Guide for Authors
PM&R INSTRUCTIONS FOR AUTHORSSUBMISSION CATEGORIESMANUSCRIPT REVISIONS
PM&R is the official scientific journal of the American Academy of Physical Medicine and Rehabilitation (AAPM&R). It is a monthly, peer reviewed, scholarly publication. It aims to be an internationally leading journal that advances education and impacts the specialty of physical medicine and rehabilitation through the timely delivery of clinically relevant and evidence-based research and review information. Contributions from all parts of the world and from all types of professions in rehabilitation are therefore encouraged.
Topics covered include acute and chronic musculoskeletal disorders and pain, neurologic conditions involving the central and peripheral nervous systems, rehabilitation of impairments associated with disabilities in adults and children, and neurophysiology and electrodiagnosis. PM&R emphasizes principles of injury, function, and rehabilitation, and is designed to be relevant to practitioners and researchers in a variety of medical and surgical specialties and rehabilitation disciplines including allied health. Submission of manuscripts is encouraged from physiatrists, physicians, and researchers in related disciplines, and other multidisciplinary rehabilitation professionals such as physical therapists, occupational therapists, psychologists, neuropsychologists and speech and language therapists.The content of PM&R includes articles that are contemporary and important to both research and clinical practice in physical medicine and rehabilitation. The various sections of the journal highlight original research including clinical trials and outcomes studies, studies on various methodology including rehabilitation technology, outcome measurements and epidemiology on disability related to rehabilitation, clinically relevant translational science, comprehensive and focused review articles, case presentations, point/counterpoint debates and commentary, ethical legal topics, practice management updates, editorial and opinion pieces, images, clinical pearls, emerging issues, and publication-related letters to the editor.
PM&R emphasizes principles of injury, function, and rehabilitation, and is designed to be relevant to practitioners and researchers in a variety of medical and surgical specialties and rehabilitation disciplines. Submission of manuscripts is encouraged from physiatrists, physicians, and researchers in related disciplines, and other multidisciplinary rehabilitation professionals.The content of PM&R includes articles that are contemporary and important to both research and clinical practice. The various sections of the journal highlight original research including clinical trials and outcomes studies, clinically relevant translational science, comprehensive and focused review articles, case presentations, point/counterpoint debates and commentary, ethical legal topics, practice management updates, editorial and opinion pieces, images, clinical pearls, emerging issues, and publication-related letters to the editor.http://ees.elsevier.com/pmrjournal. First-time users: Please click the Register button from the main menu and enter the requested information. For those previously registered with EES (for other Elsevier journals), please be advised that registration for PM&R is still required as the EES database is separate and distinct for each journal. This registration process is required one time only. On successful registration, you will be sent an e-mail indicating your user name and password, which can thereafter be modified to your preference.http://ees.elsevier.com/pmrjournal. It may be uploaded electronically with the manuscript, or emailed to email@example.com.
This form stipulates the following: author(s)' warranty of responsibilities, author(s)' rights, copyright transfer agreement, exclusive publication statement, disclosure of conflict of interest, adherence to Institutional Review Board (IRB) or animal care committee policies (if applicable), identification of funding source (including National Institutes of Health status, if applicable), and device status (if applicable).YOUR MANUSCRIPT WILL NOT PROCEED WITH THE REVIEW PROCESS UNTIL THE COMPLETED FORM IS RECEIVED BY THE EDITORIAL OFFICE.
Corresponding Author: A single author of the manuscript is required to serve as the primary correspondent with the PM&R editorial office, to accept responsibility for addressing revision recommendations from PM&R reviewers and editors, to review final page proofs, and to make decisions regarding release of information to media outlets or government agencies. The corresponding author is also responsible for providing statistical data if requested by the editor-in-chief and is responsible for identifying names, addresses and affiliations of all undisclosed writers who have contributed to this submitted manuscript. All authors must agree ahead of manuscript submission the identity of the corresponding author designee.Author(s)' Warranty: Any person listed as a manuscript author should have made substantive intellectual contributions to the study as established by the International Committee of Medical Journal Editors (ICMJE, www.icmje.org). All authors should meet all of the following conditions with regard to the manuscript: (1) substantial contributions to conception and design, or acquisition of data, or analysis and interpretation of data; (2) drafting the article or revising it critically for important intellectual content; (3) final approval of the version to be published; and (4) taking public responsibility for its content. PM&R may require authors to justify the assignment of authorship.
