首页 > 最新文献

Future Neurology最新文献

英文 中文
A natural human monoclonal antibody protects from axonal injury in different CNS degenerative disease models 一种天然人单克隆抗体在不同中枢神经系统退行性疾病模型中保护轴突免受损伤
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2018-02-01 DOI: 10.2217/FNL-2017-0027
Ahmad Kunbaz, A. Warrington, M. Perwein, Mahboobeh Fereidan-Esfahani, Moses Rodriguez
{"title":"A natural human monoclonal antibody protects from axonal injury in different CNS degenerative disease models","authors":"Ahmad Kunbaz, A. Warrington, M. Perwein, Mahboobeh Fereidan-Esfahani, Moses Rodriguez","doi":"10.2217/FNL-2017-0027","DOIUrl":"https://doi.org/10.2217/FNL-2017-0027","url":null,"abstract":"","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"13 1","pages":"23-29"},"PeriodicalIF":1.3,"publicationDate":"2018-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/FNL-2017-0027","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41912840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
What goes up must come down: homeostatic synaptic plasticity strategies in neurological disease. 上升的必然下降:神经系统疾病中的稳态突触可塑性策略。
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2018-02-01 Epub Date: 2018-01-17 DOI: 10.2217/fnl-2017-0028
Emily A André, Patrick A Forcelli, Daniel Ts Pak

Brain activity levels are tightly regulated to minimize imbalances in activity state. Deviations from the normal range of activity are deleterious and often associated with neurological disorders. To maintain optimal levels of activity, regulatory mechanisms termed homeostatic synaptic plasticity establish desired 'set points' for neural activity, monitor the network for deviations from the set point and initiate compensatory responses to return activity to the appropriate level that permits physiological function [1,2]. We speculate that impaired homeostatic control may contribute to the etiology of various neurological disorders including epilepsy and Alzheimer's disease, two disorders that exhibit hyperexcitability as a key feature during pathogenesis. Here, we will focus on recent progress in developing homeostatic regulation of neural activity as a therapeutic tool.

大脑活动水平受到严格调节,以尽量减少活动状态的不平衡。偏离正常活动范围是有害的,通常与神经系统疾病有关。为了维持最佳的活动水平,被称为稳态突触可塑性的调节机制为神经活动建立了理想的“设定点”,监测网络是否偏离设定点,并启动代偿反应,将活动恢复到允许生理功能的适当水平[1,2]。我们推测,体内平衡控制受损可能导致多种神经系统疾病的病因,包括癫痫和阿尔茨海默病,这两种疾病在发病过程中表现出高兴奋性是一个关键特征。在这里,我们将重点介绍神经活动的稳态调节作为一种治疗工具的最新进展。
{"title":"What goes up must come down: homeostatic synaptic plasticity strategies in neurological disease.","authors":"Emily A André,&nbsp;Patrick A Forcelli,&nbsp;Daniel Ts Pak","doi":"10.2217/fnl-2017-0028","DOIUrl":"https://doi.org/10.2217/fnl-2017-0028","url":null,"abstract":"<p><p>Brain activity levels are tightly regulated to minimize imbalances in activity state. Deviations from the normal range of activity are deleterious and often associated with neurological disorders. To maintain optimal levels of activity, regulatory mechanisms termed homeostatic synaptic plasticity establish desired 'set points' for neural activity, monitor the network for deviations from the set point and initiate compensatory responses to return activity to the appropriate level that permits physiological function [1,2]. We speculate that impaired homeostatic control may contribute to the etiology of various neurological disorders including epilepsy and Alzheimer's disease, two disorders that exhibit hyperexcitability as a key feature during pathogenesis. Here, we will focus on recent progress in developing homeostatic regulation of neural activity as a therapeutic tool.</p>","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"13 1","pages":"13-21"},"PeriodicalIF":1.3,"publicationDate":"2018-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/fnl-2017-0028","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35776204","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Prehospital notification can effectively reduce in-hospital delay for thrombolysis in acute stroke 院前告知可有效减少急性脑卒中溶栓的住院延误
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2018-02-01 DOI: 10.2217/FNL-2017-0031
Elyar Sadeghi-Hokmabadi, M. Farhoudi, A. Taheraghdam, R. Rikhtegar, R. Ghafouri, Rogayyeh Asadi, Elham Mehdizadeh Far, N. Ghaemian, Mehrdad Mehrara, Reshad Mirnour
Aim: To reduce in-hospital intervals by developing a prehospital notification (PHN) protocol which directly notifies a neurologist to prepare for possible treatment. Methods: A 24/7 connection was established between emergency medical services dispatch and the on-call neurologist. A database of all patients with in-hospital stroke code activation was developed, door-to-computed tomography (CT) time and door-to-needle time was recorded from January 2013 to December 2016. The statistical results were considered significant at p < 0.05. Result: PHN resulted in a significant reduction in door-to-CT time (median 14 vs 20; p < 0.001). Among patients who were treated with intravenous thrombolysis, door-to-needle time was significantly shorter in patients with PHN compared with non-PHN group (median 42 vs 70; p < 0.001). Conclusion: PHN effectively reduced door-to-CT and door-to-needle times. © 2018 2018 Reshad Mirnour.
