NEUROMUSCULAR DISORDERS

This international, multidisciplinary journal covers all aspects of neuromuscular disorders in childhood and adult life (including the muscular dystrophies, spinal muscular atrophies, hereditary neuropathies, congenital myopathies, myasthenias, myotonic syndromes, metabolic myopathies and inflammatory myopathies). The Editors welcome original articles from all areas of the field: Clinical aspects, such as new clinical entities, case studies of interest, treatment, management and rehabilitation (including biomechanics, orthotic design and surgery). Basic scientific studies of relevance to the clinical syndromes, including advances in the fields of molecular biology and genetics. Studies of animal models relevant to the human diseases. The journal is aimed at a wide range of clinicians, pathologists, associated paramedical professionals and clinical and basic scientists with an interest in the study of neuromuscular disorders. In addition to original research papers, the journal also publishes reviews and mini-reviews, preliminary short communications and book reviews, and has editorial, correspondence and news sections. Reports on congresses and workshops, taking the form of a digested or very comprehensive commentary, pointing out some of the particular highlights in relation to the contributors and giving some detail of the area covered, important contributions and a list of participants, are also welcome.The journal is published bi-monthly and aims at rapid publication of high quality papers of scientific merit as well as general interest to a wide readership. There is also a fast track for rapid publication of new material of outstanding scientific merit and importance. Neuromuscular Disorders is the official journal of the World Muscle Society an international, multidisciplinary, scientific society, dedicated to the advancement and dissemination of knowledge in the field of neuromuscular disorders.The table of contents for this journal is now available pre-publication, via e-mail, as part of the free ContentsDirect service from Elsevier Science. Please send an e-mail message to cdhelp@elsevier.co.uk for further information about this service.

这本国际性、多学科的杂志涵盖了儿童和成人神经肌肉疾病的所有方面(包括肌营养不良、脊髓肌肉萎缩、遗传性神经病、先天性肌病、肌无力、强直性肌病、代谢性肌病和炎性肌病)。编辑欢迎来自各个领域的原创文章:临床方面，如新的临床实体，感兴趣的案例研究，治疗，管理和康复(包括生物力学，矫形设计和外科)。与临床症状相关的基础科学研究，包括分子生物学和遗传学领域的进展。与人类疾病相关的动物模型研究。该杂志的目标是广泛的临床医生，病理学家，相关的辅助医学专业人员和临床和基础科学家对神经肌肉疾病的研究感兴趣。除了发表原创研究论文外，《华尔街日报》还发表评论和小型评论、初步的简短通讯和书评，并设有编辑、通信和新闻版块。还欢迎关于大会和讲习班的报告，以摘要或非常全面的评论的形式提出，指出与捐助国有关的一些特别重点，并详细说明所涉领域、重要捐助和参加者名单。该杂志为双月刊，旨在快速出版具有科学价值和广泛读者兴趣的高质量论文。还有一条快速出版具有突出科学价值和重要性的新材料的快车道。《神经肌肉疾病》是世界肌肉协会的官方期刊，是一个国际性、多学科、科学的协会，致力于神经肌肉疾病领域知识的进步和传播。该杂志的目录现在可以通过电子邮件预先发布，作为爱思唯尔科学免费内容直接服务的一部分。请发送电子邮件到cdhelp@elsevier.co。有关这项服务的更多信息，请访问英国。