Multi-center trials present a unique situation in which a single corporate author is not acceptable. All members of the group who are named as authors, either in the authorship position below the title or in a footnote, must fully meet the criteria for authorship as defined. Group members not meeting these criteria should be listed, with their permission, in the acknowledgments. Permission must be obtained in writing from persons acknowledged for contributions other than technical, secretarial or financial support. The authors warrant that the entire manuscript is an original product of the author(s) and represents honest and valid work. Finally, the order of authorship is a joint decision of, and must have been agreed to by, all of the authors.Author(s)' Rights: The AAPM&R hereby licenses the following rights back to the author(s):
- (1) Patent and trademark rights to any process or procedure described in the article;
(2) The right to photocopy or make single electronic copies of the article for their own personal use, including for teaching purposes within an educational environment, or for the personal use of colleagues, provided that the copies are not sold or systematically distributed in paper or electronically. Posting of the article on a secure network (not accessible to the public) within the author(s)' home institution is permitted;
(3) The right, subsequent to electronic or print publication, to use the article or any part thereof, free of charge in a printed compilation of works of their own, such as collected writings or lecture notes.
Note: All copies, paper or electronic, or other use of the information include an indication of the AAPM&R copyright and a full citation of the journal source.
Copyright Transfer Agreement: In consideration of the action of PM&R reviewing, editing and accepting this manuscript (including text, tables, figures, audio, video and/or other supplemental files) for publication, the author(s) agree to transfer, assign, or otherwise convey all copyright ownership, including any and all rights incidental thereto, exclusively to the AAPM&R, in the event that this work is published in PM&R. If your manuscript is not accepted for publication, then all said rights return to the author(s). For officers or employees of the U.S. government, AAPM&R recognizes that works prepared as part of their official government duties are in the public domain, but they must still sign the Conditions for Submission form.Exclusive Publication Statement: The author(s) certify that this manuscript and the material within this manuscript have not been previously published in print or electronic formats in part or in whole, nor is this manuscript and materials within this manuscript currently under consideration for publication elsewhere. This includes symposia, transactions, books, journals, invited articles, and preliminary publications. This restriction does not apply to abstracts of less than 500 words or press reports published in conjunction with scientific meetings.
Disclosure of Conflict of Interest: Each author has reviewed PM&R's policy on Conflict of Interest and has completed the Disclosure Form (at http://ees.elsevier.com/pmrjournal ) which must be returned to the PM&R editorial office along with the Conditions for Submission Form. A notation of a conflict of interest will be included as a footnote on the first page of the article.Human Studies: It is the author's responsibility to ensure that a patient's anonymity be carefully protected and to verify that any experimental investigation with human subjects reported in the manuscript was performed with informed consent and following all the guidelines for experimental investigation with human subjects required by the institution(s) with which all the authors are affiliated. Authors should mask patients' face and remove patients' names from figures unless they obtain written consent from the patients and submit written consent with the manuscript.
Authors from US institutions must comply with all regulations of the Health Insurance Portability and Accountability Act (HIPAA) of 1996.If an IRB exists at the institution(s) in which any study involving human subjects is conducted, the investigators must obtain prior approval. This requirement applies to prospective and retrospective studies (including technical notes and case reports) that involve any direct interaction with patients OR evaluation or review of private information (eg, imaging studies or chart reviews).
