Guide for Authors
Best Practice & Research Clinical Haematology publishes review articles integrating the results from
the latest original research articles into practical, evidence-based review articles. These articles seek to address the key clinical
issues of diagnosis, treatment and patient management. Each issue follows a problem-orientated approach which focuses on the key questions
to be addressed, clearly defining what is known and not known, covering the spectrum of clinical and laboratory haematological practice
and research. Although most reviews are invited, the Editor welcomes suggestions from potential authors. They should first write an outline
of the intended review and send this to:
Dr Jacob M. Rowe
Chief, Department of Hematology and Bone Marrow Transplant
Rambam Medical Centre
Haifa 31096
Israel
Fax: +972 4854 2343 Email: rowe@jimmy.harvard.edu
1.
Authorship
All authors should have made substantial contributions to all of the following: (1) 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 submitted.
2. Acknowledgements
All contributors who do not meet the criteria for authorship as defined
above should be listed in an acknowledgements section. Examples of those who might be acknowledged include a person who provided purely
technical help, writing assistance, or a department chair who provided only general support. Authors should disclose whether they had
any writing assistance and identify the entity that paid for this assistance.
3. Conflict of interest
At the end of the
text, under a subheading "Conflict of interest statement" all authors must disclose any financial and personal relationships
with other people or organisations that could inappropriately influence (bias) their work. Examples of potential conflicts of interest
include employment, consultancies, stock ownership, honoraria, paid expert testimony, patent applications/registrations, and grants or
other funding.
4. Role of the funding source
All sources of funding should be declared as an acknowledgement at the
end of the text. Authors should declare the role of study sponsors, if any, in the collection, analysis and interpretation of data and
in the writing of the manuscript. If the study sponsors had no such involvement, the authors should so state.
Changes to Authorship
This policy concerns the addition, deletion, or rearrangement of author names in the authorship of accepted manuscripts:
Before the
accepted manuscript is published in an online issue: Requests to add or remove an author, or to rearrange the author names, must be sent
to the Journal Manager from the corresponding author of the accepted manuscript and must include: (a) the reason the name should be added
or removed, or the author names rearranged and (b) written confirmation (e-mail, fax, letter) from all authors that they agree with the
addition, removal or rearrangement. In the case of addition or removal of authors, this includes confirmation from the author being added
or removed. Requests that are not sent by the corresponding author will be forwarded by the Journal Manager to the corresponding author,
who must follow the procedure as described above. Note that: (1) Journal Managers will inform the Journal Editors of any such requests
and (2) publication of the accepted manuscript in an online issue is suspended until authorship has been agreed.
After the accepted
manuscript is published in an online issue: Any requests to add, delete, or rearrange author names in an article published in an online
issue will follow the same policies as noted above and result in a corrigendum.
5. Copyright
Upon acceptance of an article,
authors will be asked to sign a "Journal Publishing Agreement" (for more information on this and copyright see
http://www.elsevier.com/wps/find/supportfaq.cws_home/copyright).
Acceptance of the agreement will ensure the widest possible dissemination of information. An e-mail (or letter) will be sent to the corresponding
author confirming receipt of the manuscript together with a "Journal Publishing Agreement" form.
If excerpts from other
copyrighted works are included, the author(s) must obtain written permission from the copyright owners and credit the source(s) in the
article. Elsevier has preprinted forms for use by authors in these cases : contact Elsevier's Rights Department, Philadelphia, PA, USA:
Tel. (+1) 215 238 7869; Fax (+1) 215 238 2239; e-mail healthpermissions@elsevier.com . Requests may also be completed
online via the Elsevier homepage (
http://www.elsevier.com/locate/permissions).
6. Funding body agreements and policies
Elsevier has established agreements and developed policies to allow authors who publish in Elsevier journals to comply with potential
manuscript archiving requirements as specified as conditions of their grant awards. To learn more about existing agreements and policies
please visit
http://www.elsevier.com/fundingbodies
7. Proofs
One set of page proofs in PDF format will be
sent by e-mail to the corresponding author (if we do not have an e-mail address then paper proofs will be sent by post). Elsevier now
sends PDF proofs which can be annotated; for this you will need to download Adobe Reader version 7 available free from:
http://www.adobe.com/products/acrobat/readstep2.html.
