Clinical movement disorders – a new era
نویسنده
چکیده
We are proud to announce the launch of a new open access journal, entitled Journal of Clinical Movement Disorders (JCMD). The aim of the journal is to offer an open access forum for the publication of scientifically rigorous articles focusing on the natural history, etiology, evaluation and treatment of patients with a wide range of movement disorders [1]. We are interested in topics important to the practicing clinician, but especially in articles that explore the ways in which translational approaches are changing the evaluation and treatment of patients with movement disorders in the 21 century. We are particularly pleased to launch JCMD as a fully open access journal. At present, only one journal devoted to movement disorders (Tremor and Other Hyperkinetic Disorders) offers an open access format. We believe that the open access format offers numerous advantages to traditional publication strategies. Articles will be published as soon as they are accepted, markedly decreasing the time for evaluation and distribution. All articles are available online at no cost throughout the world, enabling the widest possible reach for the journal irrespective of a reader’s location or economic resources [2]. Authors will continue to hold copyright for their work, and articles will be archived in PubMed Central. The online format allows articles to be published without constraints on length of text. Further, the format is a perfect vehicle for publication of videos demonstrating salient features in articles, a critical feature of clinical movement disorders. JCMD will publish articles covering the full spectrum of movement disorders including hypokinetic disorders (Parkinson’s disease, atypical parkinsonian disorders such as multiple system atrophy, progressive supranuclear palsy, corticobasal syndrome, dementia with Lewy body disease, frontotemporal dementia, etc.), and usual and unusual hyperkinetic disorders (myoclonus, chorea, tics, tremor, dystonia, stereotypies, paroxysmal movement disorders, etc.). We are interested in both descriptive articles that illustrate phenotype, as well as hypothesis driven articles that explore the etiology, genetics, pharmacology,
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