If the IRB at the participating institution does not require approval for the type of research being performed, a statement to this effect must be included in the manuscript. If no IRB existed at the time the study was initiated, the authors must include a statement in the manuscript indicating as such and that principles of the Declaration of Helsinki (http://ohsr.od.nih.gov/guidelines/helsinki.html ) were followed. If a manuscript reports on the emergent use of a material or device not approved by the Food and Drug Administration or accepted as standard of practice, the authors must state that they obtained informed consent from the patient (when feasible) and reported the case to the local IRB within 1 week of the event. This procedure is only valid for a single patient.Animal Studies: Manuscripts reporting research involving animals must include a statement that either the protocol was approved by an institutional animal care board or that the animal care complied with the "Principles of Laboratory Care" (formulated by the National Society for Medical Research) or the "Guide for the Care and Use of Laboratory Animals" (National Institutes of Health).
Funding Source: All manuscripts must include (on the title page) a statement of the source of funding of the study (if applicable). This information will appear as a footnote on the first page of the article.US National Institutes of Health (NIH) "Public Access Policy":For works that have received NIH funding (confirmed by NIHgrant number), Elsevier will deposit to PubMed Central (PMC) thefinal peer-reviewed accepted manuscripts on behalf of PM&Rauthors. This service will help authors comply with the NIH policythat requires NIH-funded authors submit to PubMed Central(PMC), or have submitted on their behalf, their peer-reviewedauthor manuscripts, to appear on PMC no later than 12 monthsafter final publication.
Device Status: A statement (appearing on the title page of the manuscript) regarding the presence or absence of the use of any medical devices in the study is required. A notation will appear as a footnote on the first page of the article. If a medical device(s) is discussed, then a statement regarding its legal/regulatory status is required including FDA status (e.g. approved for indicated use, investigational, exempt from regulations (and why), not approved, or unknown).SUBMISSION CATEGORIES
The content of PM&R includes articles that are contemporary and important to research, clinical practice, and education and training. The corresponding author will be required to identify for which category the manuscript is submitted. Each category has different submission requirements in terms of style, length and format. Please review the specific submission category sections for detailed submission information. Manuscripts that do not adhere to the following instructions may be returned to the corresponding author for technical revision before undergoing peer review.Unsolicited submissions that will be considered for peer review:
Basic science and clinical research including observational prospective or retrospective cohort studies, randomized and nonrandomized clinical trials, cost-effectiveness studies and clinically relevant translational science. The manuscript text should be limited to 5,000 words excluding references, tables and figures, which should be used when necessary to extend the understanding of the text. All original research manuscripts must be accompanied by a structured abstract of no more than 300 words that is described in detail below (see Manuscript Preparation). The text should include the following sections: introduction, methods (subjects, procedures, outcome measures, etc.), results (including reporting of statistical analysis with text as well as supplemental tables and figures), discussion (including interpretation of findings, clinical impact and applicability of results, and strengths and weaknesses of the study) and conclusion.
Case presentationsPM&R has instituted a formal policy regarding the publication of case reports or case series in which each subject's information is described individually. It is a requirement that formal, written permission be secured from the patient(s)/subject(s) of case reports or case series before publication. The purpose of this "informed permission" is to educate the subjects of such case reports regarding the nature of disseminating their personal health information, ensuring maximal deidentification and anonymity, and allowing the subject(s) the option of declining such release of information. It is expected that requesting such informed permission from these subjects should actually enhance their trust and respect for the process, thus facilitating their approval.
A case study or case series reporting on a new or unusual syndrome or medical condition, new diagnostic method, or highlight of an important clinical complication of a common condition. The manuscript should be limited to 1,500 words excluding references, tables and figures. The text should include the following sections: introduction, presentation of the case report or series, and discussion. For Case Reports, a brief, unstructured abstract (not to exceed 100 words) should be included. References should be limited to 10 (ten) and at least one figure should be included, but a maximum of two figures allowed.