Instructions on how to annotate PDF files will accompany the proofs. The exact system requirements are given at the Adobe site:
http://www.adobe.com/products/acrobat/acrrsystemreqs.html#70win. If you do not wish to use the PDF annotations function, you may list the corrections (including replies to the Query Form) and return
to Elsevier in an e-mail. Please list your corrections quoting line number. If, for any reason, this is not possible, then mark the corrections
and any other comments (including replies to the Query Form) on a printout of your proof and return by fax, or scan the pages and e-mail,
or by post.
Please use this proof only for checking the typesetting, editing, completeness and correctness of the text, tables and
figures. Significant changes to the article as accepted for publication will only be considered at this stage with permission from the
Editor. We will do everything possible to get your article published quickly and accurately. Therefore, it is important to ensure that
all of your corrections are sent back to us in one communication: please check carefully before replying, as inclusion of any subsequent
corrections cannot be guaranteed. Proofreading is solely your responsibility. Note that Elsevier may proceed with the publication of
your article if no response is received.
8. Offprints
The Corresponding author, at no cost, will be provided with a PDF
file of the article via e-mail. The PDF file is a watermarked version of the published article and includes a cover sheet with the journal
cover image and a disclaimer outlining the terms and conditions of use.
9. Ethics
Identifying information, including
patients' images, names, initials, or hospital numbers, should not be included in videos, recordings, written descriptions, photographs,
and pedigrees unless the information is essential for scientific purposes and you have obtained written informed consent for publication
in print and electronic form from the patient (or parent, guardian or next of kin where applicable). If such consent is made subject
to any conditions, Elsevier must be made aware of all such conditions. Written consents must be provided to Elsevier on request. Even
where consent has been given, identifying details should be omitted if they are not essential. If identifying characteristics are altered
to protect anonymity, such as in genetic pedigrees, authors should provide assurance that alterations do not distort scientific meaning
and editors should so note. If such consent has not been obtained, personal details of patients included in any part of the paper and
in any supplementary materials (including all illustrations and videos) must be removed before submission.
10. Randomised controlled
trials
All randomised controlled trials submitted for publication in Best Practice & Research Clinical Haematology should
include a completed Consolidated Standards of Reporting Trials (CONSORT) flow chart. Please refer to the CONSORT statement website at:
http://www.consort-statement.org for more information. Best Practice & Research Clinical Haematology has adopted the
proposal from the International Committee of Medical Journal Editors (ICMJE) which require, as a condition of consideration for publication
of clinical trials, registration in a public trials registry. Trials must register at or before the onset of patient enrolment. The clinical
trial registration number should be included at the end of the abstract of the article. For this purpose, a clinical trial is defined
as any research study that prospectively assigns human participants or groups of humans to one or more health-related interventions to
evaluate the effects of health outcomes. Health-related interventions include any intervention used to modify a biomedical or health-related
outcome (for example drugs, surgical procedures, devices, behavioural treatments, dietary interventions, and process-of-care changes).
Health outcomes include any biomedical or health-related measures obtained in patients or participants, including pharmacokinetic measures
and adverse events. Purely observational studies (those in which the assignment of the medical intervention is not at the discretion
of the investigator) will not require registration. Further information can be found at:
http://www.icmje.org. If a CONSORT
flow chart is not included with the submitted manuscript, authors should provide a statement explaining the omission.
11. Disclosure
of clinical trial results
In line with the position of the International Committee of Medical Journal Editors, Best Practice & Research Clinical Haematology is willing to consider manuscripts which include results posted in the same clinical trials registry
in which primary registration resides. It will not consider such postings to be prior publication, providing the results are presented
in the form of a brief structured (500 words) abstract or table. However, divulging results in other circumstances (eg, investors' meetings)
is strongly discouraged and may jeopardise consideration of the manuscript. Authors should fully disclose all postings in registries
of the same or closely related work.
FORMATTING INSTRUCTIONS
General Information: It is the responsibility of
the authors to write in standard, grammatical English. Spelling may be British or American, but must be consistent throughout the text,
tables and legends to tables and figures.
(a) Title Page: Identify the category of the communication on top of the page. Include
a brief and descriptive Title of the article, the full Name(s) of the Author(s)(in the format First Name, Initials, and Surname) and
the Name and Location of the institution where the research was carried out. A word count of the text should include Tables and Legends.
Exclude the Abstract and Reference list. The name, postal and email addresses, telephone and fax numbers of the corresponding author
should be included at the bottom of the title page as well as, if necessary, additional addresses of other Authors. If the manuscript
was presented at a meeting, the name of the organization, the place and the date on which it was read must be indicated.
