The 3rd World Parkinson Congress is a four-day scientific conference designed to

描述(由申请人提供)：第三届世界帕金森大会(WPC 2013)的目的是满足持续的全球对话的需要，就帕金森病(PD)的多方面问题进行对话，并提出解决方案，包括新的研究方法和更好的帕金森病患者护理模式。2013年世界帕金森病大会将于2013年10月1日至4日在加拿大蒙特利尔举行，这是帕金森病领域唯一一次将整个帕金森病社区聚集在一起举行高级别科学和非正式会议的国际会议。与会代表包括来自近60个国家的神经学家、内科医生、帕金森病患者、护理人员、护士、康复专家、政府代表和倡导团体成员。为期四天的计划突出了帕金森病科学的进步和对患有这种疾病的人的护理模式。让美国的研究人员接触到世界其他地区取得的科学进步，将有助于他们探索新想法，并建立他们原本可能不会考虑的合作。民主党社区的广泛支持和参与(已经有140多个合作组织和少数赞助商)表明，WPC是这些广泛分布的团体会面和建立合作的合适场所。它将允许和鼓励卫生专业人员、研究人员以及帕金森病患者和照顾者之间的互动，否则他们可能不会见面。这种思想的相互交融将刺激新的创新研究，为未得到满足的需求确定潜在的解决方案，推动帕金森氏症患者的治疗，并激励代表们继续他们的工作。包括帕金森病患者(PWP)在内的49名委员会成员设计了一项关于帕金森病独特方面的精心设计的计划，以深化研究人员/临床医生对帕金森病研究的承诺，并促进对帕金森病研究较少的方面的研究。该计划预计将使PwP和照顾者接触到研究，并增加参与临床试验的兴趣。扬声器 正在邀请来自PD社区所有领域的人员举办会议，以最大限度地发挥学习潜力和进行对话，包括大中型讲习班以及更亲密的讲习班。上午的全体会议将着眼于神经元死亡、非运动表现以及对帕金森病管理的新观点。这将为今后会议的进一步讨论奠定每天的基础。每天都会展示科学版和帕金森氏症生活版的海报。海报会议和巡回演出旨在最大限度地促进代表之间的互动。每天在基础和临床研究、临床治疗和生活质量方面最杰出的四张海报将以口头形式呈现在热门话题中，并将举行海报巡回演出，密切关注这一领域最有前途的工作，并加强社区的对话和合作。

DESCRIPTION (provided by applicant): The purpose of the 3rd World Parkinson Congress (WPC 2013) is to address an ongoing need for worldwide dialogue on the multifaceted problems of Parkinson's disease (PD) and to propose solutions, including new approaches to research and better models of care for people with PD. The WPC 2013, to be held from October 1-4, 2013, in Montreal, Canada, is the only international meeting in the field of Parkinson's that brings the whole PD community together for high-level scientific and lay sessions. Delegates at the meeting represent neuroscientists, physicians, people with PD, caregivers, nurses, rehabilitation specialists, government representatives, and members of the advocacy community from nearly 60 countries. The four-day program highlights advancements in the science of PD and models of care for people living with the disease. Exposing researchers from the US to the scientific advancements made in other parts of the world will help them explore new ideas and build collaborations they might otherwise not have considered. Broad support and involvement from the PD community (already over 140 partnering organizations and a handful of sponsors) shows that the WPC is the right venue for these widespread groups to meet and build collaborations. It will allow and encourage interactions between health professionals, researchers, and people with PD and caregivers who might not otherwise meet. Such inter-digitation of ideas will spur new innovative research, identify potential solutions to unmet needs, advance therapies for people with PD and inspire delegates to continue their work. Forty-nine committee members, including people with PD (PwP), designed an elaborate program about unique aspects of PD to deepen the commitment of researchers/clinicians to PD research and foster research on less studied aspects of PD. The program is expected to expose PwPs and caregivers to research and increase interest in participating in clinical trials. Speakers are being invited from all areas of the PD community with sessions formatted to maximize the learning potential and dialogue, including large and moderately sized as well as more intimate workshops. The morning plenaries will look at the death of neurons, non-motor manifestations, and new views on management of PD. This will set the stage daily for further discussion in later sessions. There will be both Scientific and Living with Parkinson's posters displayed each day. Poster sessions and tours are designed to maximize interaction among the delegates. The four most outstanding posters each day in basic and clinical research, clinical therapeutics and quality of life will be presented in an oral "Hot Topics" session and poster tours will be held, paying keen attention to the most promising work in the field and to increase dialogue and collaboration in the community.