You are required to engage in a reasonable effort to locate the subject(s) of your case report and discuss this informed permission form with him/her/them directly. Once this form is completed and permission granted (by signature), you are advised to safely retain this form as part of your records, with the understanding that it should be made available to the editor-in-chief or managing editor on request. It is understood that situations will arise in which it is not possible to obtain informed permission from a subject, ie, the subject is deceased, the subject has moved and is not trackable, the subject has a disability that prevents adequate comprehension of the informed permission request. If a legal surrogate or guardian (family member or otherwise) is identified, then this person is allowed to supply the informed permission. If after due diligence, neither the subject or legal surrogate, guardian, or family member is found or identified, then the case report may be submitted without obtaining informed permission. The cover letter accompanying your manuscript submission should stipulate whether or not informed permission was obtained.If your institution already requires completion of a similar Patient Consent form, we request that a copy of the blank form be sent to us so that we can ensure it is a suitable substitute.
Your cooperation with this policy is appreciated. Form can be downloaded from http://ees.elsevier.com/pmrjournal.
- There are 2 main review article types: Narrative and Analytical.Each can be written in a focused or comprehensive format.
A Narrative Review Includes:An Analytical Review Includes:
• Non-structured abstract (maximum 250 words)
• Introduction (including a statement of purpose)
• Describe method of literature selection including inclusion andexclusion criteria
• Summary of published literature ("evidence")
• Review may be chronological, conceptual, or thematic
• Tables and figures useful to present data
• Summary stating the conclusion(s) of the review includingclinical applicability
• Subject matter that is historically relevant, contemporary, orcutting edge
• Can be focused or comprehensive
• Focused: limited to 3,500 words excluding references (generallyup to 50), and tables and figures (generally up to 4)
• Comprehensive: limited to 7,500 words, excluding references,tables, and figures
• Structured abstract
- Objective: state the primary objective of the review article.
- Type: see subtypes below
- Literature Survey: include data sources, constraints, and timeparameters
- Methodology: summarize data extraction and analysis
- Synthesis: describe the main results
- Conclusions: state primary conclusion(s) and clinical applicability.
• Introduction (including a statement of purpose)
• Detailed description of methodology (including search criteria)
• In depth assessment of published literature ("evidence")
• Emphasis on appraisal of quality, synthesis of information, andanalysis/comparison of results or conclusions (based on subtype)
• Summary stating conclusion(s) of the review including clinicalapplicability
• Subject matter that is contemporary or cutting edge
• Can be focused or comprehensive
• Focused: limited to 3,500 words excluding references (generallyup to 50), and tables and figures (generally up to 4)
• Comprehensive: limited to 7,500 words, excluding references,tables and figures
Subtypes of Analytical Reviews:Systematic Review: Uses explicit methods to search, appraise,and synthesize research evidence in order to address a specificstudy question. The guidelines provided by the Cochrane Collaborationor the NHS Centre for Reviews and Dissemination areoften followed, particularly grading of strength (quality) of evidence.The process is transparent in the reporting of its methods tofacilitate others to replicate the process. Systematic reviews seek todraw together all available knowledge on a topic area, requiring anexhaustive, comprehensive literature search. The analysis leads toa determination of what is known and unknown about the studyquestion, and leads to recommendations for future research.
Critical Review: Presents, analyzes, and synthesizes materialfrom diverse sources. The emphasis is on the conceptual contributionof each item of included literature, not on formal qualityassessment. While such a review does serve to aggregate theliterature on a topic, there is no formal requirement to explicitlypresent methods of the search, synthesis, and analysis. Criticalreviews typically result in a hypothesis or a model, not an answer.The resultant model may be a synthesis of existing schools ofthought or it may be a completely new interpretation of theexisting data.Systematic Search and Review: Combines the strengths of acritical review (see previous) with a comprehensive search process.Typically, this type of review addresses broad questions, andthe result is a best evidence synthesis. The broad scope of this typeof review means that it often incorporates multiple study typesrather than focusing on a single preferred study design, thusproviding a much more complete picture of the prevalence ofresearch on a topic than a systematic review limited to randomizedcontrolled trials. Subjecting the resultant literature to critical reviewor critique, albeit informally without the use of a standardizedtool or checklist, provides a useful evaluative component.However, this presupposes that all included articles are beingassessed and valued against the same underlying criteria, a factthat cannot usually be determined from the review's methodology.
