Strong Michael J, Grace Gloria M, Freedman Morris, Lomen-Hoerth Cathy, Woolley Susan, Goldstein Laura H, Murphy Jennifer, Shoesmith Christen, Rosenfeld Jeffery, Leigh P Nigel, Bruijn Lucie, Ince Paul, Figlewicz Denise
Department of Clinical Neurological Sciences, The University of Western Ontario, London, Ontario, Canada.
Amyotroph Lateral Scler. 2009 Jun;10(3):131-46. doi: 10.1080/17482960802654364.
Amyotrophic lateral sclerosis (ALS) is increasingly recognized to be a multisystem disorder which includes both clinical and neuropathological features of a frontotemporal lobar degeneration (FTLD). In order to provide a common framework within which to discuss the characteristics of the cognitive and behavioural syndromes of ALS, and with which to conduct clinical and neuropathological research, an international research workshop on frontotemporal dementia (FTD) and ALS was held in London, Canada in June 2007. The recommendations arising from this research workshop address the requirement for a concise clinical diagnosis of the underlying motor neuron disease (Axis I), defining the cognitive and behavioural dysfunction (Axis II), describing additional non-motor manifestations (Axis III) and identifying the presence of disease modifiers (Axis IV).
肌萎缩侧索硬化症(ALS)越来越被认为是一种多系统疾病,它包含额颞叶变性(FTLD)的临床和神经病理学特征。为了提供一个共同框架来讨论ALS认知和行为综合征的特征,并用于开展临床和神经病理学研究,2007年6月在加拿大伦敦举办了一场关于额颞叶痴呆(FTD)和ALS的国际研究研讨会。该研究研讨会提出的建议涉及对潜在运动神经元疾病进行简明临床诊断(轴I)、定义认知和行为功能障碍(轴II)、描述其他非运动表现(轴III)以及确定疾病修饰因子的存在(轴IV)的要求。