Neurology Author Checklist
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Source: www.neurology.org, Author: Kathy Pieper
Neurology. ®. Author Checklist. This form should be used as a reference tool. Indicate that the author has received and submitted to Neurology a
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Neurology® Author Checklist
This form should be used as a reference tool. It does not replace the full information provided in the Information for Authors. Cover letter
Include title of manuscript Include classification (e.g. Article) of the manuscript. Notify editor of any possible redundant or duplicate publication. Include declaration that all authors and contributors agree to the conditions outlined in the Authorship and Contributorship section of the Information for Authors. Include statement of responsibility for clinical trial data and include date that clinical trial data must be deposited in clinical trial database (if applicable) Include statement that authors take full responsibility for the data, the analyses and interpretation, and the conduct of the research; full access to all of the data; and the right to publish any and all data. (If study is sponsored, add: separate and apart from the guidance of the sponsor.) Indicate that the Methods section includes a statement that an IRB or regional review board has approved the use of human subjects for this study Indicate that that the author has received permission to cite any personal communications (if applicable). Indicate that the author has received and submitted to Neurology a Patient Consent-to-Disclose Form for any figure or video of a recognizable patient.
Methods In a subsection on Standard Protocol Approvals, Registrations, and Patient Consents, include the following (if applicable):
A statement that approval was received by an ethical standards committee on human experimentation (institutional or regional) for any experiments using human subjects. A statement that written informed consent was obtained from all patients (or guardians of patients) participating in the study. Indicate that a signed Patient Consent-to-Disclose Form has been obtained for photos/ videos of any recognizable patient. If reporting a clinical trial, provide the identity of the public trials registry and the clinical trial identifier number.
Body of Manuscript
Use 12 pt. font size. Use a default typeface (e.g.,Times, Times New Roman, Courier, Helvetica or Arial). Set the left margin at one inch and the right margin at one-half inch or more. Do not justify the right margin; leave it unaligned. Place the page number and lead author's last name in the upper right corner of each page (including the reference, tables, and figure legend(s) pages).
Title Page
Provide a clinically interesting and informative title (96 characters or less, including spaces punctuation, and subtitle). Use Widely Accepted Abbreviations in title. Include word counts for Abstract and text and character count for the title. Include number of references, tables and figures. Include all authors with highest degrees and institutions. Provide full contact information for the corresponding author and email addresses of all co-authors. Specify who completed the statistical analysis and list affiliation(s). Indicate if there are “supplementary data” to the manuscript. Provide five or fewer Search Terms accompanied by their corresponding numbers.
Results
Evidence-based medicine statistics (if applicable) must be included for the manuscript to be forwarded for editorial review including confidence intervals, numbers needed to treat, and absolute risk reduction
References
The references (check classification for maximum number) should be numbered and listed in the order cited. If references include more than six authors, cite only the first three and add et al. If there are six or fewer authors, cite all of them. Use continuous pagination (e.g., 33-37, not 33-7).
Page 2
List disclosures of all authors. Indicate if study is industry-sponsored; if so, list sponsors. If one or more authors have no disclosures, include the following: “Dr. John Doe reports no disclosures.”
Figures
If submitting a randomized clinical trial (CONSORT) or a study reporting diagnostic accuracy (STARD), the flow chart should be figure 1. JPG , PPT, PDF, and GIF files may be submitted for review purposes only. Digital files must be saved at the size authors would like them to appear in print. Keys should be within the confines of the figure or included in the figure legend. The figure legend and a title of no more than 15 words should be placed on a separate page of the manuscript document. Indicate figures that are to be published online-only.
Forms and Checklists
Upon request for revisions, each author must complete an interactive Authorship Agreement Form and a Disclosure Agreement Form. For randomized, controlled clinical trials, submit a completed Consolidated Standards for Reporting Trials (CONSORT) checklist. For studies on diagnostic accuracy, submit a completed Standards for Reporting of Diagnostic (STARD) checklist. For meta-analyses of observational studies, submit a completed Meta-analysis Of Observational Studies in Epidemiology (MOOSE) checklist. For case-control, cohort, and cross-sectional observational studies, submit a completed STROBE checklist.
Abstract
Abstracts should not exceed 250 words. A structured Abstract is mandatory for Articles. (Clinical/Scientific Notes do not have Abstracts). Include Classification of Evidence for therapeutic papers.
Supplemental Data (Upload as supplemental files)
Cited ‘in press’ articles Videos and video legends CONSORT, STARD, STROBE, MOOSE checklists Tables and Figures for online-only publication Patient Consent-to-Disclose Form for recognizable patients
Drugs and Devices
State generic name with proprietary name, city, & state of manufacturer in parentheses at first mention, generic name thereafter.
Videos
Videos must be 10MB or less. Preferred video formats include .wma, .mpg and .mov files.
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