Meta-Analysis: A technique that statistically combines the results of quantitative studies to provide a more precise effect of the results. A good systematic review is essential to a meta-analysis of the literature. For a meta-analysis to be valid requires all included studies to be sufficiently similar; this includes characteristics such as the study population, intervention, and comparison(s) being made. Most importantly, it requires that the same measure or outcome be assessed in the same way and at the same time intervals. Reporting of meta-analyses should conform to the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) Statement criteria. These are available at http://www.prisma-statement.org/.Mixed studies review/mixed methods: Any combination of methods where at least one of the components is usually a systematic review. It most frequently refers to the bringing together of a qualitative review (conceptual) and a quantitative analysis (practical). Such reviews attempt to bring the evidence of "what works"together with the theoretical of "how and why does it work" to start to address the more complex issue of "what works underwhich circumstances." This review type seeks correlations between practical and theoretical and uses gap analysis to identifyaspects absent in the literature. Mixed methods reviews provide a potentially more complete picture of the research landscape in a specific topic area.[Review Format definitions used/modified with permission from Grant MJ, Booth A. A typology of reviews: an analysis of the 14review article types and associated methodologies. Health Information and Libraries Journal 2009;26:91-108. Available at: http://onlinelibrary.wiley.com/doi/10.1111/j.1471-1842.2009.00848.x/full. Accessed April 17, 2012.]
- Clinical pearls
A brief vignette describing a new or unique diagnostic or treatment method for a specific medical condition or category that would have relevance to the average physiatrist or practitioner in another rehabilitation discipline. This should include a short review of the history of previous methods, a description of the new method, and justification for the basis of the new approach. The Clinical Pearls do not have to be presented with a specific case. These manuscripts should be no more than 1,000 words (excluding references) with no more than two figures or tables.
A short technical report of a new or emerging technology, treatment or device, with relevance to the field of physical medicine and rehabilitation. These manuscripts should be no longer than 750 words (excluding references) with a limit of one figure or table.
A column presenting images (e.g. radiographs, CT, MRI, electrodiagnostic tracings, pathology, physical examination findings) that are unique, interesting, pertinent and relevant to the understanding of health and disease in the field of physical medicine and rehabilitation. All images should be accompanied by a short description of the image and relevant relationship to clinical care or research science of no more than 500 words (excluding references) with references limited to 5 (five).
Letters to the editor are encouraged and will be considered for publication at the Editor-in-Chief's discretion. All letters should be brief (no more than 750 words) and relate to the specific article being commented on. Letters should not reference any unpublished literature and references are limited to no more than 5 (five). Letters are also subject to editorial modification.
Articles Solicited by Editor-in-Chief and Senior Editors only:
A debate format of a specific question, usually based on a controversial therapeutic intervention, but could include a theoretical dilemma, diagnostic uncertainty, or other topic in physical medicine and rehabilitation, through which two parties with legitimate opposing perspectives present arguments to support their viewpoints. This column allows more editorial freedom than a critical review, but the basis of these viewpoints should include scientifically sound arguments supported by available medical evidence as well as personal experience and perspective. Each of the two portions of the manuscript should be no greater than 1,500 words (excluding references) with references limited to no more than 15 (fifteen). No abstract is required, but a brief introduction stating the writer's viewpoint should be included as part of the text. Figures and tables are not required.Practice management
A column that focuses on a contemporary issue in clinical physiatric practice relating to health policy, business and/or medical issues such as coding and billing, practice innovations, and new trends in physiatric education/training after residency/fellowship. Manuscripts should be no more than 2,500 words and include an introduction, presentation of the main issue(s) including a comprehensive discussion of clinical implications, and a brief conclusion. There should be no more than 15 (fifteen) references and figures or tables should be limited to two.
