Society for Inherited Metabolic Disorders Annual Meeting

遗传性代谢紊乱学会年会

• 批准号: 7893627
• 负责人: NICOLA LONGO
• 金额: $ 1.1万
• 依托单位: UNIVERSITY OF UTAH
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-07-14 至 2011-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7893627
• 关键词: Affect; American; Area; Arthritis; Award; Biochemistry; Blindness; Cerebral Palsy; Clinical; Clinical Trials; Congresses; Country; Development; Diabetes Mellitus; Disease; Failure; Functional disorder; Funding; Goals; Growth; Heart Diseases; Hepatic; Inborn Errors of Metabolism; Individual; Inherited; International; Kidney; Mass Spectrum Analysis; Medical Genetics; Mental Retardation; Metabolic Diseases; Minority; Molecular; Neonatal Screening; Neuromuscular Diseases; Patient Care; Physicians; Recruitment Activity; Research; Research Personnel; Scholarship; Societies; Source; Specialist; Time; Training; Travel; United States National Institutes of Health; Woman; abstracting; college; effective therapy; meetings; programs

DESCRIPTION (Provided by Applicant): The Society for Inherited Metabolic Disorders (SIMD) requests support to provide scholarships for trainees to attend its annual meetings in years 2009 and 2010. The 2009 meeting will be held in conjunction with the International Congress on Inborn Errors of Metabolism in San Diego, CA, while the 2010 meeting will be held in Albuquerque, NM, in coordination with the annual meeting of the American College of Medical Genetics. Inborn errors of metabolism (IEM) are an important cause of mental retardation, cerebral palsy, neuromuscular disease, cardiac disorders, hepatic and renal dysfunction, arthritis, diabetes, growth failure, and blindness. As the wide clinical and molecular spectrum of these disorders is being elucidated, in part fueled by the development of tandem mass spectroscopy and the rapid expansion of newborn screening programs, the number of affected individuals is now known to be much larger than originally recognized. In addition, therapies are available for some conditions, yet few clinical trials have been performed to evaluate their efficacy. Thus, much remains to be done to better understand these severe disorders and develop effective treatments for them. For the U.S. to remain preeminent in this important area of research, it is essential to attract young investigators into the field. One effective mechanism to achieve this goal is to provide them with the opportunity to participate in the SIMD meeting, where they can explore the field and develop scientific ties to other established investigators. The SIMD meeting is held annually and participation, especially by young investigators, has been steadily increasing each year. The availability of NIH travel awards has been a major reason for this increase. Trainees seeking funding are required to submit an abstract describing original research to be presented at the meeting. The organizers anticipate submission of 40 to 50 abstracts for presentation at the annual meetings in the U.S. (2010) with two to three times that number for the international meeting (2009). Applications for travel awards will be competitively reviewed four months prior to the meeting, with the goal of making 25 annual awards of $1,000 each. Additional funds will be solicited from private sources. Women and minority applicants will be actively recruited. PROJECT NARRATIVE: The Society for Inherited Metabolic Disorders (SIMD) meeting will help to train new physicians to take care of patients with disorders of the body's biochemistry. There are very few such specialists in the country, and providing travel funds for new trainees to meet and present their research encourages them to remain in the field.

描述（由申请人提供）：遗传性代谢障碍协会（SIMD）请求支持为学员提供奖学金，以参加2009年和2010年的年会。 2009年的会议将与在加利福尼亚州圣地亚哥举行的先天性代谢缺陷国际大会一起举行，而2010年的会议将在新墨西哥州的阿尔伯克基举行，与美国医学遗传学学会年会协调。 先天性代谢缺陷（IEM）是智力迟钝、脑瘫、神经肌肉疾病、心脏病、肝肾功能障碍、关节炎、糖尿病、生长衰竭和失明的重要原因。 由于这些疾病的广泛临床和分子谱正在被阐明，部分原因是串联质谱的发展和新生儿筛查计划的快速扩展，现在已知受影响的个体数量比最初认识到的要大得多。 此外，治疗可用于某些条件，但很少进行临床试验来评估其疗效。 因此，仍有许多工作要做，以更好地了解这些严重的疾病，并开发有效的治疗方法。 美国要想在这一重要的研究领域保持领先地位，吸引年轻的研究人员进入这一领域至关重要。 实现这一目标的一个有效机制是为他们提供参加SIMD会议的机会，在那里他们可以探索该领域并与其他已建立的研究人员建立科学联系。 SIMD会议每年举行一次，参与者，特别是年轻的研究人员，每年都在稳步增加。 NIH旅行奖励的可用性是这一增长的主要原因。 寻求资助的受训者必须提交一份摘要，描述将在会议上提出的原始研究。 组织者预计在美国举行的年度会议（2010年）上将提交40至50份摘要，而国际会议（2009年）的数量将是这个数字的两至三倍。 将在会前四个月对旅行奖申请进行竞争性审查，目标是每年颁发25个每人1 000美元的旅行奖。 将从私人来源筹集更多资金。 将积极招聘妇女和少数民族申请人。 项目叙述：遗传性代谢紊乱协会（SIMD）会议将有助于培训新的医生来照顾身体生物化学紊乱的患者。 该国的这类专家很少，为新学员提供旅费，让他们见面并介绍他们的研究，鼓励他们留在这一领域。