(b) Abstract
Page: Abstracts are required for original articles only. The abstract is essential and the most read part of the paper. It should
be informative, not descriptive, and should avoid abbreviations except for units of measure. An abstract for a regular article should
not exceed 250 words and should end with the principal conclusions of the study. Structured abstracts are encouraged and should use the
following headings: Introduction, Materials and Methods, Results and Conclusions.
Keywords and Abbreviations should follow
the abstract and be on the same page (or on a separate page if no abstract). List up to 6 key words for subject indexing, preferably
to be taken from Index Medicus. List all abbreviations used.
(c) Text of Articles: The text should be arranged as follows: Introduction, without heading, should state the purpose of the investigation and give a short review of pertinent literature.
Materials and methods should be described in detail with appropriate information about patients or experimental animals.
Authors should stipulate that informed consent was obtained when applicable to research on humans, with the comment that the
study was approved by the institutional Ethics Committee on human research. Manuscripts reporting animal experiments must include
the statement that all animals received care in compliance with the American, European, or any other Convention on Animal Care, with
the comment that the study was approved by the institutional Ethics Committee. Generic names of drugs and equipment should be used throughout
the manuscript with brand names (proprietary name) and the name and location (city, state, country) of the manufacturer in parentheses
when first mentioned in the text.
Results should be reported concisely. Results presented either in tables or figures should
be commented on in the text.
Discussion is an interpretation of the results and their significance with reference to pertinent
work by other authors. It should be clear and concise. The importance of the study and its limitations should be discussed.
Acknowledgments
of financial or personal assistance should be placed at the end of the text.
(d) References: Consecutive numbers in square
brackets should be used to indicate references in the text, e.g., [1,2], as part of the text and not raised above it.
The full reference
should be cited in a numbered list essentially according to the Vancouver Uniform Requirements (5th ed., Ann Intern Med 1997;126(1):36-47).
References should contain names of the first yhree authors (surnames first followed by initials), Title of communication in lower case
lettering, Title of Journal [abbreviated according to International Serials Data System-List of Serial title Word Abbreviations, 1985
(ISDS-ISO International Centre, 20 rue Bachaumont, 75002 Paris, France)], year of publication; volume number: first and last page number
(see Ref.1).
Reference to Journal Supplement, cf. example (Ref. 2).
References to books should contain Author Name(s) in the
same format as above: Title. Publisher's location: Name; Year of publication. page range (see Ref. 3).
References to multi-author
books with editor(s) should contain Author Name(s) in the same format as above: Title of contribution. In: Name(s) of editor(s). Title
of book. Publisher's location: Name; Year of publication. If necessary page range (see Ref. 4)
For communications which have been
accepted for publication, but not yet printed, the reference must contain the journal name and year (see Ref. 5). Material referred to
by the phrase "personal communication" or "submitted for publication" are not considered full references and should
only be placed in parentheses at the appropriate place in the text, e.g., (Hessel 1997 personal communication).
Examples of references
are shown below.
1. Ordljin TM, Shainoff JR, Lawrence SO. Thrombin cleavage enhances exposure of heparin binding domain in the N-terminus
of the fibrin beta chain. Blood 1996;88:2050-61.
2. Copley AL. The endoendothelial fibrin lining. Thromb Res 1983;(SV):1-154.
3. Davies JT, Rideal EK. Interfacial Phenomena. New York-London: Academic Press; 1961. p. 110-30.
4. Blomback B. Fibrinogen to fibrin
transformation. In: Seegers WH, editor.
Blood Clotting Enzymology. New York-London: Academic Press; 1967. p. 143-215.
5. Leshner
AI. Molecular mechanisms of cocaine addiction. N Engl J Med. In Press 1996.
(e) Tables and Figures: Tables and figures are
submitted via the online submission system EES with the accompanying article. Each Table should be included on a separate page. Tables
should supplement but not duplicate the text. A brief title should be provided for each. Abbreviations used in Tables should be defined.
Legends to Tables should be included at the end of the manuscript file. Figures should be in black and white, all details clear enough
to permit reproduction, and legible in the actual size in which they should be published. If the number of tables and/or figures is excessive,
the author(s) could be asked to eliminate some of them. Authors wishing to provide colour figures should ensure that the artwork is in
an acceptable format (TIFF, EPS, or MS Office files) and at the correct resolution. For more detailed specification on submitting electronic
illustrations, please see the following webpage: http://www.elsevier.com/locate/authorartwork
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