Ataxia Investigators Meeting 2016: From Basic Science to Clinical Therapeutics
Ataxia Investigators Meeting 2016: From Basic Science to Clinical Therapeutics
批准号:
9243767
负责人:
DAVID ROBINSON LYNCH
金额:
$0.96万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-09-30 至 2016-09-29
关键词:
AddressAffectAtaxiaBasic ScienceBiologicalCerebellar degenerationClinicalClinical TrialsCollaborationsCommunicationCountryDeglutitionDiseaseEconomicsElementsEnsureEtiologyEuropeEye MovementsFamilyFloridaFoundationsFundingFutureGaitGeneticGenomicsGoalsHealthHumanIndustryInternationalLocationMovementMulti-Institutional Clinical TrialNaturePatientsPhasePostdoctoral FellowPrevalenceRecruitment ActivityResearchResearch PersonnelRouteScientific Advances and AccomplishmentsScientistSpeechTherapeuticTherapeutic Human ExperimentationTimeTranslational ResearchUnited StatesUnited States National Institutes of Healthabstractingbasedexteritygenetic approachgraduate studentlecturesmeetingsmotor controlnervous system disordernovel therapeutic interventionpostersprogramssuccesssymposiumtargeted treatmenttranslational approach
中文摘要
描述(由申请人提供):共济失调是一种致残和经常致命的神经系统疾病,由多种遗传和后天病因引起。第六届共济失调研究者会议,“AIM 2016:从基础科学到临床治疗”将汇集一个国际研究者名册,以解决共济失调的各种原因,更好地定义共济失调的致病基础,并探索治疗途径。会议将重点关注最新的科学进展和新兴的综合治疗方法,目标如下:1)确定常见的疾病机制,2)探索治疗策略,3)帮助建立共济失调研究的未来领导者,以及4)使学员(研究生和博士后)与共济失调患者和家庭接触。AIM 2016将是促进共济失调研究和治疗方法合作和讨论的关键机制,这一点尤其重要,因为该领域正在美国和欧洲进入有意义的多中心临床试验阶段。AIM 2016会议与该国最大的共济失调基金会年会在同一家酒店举行,并与之重叠,将最大限度地发挥这次会议对科学家和患者的影响。
英文摘要
DESCRIPTION (provided by applicant): Ataxia, a disabling and frequently fatal neurological disorder, results from a wide variety of genetic and acquired etiologies. The 6th Ataxia Investigators' Meeting, "AIM 2016: From Basic Science to Clinical Therapeutics" will assemble an international roster of investigators to address the diverse causes of ataxia, to define better the pathogenic basis of ataxia, and to explore routes to therapy. The conference will focus on the most recent scientific advances and emerging integrative approaches toward therapy, with the following objectives: 1) Identify common disease mechanisms, 2) Explore therapeutic strategies, 3) Help establish the future leaders of ataxia research, and 4) Bring trainees (graduate students and postdocs) into contact with ataxia patients and families. AIM 2016 will represent a critical mechanism to facilitate collaboration and discussion on ataxia research and therapeutic approaches, which is of particularly great importance now that the field is entering the phase of meaningful, multi-center clinical trials both in the United States and Europe. The AIM 2016 meeting, affiliated and overlapping with the annual meeting of the largest ataxia foundation in the country occurring at the same hotel, will maximize the impact of this meeting for scientists and patients alike.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Natural History of Friedreich ataxia in children
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批准号:10001342
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项目类别:
-
资助金额:$39.73万
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财政年份:2017
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Natural History of Friedreich ataxia in children
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批准号:10237179
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项目类别:
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资助金额:$39.95万
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财政年份:2017
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Natural History of Friedreich ataxia in children
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批准号:9770557
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项目类别:
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资助金额:$39.91万
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财政年份:2017
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Anti-NMDA receptor antibodies from patients with limbic encephalitis
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批准号:9338305
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项目类别:
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资助金额:$20.81万
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财政年份:2016
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Ataxia Investigators Meeting 2016: From Basic Science to Clinical Therapeutics
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批准号:9051026
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项目类别:
-
资助金额:$3.5万
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财政年份:2015
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Defining the epitope in anti-AMPA receptor encephalitis
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批准号:8427916
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项目类别:
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资助金额:$25.13万
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财政年份:2012
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Defining the epitope in anti-AMPA receptor encephalitis
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批准号:8544517
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项目类别:
-
资助金额:$20.2万
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财政年份:2012
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Nicotinic-glutamatergic Interactions in Axonal Development
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批准号:8269860
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项目类别:
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资助金额:$20.94万
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财政年份:2011
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Nicotinic-glutamatergic Interactions in Axonal Development
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批准号:8189649
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项目类别:
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资助金额:$23.44万
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财政年份:2011
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Defining the epitope in antiNMDA receptor encephalitis
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批准号:7919255
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项目类别:
-
资助金额:$20.36万
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财政年份:2009
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Regulation of NMDA Receptors in Excitotoxicity by Calpain and FYN
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批准号:8098037
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项目类别:
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资助金额:$36.57万
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财政年份:2003
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Calpain Mediated Cleavage of NR2 in Excitotoxicity
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批准号:6601357
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项目类别:
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资助金额:$35.18万
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财政年份:2003
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Regulation of NMDA Receptors in Excitotoxicity by Calpain and FYN
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批准号:7522453
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项目类别:
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资助金额:$38.99万
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财政年份:2003
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Regulation of NMDA Receptors in Excitotoxicity by Calpain and FYN
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批准号:7637930
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项目类别:
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资助金额:$37.35万
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财政年份:2003
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Regulation of NMDA Receptors in Excitotoxicity by Calpain and FYN
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批准号:7860694
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项目类别:
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资助金额:$36.96万
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财政年份:2003
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Calpain Mediated Cleavage of NR2 in Excitotoxicity
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批准号:6844929
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项目类别:
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资助金额:$33.91万
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财政年份:2003
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Calpain Mediated Cleavage of NR2 in Excitotoxicity
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批准号:6699302
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项目类别:
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资助金额:$34.01万
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财政年份:2003
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Regulation of NMDA Receptors in Excitotoxicity by Calpain and FYN
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批准号:7441320
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项目类别:
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资助金额:$41.25万
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财政年份:2003
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负责人:DAVID ROBINSON LYNCH
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依托单位:
Calpain Mediated Cleavage of NR2 in Excitotoxicity
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批准号:7008501
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项目类别:
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资助金额:$33.01万
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财政年份:2003
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负责人:DAVID ROBINSON LYNCH
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依托单位:
NMDA RECEPTORS, PROTEIN KINASE C, AND EXCITOTOXICITY
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批准号:2899588
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项目类别:
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资助金额:$12.05万
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财政年份:1999
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负责人:DAVID ROBINSON LYNCH
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依托单位:
海外基金