目的:通过制定院前通知(PHN)协议,直接通知神经科医生为可能的治疗做准备,以减少住院间隔。方法:在紧急医疗服务调度和随叫随到的神经科医生之间建立全天候的联系。建立了所有院内卒中代码激活患者的数据库,记录了2013年1月至2016年12月期间门对计算机断层扫描(CT)时间和门对针头时间。p < 0.05为差异有统计学意义。结果:PHN可显著缩短门静脉到ct的时间(中位14 vs 20;P < 0.001)。在接受静脉溶栓治疗的患者中,PHN患者从门到针的时间明显短于非PHN组(中位数42 vs 70;P < 0.001)。结论:PHN可有效减少门到ct和门到针的次数。©2018 2018 Reshad mirour。
{"title":"Prehospital notification can effectively reduce in-hospital delay for thrombolysis in acute stroke","authors":"Elyar Sadeghi-Hokmabadi, M. Farhoudi, A. Taheraghdam, R. Rikhtegar, R. Ghafouri, Rogayyeh Asadi, Elham Mehdizadeh Far, N. Ghaemian, Mehrdad Mehrara, Reshad Mirnour","doi":"10.2217/FNL-2017-0031","DOIUrl":"https://doi.org/10.2217/FNL-2017-0031","url":null,"abstract":"Aim: To reduce in-hospital intervals by developing a prehospital notification (PHN) protocol which directly notifies a neurologist to prepare for possible treatment. Methods: A 24/7 connection was established between emergency medical services dispatch and the on-call neurologist. A database of all patients with in-hospital stroke code activation was developed, door-to-computed tomography (CT) time and door-to-needle time was recorded from January 2013 to December 2016. The statistical results were considered significant at p < 0.05. Result: PHN resulted in a significant reduction in door-to-CT time (median 14 vs 20; p < 0.001). Among patients who were treated with intravenous thrombolysis, door-to-needle time was significantly shorter in patients with PHN compared with non-PHN group (median 42 vs 70; p < 0.001). Conclusion: PHN effectively reduced door-to-CT and door-to-needle times. © 2018 2018 Reshad Mirnour.","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"13 1","pages":"5-11"},"PeriodicalIF":1.3,"publicationDate":"2018-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/FNL-2017-0031","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42898121","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Comorbid autism spectrum disorder and anxiety disorders: a brief review. 自闭症谱系障碍与焦虑症并发症:简要回顾。
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2018-02-01 Epub Date: 2018-01-17 DOI: 10.2217/fnl-2017-0030
Brian A Zaboski, Eric A Storch

Appearing in 40% of the cases of autism spectrum disorder (ASD), comorbid anxiety presents unique challenges for practitioners by amplifying problem behaviors such as social skills deficits, resistance to change and repetitive behaviors. Furthermore, comorbid ASD/anxiety strains familial relationships and increases parental stress. Research indicates that the neurobiological interactions between anxiety and ASD require comprehensive assessment approaches, modified cognitive behavioral therapy and carefully managed pharmacological interventions. Meta-analyses indicate that cognitive behavioral therapy with exposure is an effective treatment option when adequately accounting for social, familial and cognitive variables. The purpose of this focused review is to update readers on the latest research advances in comorbid ASD and anxiety, including prevalence, assessment, psychosocial and pharmacological treatment.

