 7d. Six rats were set at each time . 高血糖大鼠模型制作及胰岛素干预方法2. Establishment of hyperglycemia rat model and insulin intervention参照STZ诱导法制备高血糖大鼠模型。以STZ 60mg/kg,对高血糖及胰岛素干预组大鼠单次腹腔注射。大鼠正常血糖值为4一6mmol/L,注射后一周检测血糖≥为成功模型备选用。高血糖模型成功后,予干预组大鼠普通胰岛素,腹壁皮下注射,3次/d,4U/次,连用3天,测血糖值达正常范围。The hyperglycemia rat model was established by STZ induction. STZ (60 mg / kg) was used for single intraperitoneal injection in the hyperglycemia and insulin intervention group. The normal blood glucose value of rats was 4-6mmol / L, and the blood glucose ≥ was detected one week after injection as the successful model. After the success of hyperglycemia model, rats in the intervention group were given insulin, subcutaneous injection of abdominal wall, 3 times a day, 4U a time, for 3 days, and the blood glucose value reached the normal range.(论文翻译由学术堂提供)

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Increased Blood Sugar on hemorrhagic stroke (hemorrhagic apoplexy) the occurrence and development are very important influence, not only as an important risk factor involved in the beginning of HA, resulting in increased incidence of disease, but also to HA after the occurrence of pathological process has a catalytic role to enable hematoma volume expansion, increased edema, increased impairment, affect the blood sugar involved in the mechanism of HA, are manifold, including: lipid metabolic abnormalities, carotid artery remodeling, endothelial dysfunction, platelet dysfunction, hypercoagulability, insulin resistance. Expansion of infarct size and high blood sugar and promoting the development of HA mainly caused by acid poisoning, ischemic injury in areas of apoptosis and other endothelial growth factor (VEGF) and cyclooxygenase (COX-2) and cerebral vascular disease, has attracted people's attention. Vascular endothelial growth factor induced by the prominent role of angiogenesis in vivo and improve vascular permeability; discovered in recent years it also has to stimulate the neurons, glial cells, axonal growth and survival role. COX (cyclooxygenase, COX), is catalyzed arachidonic acid (arachidonic acid, AA) synthesis of prostaglandins (prostgalandin, PG) and thromboxane (thromboxan, TX) of the rate-limiting enzyme. One COX-1 for structural type, exist in most organizations, the catalyst is generated to maintain the normal structure of the PG; COX-2 is induced in physiological conditions, COX-2 in most tissues at very low copy number expression. However, IL-1, TNF and many other inflammation-stimulating factor can induce COX-2 expression. However, current vascular endothelial growth factor and cyclooxygenase Most studies focused on the relationship between cerebral ischemia and brain edema after intracerebral hemorrhage on the dynamic changes of VEGF, COX-2 expression in correlation among recognition of hyperglycemia on cerebral hemorrhage injury in danger at the same time, control, treatment of blood glucose levels become a means of treating cerebrovascular disease, in particular, is used to reduce blood sugar levels of insulin into the acute stroke treatment guidelines. Has been found that insulin on acute cerebral hemorrhage around the brain tissue has a protective effect of ischemic injury. Possible mechanisms are: the brain has been found that the existence of insulin receptors, insulin and insulin receptor binding may reduce the brain cells of glucose uptake, thereby reducing the storage of sugar within the brain cells, reduce lactic acid produced by the substrate, fundamentally correct cellular acidosis; the same time, can also lower blood sugar, insulin concentration, increased bleeding surrounding edema and effective blood supply, resulting in relatively low perfusion state of high blood sugar, thereby improving effect of brain damage was the order to understand these two cytokines and diabetes mellitus the relationship between cerebral hemorrhage injury, this study of diabetes on the basis of the model to be adopted by autologous blood injection method to establish a stable animal model of cerebral hemorrhage in this dynamic observation of cerebral hemorrhage on the basis of After the behavioral and brain water content trends, analysis VEGF and COX-2 in the hemorrhagic brain tissue distribution and expression changes, and then explore the VEGF and COX-2 in brain tissue damage in cerebral hemorrhage the role and significance, compared to diabetes rats and normal blood sugar difference between the volume of brain edema in rats with an initial observation of the two factors in diabetic rats and normal blood sugar difference between the expression of rat brain hemorrhage, with a view to the treatment of cerebral hemorrhage provide new ways and and methods1. Experimental animals and groupingHealthy adult male Wistar rats, a total of 96, weighing 250 to 280 grams from the Experimental Animal Center of Zhengzhou University. In accordance with the principles of randomized experimental animals were divided into four groups, namely sham operation group, normal blood glucose group, high glucose group and the insulin intervention group. Prizes will be awarded 4 points each time: 6h, 24h, 72h, 7d. At each time points are located at 6 . High blood sugar and insulin production in rat model of intervention methodsPrepared by the light of STZ-induced hyperglycemia in rats. With STZ 60mg/kg, high blood sugar and insulin in the intervention group rats a single intraperitoneal injection. Value for four rats with normal blood sugar a 6mmol / L, a week after injection, blood glucose ≥ / L for a successful model for alternative use. Model of high blood sugar after the success of the intervention group I rats were normal insulin, abdominal subcutaneous injection, 3 times / d, 4U / times qd for 3 days, the measured blood sugar value of the normal range.

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