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.

這本國際性、多學科的雜志涵蓋了兒童和成人神經(jīng)肌肉疾病的所有方面(包括肌營養(yǎng)不良、脊髓肌肉萎縮、遺傳性神經(jīng)病、先天性肌病、肌無力、強直性肌病、代謝性肌病和炎性肌病)。編輯歡迎來自各個領域的原創(chuàng)文章:臨床方面，如新的臨床實體，感興趣的案例研究，治療，管理和康復(包括生物力學，矯形設計和外科)。與臨床癥狀相關的基礎科學研究，包括分子生物學和遺傳學領域的進展。與人類疾病相關的動物模型研究。該雜志的目標是廣泛的臨床醫(yī)生，病理學家，相關的輔助醫(yī)學專業(yè)人員和臨床和基礎科學家對神經(jīng)肌肉疾病的研究感興趣。除了發(fā)表原創(chuàng)研究論文外，《華爾街日報》還發(fā)表評論和小型評論、初步的簡短通訊和書評，并設有編輯、通信和新聞版塊。還歡迎關于大會和講習班的報告，以摘要或非常全面的評論的形式提出，指出與捐助國有關的一些特別重點，并詳細說明所涉領域、重要捐助和參加者名單。該雜志為雙月刊，旨在快速出版具有科學價值和廣泛讀者興趣的高質量論文。還有一條快速出版具有突出科學價值和重要性的新材料的快車道。《神經(jīng)肌肉疾病》是世界肌肉協(xié)會的官方期刊，是一個國際性、多學科、科學的協(xié)會，致力于神經(jīng)肌肉疾病領域知識的進步和傳播。該雜志的目錄現(xiàn)在可以通過電子郵件預先發(fā)布，作為愛思唯爾科學免費內容直接服務的一部分。請發(fā)送電子郵件到cdhelp@elsevier.co。有關這項服務的更多信息，請訪問英國。