40% 的自闭症谱系障碍(ASD)患者会合并焦虑症,焦虑症会放大患者的问题行为,如社交技能缺陷、抗拒改变和重复行为等,从而给从业人员带来独特的挑战。此外,并发 ASD/焦虑症还会使家庭关系紧张,增加父母的压力。研究表明,焦虑和 ASD 之间的神经生物学相互作用需要全面的评估方法、改良的认知行为疗法和精心管理的药物干预。元分析表明,在充分考虑社会、家庭和认知变量的情况下,暴露认知行为疗法是一种有效的治疗方案。本重点综述旨在向读者介绍有关合并 ASD 和焦虑症的最新研究进展,包括患病率、评估、社会心理和药物治疗。
{"title":"Comorbid autism spectrum disorder and anxiety disorders: a brief review.","authors":"Brian A Zaboski, Eric A Storch","doi":"10.2217/fnl-2017-0030","DOIUrl":"10.2217/fnl-2017-0030","url":null,"abstract":"<p><p>Appearing in 40% of the cases of autism spectrum disorder (ASD), comorbid anxiety presents unique challenges for practitioners by amplifying problem behaviors such as social skills deficits, resistance to change and repetitive behaviors. Furthermore, comorbid ASD/anxiety strains familial relationships and increases parental stress. Research indicates that the neurobiological interactions between anxiety and ASD require comprehensive assessment approaches, modified cognitive behavioral therapy and carefully managed pharmacological interventions. Meta-analyses indicate that cognitive behavioral therapy with exposure is an effective treatment option when adequately accounting for social, familial and cognitive variables. The purpose of this focused review is to update readers on the latest research advances in comorbid ASD and anxiety, including prevalence, assessment, psychosocial and pharmacological treatment.</p>","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"13 1","pages":"31-37"},"PeriodicalIF":1.3,"publicationDate":"2018-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772195/pdf/fnl-13-31.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35776205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Traumatic brain injuries in victims of intimate partner violence: an underappreciated source of neurological morbidity 亲密伴侣暴力受害者的创伤性脑损伤:一个未被重视的神经系统疾病来源
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2017-12-01 DOI: 10.2217/FNL-2017-0026
K. Monahan, Andrew M. Goldfine, A. Biegon
{"title":"Traumatic brain injuries in victims of intimate partner violence: an underappreciated source of neurological morbidity","authors":"K. Monahan, Andrew M. Goldfine, A. Biegon","doi":"10.2217/FNL-2017-0026","DOIUrl":"https://doi.org/10.2217/FNL-2017-0026","url":null,"abstract":"","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"12 1","pages":"189-191"},"PeriodicalIF":1.3,"publicationDate":"2017-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/FNL-2017-0026","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46515038","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Celebrating 50 years of neuroscience research at Lilly's Erl Wood site 庆祝礼来公司厄尔伍德基地神经科学研究50周年
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2017-12-01 DOI: 10.2217/FNL-2017-0023
Adam Price-Evans
{"title":"Celebrating 50 years of neuroscience research at Lilly's Erl Wood site","authors":"Adam Price-Evans","doi":"10.2217/FNL-2017-0023","DOIUrl":"https://doi.org/10.2217/FNL-2017-0023","url":null,"abstract":"","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"12 1","pages":"193-198"},"PeriodicalIF":1.3,"publicationDate":"2017-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/FNL-2017-0023","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46298559","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pharmacotherapy of personality disorders: what we know and what we have to search for 人格障碍的药物治疗:我们所知道的和我们必须寻找的
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2017-12-01 DOI: 10.2217/FNL-2017-0010
P. Bozzatello, Camilla Ghirardini, Maria Uscinska, P. Rocca, S. Bellino
Pharmacotherapy for personality disorders is in the early stage of development because the evidence base for effective drug treatment is insufficient, biased toward borderline personality disorder and rampant with methodological issues. In this paper, we reviewed randomized, placebo-controlled trials of drugs efficacy in patients with personality disorders published between 1990 and 2016. Overwhelming majority of studies focused on borderline personality disorder (BPD), and the accumulation of evidence resulted in 7 meta-analyses, which are interpreted into better strategies for evidence-based practice. Little research attention was given to schizotypal (SPTD) and antisocial (ASPD) personality disorders, with only indirect treatment efficacy evidence for the obsessive-compulsive (OCPD) and avoidant (AvPD) personality disorders. Some avenues for future efficacy research are indicated. respectively on a fair (level B) and minimal (level C) research-based evidence level. The main symptomatic targets of pharmacotherapy in personality disorders, according to WFSBP guidelines, are affective dysregulation, cognitive-perceptual symptoms, impulsivity and anger. The effects of pharmacotherapy in these patients can also be useful to increase response to combined psychosocial interventions.