Ethical-legal topicsInvited Perspective
An in-depth assessment of a specific topic in physical medicine and rehabilitation that raises questions and concerns across the medical, ethical and legal fields. Depending on the topic, the column may include either, or both, an ethical and legal perspective which provides the reader with a unique or new perspective on the subject. (If both a legal and ethical piece are presented, these may represent convergent or divergent ideas). The total word count for this column is 3,000 words, with each of the two portions of the manuscript no greater than 1,500 words (excluding references) with references limited to no more than 15 (fifteen). No abstract is required, but a brief introduction stating the purpose of the discussion should be included as part of the text. Figures and tables are not required.
Invited commentaries or viewpoints on contemporary topics in the field of physical medicine and rehabilitation featuring medical diagnosis and treatment, educational and medical training, socioeconomic factors and others topics. These are usually solicited from experts and leaders in the field and are designed educate and stimulate thought and discussion. Perspective discusses current conditions and future expectations and authors may add personal insight and opinion. Manuscripts should be approximately 2,000 words. At the Editor-in-Chiefs discretion, unsolicited Perspective manuscripts will be considered for publication, but it is strongly suggested that potential authors contact the editorial office first.
International PerspectiveMANUSCRIPT PREPARATION
Invited descriptions, viewpoints, or reviews on contemporary topics of international relevance to the field of physical medicine and rehabilitation. It focuses on areas of scientific and clinical relevance for the advancement of rehabilitation in an international context. Articles can present and discuss current practice, emerging issues, or trends and developments from a specific part of the world. Other topics of broad international relevance are also considered. These are usually solicited from experts and leaders in the field, and authors may add personal insight and opinion. Manuscripts should be approximately 2,500 words. At the Editor-in-Chiefs discretion, unsolicited manuscripts will be considered for publication, but it is strongly suggested that potential authors contact the editorial office first.
These instructions generally follow the Uniform Requirements for Manuscripts Submitted to Biomedical Journals (N Engl J Med 1997; 336:309 or see http://www.icmje.org/index.html ). Once accepted, manuscripts are copy edited to conform to the Journal's standards and style.Format
The preferred word processing program is Microsoft Word. Manuscripts should be double-spaced throughout (including tables, references, and figure legends), and have at least 3 cm margins. The text should be ragged right (no right justification). Embedded instructions (eg, italics, underlines, boldface) should not be used or kept to a minimum. Do not use coding for centering. Insert only one space after punctuation marks. Sequential page numbering should begin with the abstract. The order of sections is Abstract, Text, Acknowledgments, References, Tables, and Figure Legends. To ensure blinded peer-review, no direct references to the author(s) or institution of origin should be made anywhere in the text or figures. To facilitate peer review, please add line numbers to the document.
Title PageStructured Abstracts
The first page of your manuscript should be a blind title page. As a separate document, include a title page listing all authors' full names, highest academic degrees, and affiliations; name and address for correspondence, including fax number, telephone number, and e-mail address; and whether the material was presented at an AAPM&R Annual Assembly. Indicate any funding source and provide grant numbers for NIH funding.
The structured abstract is necessary for original research and analytical review articles. The structured abstract should be no more than 300 words, appear on the page following the title page, and use the following headings and information:
For Original Research Articles:Objective: State the main question or objective of the study and the major hypothesis tested, if any.
Design: Describe the design of the study, indicating, as appropriate, use of randomization, blinding, criterion standards for diagnostic tests, temporal direction (retrospective or prospective), and so on.Setting: Indicate the study setting, including the level of clinical care (e.g., primary or tertiary, private practice or institutional).
Patients (or Participants): State selection procedures, entry criteria, and numbers of participants entering and finishing the study.Methods or Interventions (or Assessment of Risk Factors): Describe essential features of any interventions, including their method and duration of administration. For observational studies, clearly outline the independent variables.