人格障碍的药物治疗处于发展的早期阶段,因为有效药物治疗的证据基础不足,偏向于边缘型人格障碍,并且方法论问题猖獗。在这篇论文中,我们回顾了1990年至2016年间发表的关于人格障碍患者药物疗效的随机安慰剂对照试验。绝大多数研究都集中在边缘型人格障碍(BPD)上,证据的积累导致了7项荟萃分析,这些分析被解释为循证实践的更好策略。很少有研究关注分裂型(SPTD)和反社会型(ASPD)人格障碍,只有强迫症(OCPD)和回避型(AvPD)人格障碍的间接治疗疗效证据。指出了未来疗效研究的一些途径。分别在基于公平(B级)和最低(C级)研究的证据水平上。根据WFSBP指南,人格障碍药物治疗的主要症状靶点是情感失调、认知感知症状、冲动和愤怒。药物治疗对这些患者的影响也有助于提高对联合心理社会干预的反应。
{"title":"Pharmacotherapy of personality disorders: what we know and what we have to search for","authors":"P. Bozzatello, Camilla Ghirardini, Maria Uscinska, P. Rocca, S. Bellino","doi":"10.2217/FNL-2017-0010","DOIUrl":"https://doi.org/10.2217/FNL-2017-0010","url":null,"abstract":"Pharmacotherapy for personality disorders is in the early stage of development because the evidence base for effective drug treatment is insufficient, biased toward borderline personality disorder and rampant with methodological issues. In this paper, we reviewed randomized, placebo-controlled trials of drugs efficacy in patients with personality disorders published between 1990 and 2016. Overwhelming majority of studies focused on borderline personality disorder (BPD), and the accumulation of evidence resulted in 7 meta-analyses, which are interpreted into better strategies for evidence-based practice. Little research attention was given to schizotypal (SPTD) and antisocial (ASPD) personality disorders, with only indirect treatment efficacy evidence for the obsessive-compulsive (OCPD) and avoidant (AvPD) personality disorders. Some avenues for future efficacy research are indicated. respectively on a fair (level B) and minimal (level C) research-based evidence level. The main symptomatic targets of pharmacotherapy in personality disorders, according to WFSBP guidelines, are affective dysregulation, cognitive-perceptual symptoms, impulsivity and anger. The effects of pharmacotherapy in these patients can also be useful to increase response to combined psychosocial interventions.","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"12 1","pages":"199-222"},"PeriodicalIF":1.3,"publicationDate":"2017-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/FNL-2017-0010","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45498492","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Genetics of Alzheimer's disease: an update 阿尔茨海默病遗传学研究进展
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2017-12-01 DOI: 10.2217/FNL-2017-0003
M. Tang, C. Reitz
{"title":"Genetics of Alzheimer's disease: an update","authors":"M. Tang, C. Reitz","doi":"10.2217/FNL-2017-0003","DOIUrl":"https://doi.org/10.2217/FNL-2017-0003","url":null,"abstract":"","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"12 1","pages":"237-247"},"PeriodicalIF":1.3,"publicationDate":"2017-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/FNL-2017-0003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45529508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Penumbral freeze: travel distance and delays provide an opportunity to study prerecanalization therapy neuroprotection 半影冻结:移动距离和延迟提供了研究预通管治疗神经保护的机会
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2017-12-01 DOI: 10.2217/FNL-2017-0025
D. Blacker
{"title":"Penumbral freeze: travel distance and delays provide an opportunity to study prerecanalization therapy neuroprotection","authors":"D. Blacker","doi":"10.2217/FNL-2017-0025","DOIUrl":"https://doi.org/10.2217/FNL-2017-0025","url":null,"abstract":"","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"12 1","pages":"185-188"},"PeriodicalIF":1.3,"publicationDate":"2017-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/FNL-2017-0025","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42669288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Fragile X–tremor/ataxia syndrome: five areas of new development 脆性震颤/共济失调综合征:五个新发展领域
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2017-12-01 DOI: 10.2217/FNL-2017-0019
Ajal Dave, J. Hawley
{"title":"Fragile X–tremor/ataxia syndrome: five areas of new development","authors":"Ajal Dave, J. Hawley","doi":"10.2217/FNL-2017-0019","DOIUrl":"https://doi.org/10.2217/FNL-2017-0019","url":null,"abstract":"","PeriodicalId":12606,"journal":{"name":"Future Neurology","volume":"12 1","pages":"249-260"},"PeriodicalIF":1.3,"publicationDate":"2017-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/FNL-2017-0019","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48933807","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Future Neurology
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1