Main Outcome Measurements: The primary study outcome measures (dependent variables) should be indicated as planned before data collection began. If the hypothesis being reported was formulated during or after data collection, this fact should be clearly stated.Results: Report the main findings of the study.
Conclusions: State only those conclusions of the study that are directly supported by data, along with their clinical application (avoiding overgeneralization) or whether additional study is required before the information should be used in usual clinical settings.Acknowledgments
On a separate page, list any significant contributors to the conduct of the study or preparation of the manuscript other than your co-authors. Authors are responsible for obtaining permission from persons acknowledged for reasons other than technical, secretarial, or financial support.
StyleLaboratory slang and clinical jargon should be avoided. Keep unique abbreviations to a minimum. Spell out the full term for each abbreviation at first use in the text unless it is a standard unit of measure.
Follow the American Medical Association (AMA) Manual of Style, 10th edition. Stedman's Medical Dictionary (27th edition) and Merriam Webster's Collegiate Dictionary (10th edition) should be used as standard references. Use nonproprietary names of drugs, devices, and other products, unless the specific trade name of a drug is essential to the discussion. Capitalize trade names and place them in parentheses after the generic names. Include the name and location (city and state in USA; city and country outside USA.) of the manufacturer of any drug, supply, or equipment mentioned in the manuscript. Use the metric system to express units of measure and degrees Celsius to express temperatures, and use SI units rather than conventional units.
ReferencesFor journal articles with six or fewer authors, list surnames and initials of all authors. If there are more than seven authors, name only the first three authors and then use et al. Refer to the List of Journals Indexed in Index Medicus for abbreviations of journal names, or access the list at http://www.nlm.nih.gov/tsd/serials/lji.html . Sample references are given below:
The authors are responsible for the accuracy of the references. Key the references (double spaced) at the end of the manuscript. They should be cited in the text in the order of appearance. Cite unpublished data, such as papers submitted but not yet accepted for publication or personal communications, in parentheses in the text.
- Journal article 1. Cup EH, Pieterse AJ, ten Broek-Pastoor JM, et al. Exercise therapy and other types of physical therapy for patients with neuromuscular diseases: A systematic review. Arch Phys Med Rehabil 2007; 88:1452-1464.
Book chapter2. Leonard JA, Meier RH. Upper and lower extremity prosthetics. In: Delisa JA, Gans BM, eds. Rehabilitation Medicine Principles and Practice. Philadelphia, PA: JP Lippincott; 1998, 669-696.
Entire book3. Stewart JD, ed. Focal Peripheral Neuropathies. 3rd ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2000.
Online journal4. Tsao CC, Mirbagheri MM. Upper limb impairments associated with spasticity in neurological disorders. Journal of NeuroEngineering and Rehabilitation 2007, 4:45 doi:10.1186/1743-0003-4-45. Available at http://www.jneuroengrehab.com/content/4/1/45 . Accessed December 27, 2007.
World Wide Web5. Madans, J. The definition and measurement of disability: the work of the Washington Group. Powerpoint presentation, November 2006. Available at http://www.cdc.gov/nchs/citygroup.htm . Accessed June 1, 2007.
If reference is made in the text to personal communication (oral or written) as a source of information, a signed statement is required from the source.
Create tables using the table creating and editing feature of your word processing software (eg, Word, WordPerfect). Do not use Excel or comparable spreadsheet programs. Group all tables at the end of the manuscript, or supply them together in a separate file. Number and cite tables consecutively in the text. Each table should start on a separate sheet, and include the table title, appropriate column heads, and explanatory legends (including definitions of any abbreviations used). Tables should supplement, rather than duplicate, the material in the text.Figures
Electronic art should be created/scanned and saved and submitted as either a TIFF (tagged image file format) or as an EPS (encapsulated postscript) file. Figures must be cited in the text and numbered in order of first mention. Make sure that the figure number is marked clearly on the figure or part of the electronic file name (i.e., Figure1.tif). Line art must have a resolution of at least 1200 dpi (dots per inch), and electronic photographs, radiographs, CT scans, and scanned images must have a resolution of at least 300 dpi. Images should be supplied at a size that approximates the final figure size in the print journal. If fonts are used in the artwork, they must be converted to paths or outlines or they must be embedded in the files. Color images must be created/scanned and saved and submitted as CMYK files. Please note that artwork generated from office suite programs such Corel Draw and MS Word and artwork downloaded from the Internet (JPEG or GIFF files) cannot be used. Color illustrations are published at the discretion of the editorial office without additional charge to authors.
Legends must be submitted for all figures. They should be brief and specific, and they should appear on a separate manuscript page after the references. Use scale markers in the image for electron micrographs, and indicate the type of stain used.
Corresponding authors will receive page proofs to check the copyedited and typeset article before publication. Portable document format (PDF) files of the typeset pages and support documents (e.g., reprint order form) will be sent to the corresponding author via e-mail. Complete instructions will be provided with the e-mail for downloading and printing the files and for faxing the corrected pages to the publisher. It is the author's responsibility to ensure that there are no errors in the proofs. Changes that have been made to conform to Journal style will stand if they do not alter the authors' meaning. Only the most critical changes to the accuracy of the content will be made. The publisher reserves the right to deny any changes that do not affect the accuracy of the content. Authors may be charged for alterations to the proofs beyond those required to correct errors or to answer queries. Proofs must be checked carefully and corrections returned within 48 hours of receipt, as requested in the email accompanying the page proofs.
ReprintsAdditional material only for electronic version
Authors will receive a reprint order form and a price list from the Publisher. Reprint requests should be faxed with the corrected proofs, if possible. Reprints are normally shipped 6 to 8 weeks after publication of the issue in which the item appears. Contact the firstname.lastname@example.org with questions regarding author reprint orders.
Under special circumstances, PM&R will allow publication of additional tables, figures, or text (e.g., Methodology, explanations of analysis, etc) in the electronic version of the published manuscript only. This material will not be included in the print version but a reference to it being available online will be present in the print version. The Editor would like to emphasize that such additional material will have to meet strict criteria to be included in the electronic version; such material may be used to complement the data in the printed version. If deemed by the authors or Editor as crucial to the interpretation of the manuscript, this material should be included as part of the printed version of the manuscript. Please mark clearly in the submitted manuscript that this is additional information to be published electronically. The electronic version should not be used as a repository for redundant or unnecessary data.
Video Clips for electronic version: We accept and encourage submission of video clips with accepted manuscripts, to be viewed in the online version of the article, but only if such images are pertinent and complementary to the manuscript, and nonoffensive.Supplementary movies or animation files should be provided in one of the formats listed below to ensure that the majority of potential users have the best chance of being able to access, view, or play the data both now and in the future. Recommended upper limit: for ease of download, the recommended upper limit for the size of a single file is 10 MB.
Formats for Movies and Animation
- MPEG (*.mpg): Preferred movie format; MPEG-1 or MPEG-2 format required; highest possible quality required.
- Apple QuickTime (*.mov): Acceptable movie format; highest possible quality required.
- Microsoft Audio/Video Interlaced format (*.avi): Acceptable movie format; highest possible quality required.
- Compuserve GIF (*.gif): Preferred format for animation of rasterized (pixel-based) images; highest possible quality required.
Rights and Permissions
Direct quotations, tables, or illustrations that have appeared in copyrighted material must be accompanied by written permission for their use from the copyright owner and original author along with complete information as to the source. Photographs of identifiable persons must be accompanied by signed releases, showing informed consent. Articles appear in both the printed and online versions of PM&R and wording of the release should specify permission in all forms and media. Failure to get electronic permission rights may result in the images not appearing in the online version.May 2012
- (1) Patent and trademark rights to any process or procedure described in the article;