万维提示：
1、投稿方式：在线投稿。
2、期刊网址：
http://www.karger.com/Journal/Home/224215
3、投稿网址：
https://www.manuscriptmanager.net/NEO?product_id=224215
4、官网邮箱：neo@karger.com
5、官网电话：+41 61 306 1358
6、期刊刊期：一年出版8期。
2021年6月4日星期五
投稿须知【官网信息】
Neonatology
Author Guidelines
About the Journal
Aims and Scope
This highly respected and frequently cited journal is a prime source of information in the area of fetal and neonatal research. Original papers present research on all aspects of neonatology, fetal medicine and developmental biology. These papers encompass both basic science and clinical research including randomized trials, novel observational studies and epidemiology. Basic science research covers molecular biology, molecular genetics, physiology, biochemistry and pharmacology in fetal and neonatal life. In addition to the classic features the journal accepts papers for sections "Research Briefings", "Sources of Neonatal Medicine" (historical pieces) and "Global Neonatal Research". Papers reporting the results of animal studies should be based upon hypotheses that relate to developmental processes or disorders in the human fetus or neonate.
Journal Sections
Clinical Trials: Research Articles reporting on randomized clinical trials
Research Briefings: These are generally brief reports of proposed research of interest to our readership and could include shortened versions of trial protocols.
Sources of Neonatal Medicine: These are publications reporting historical aspects of the development of neonatology. They should follow the guidelines for Review Articles and the Editors-in-Chief would encourage potential authors to submit a 1-page summary of their proposed article prior to submission.
Novel Insights from Clinical Practice: Case Reports submitted to this section must present significant new insights or cases with an unusual or noteworthy course. The manuscript must include a statement that written informed consent for publication was obtained and from whom. The paper should have 2 boxes containing 1-2 bullet points each: “Established Facts” (what is already known) and “Novel Insights” (what new information this report provides).
Global Neonatal Research: This new section will consider manuscripts reporting research from authors working in low- or middle-income countries or regions. The types of paper that may be submitted include Research Articles, Review Articles, Brief Reports, and Case Reports.
Letters to the Editor: These should relate to articles recently published in Neonatology. Letters should be brief and to the point. If accepted the Editors-in-Chief reserve the right to allow the authors of the articles concerned to respond and if desired have this reply published alongside the letter to the editor.
Article Types
Research Article
Research Articles report on primary research. They must describe significant and original observations. Consideration for publication is based on the article’s originality, novelty, and scientific soundness, and the appropriateness of its analysis.
Research Articles are reports of original work. Authors are asked to follow the EQUATOR Network for Research Articles.
Prior approval from an Institutional Review Board (IRB) or an Ethics Review Committee is required for all investigations involving human subjects.
A downloadable template is available below.
Documents
Research Article (DOCX, 28.97 KB)
Research Articles should contain a 250-word structured abstract, a 2500-word text, a total of 4-6 figures or tables and approximately 25 key references. If necessary, supplementary material can be submitted for publication online.
Review Article
Review Articles are considered reviews of research or summary articles. They are state-of-the-art papers covering a current topic by experts in the field. They should give evidence on and provide answers to a well-defined aspect or question in a particular area. Review Articles must include a critical discussion of the reported data and give a clear conclusion with potential impacts on the standard of care.
A downloadable template is available below.
Documents
Review Article (DOCX, 23.75 KB)
The journal mostly commissions review articles but the Editors-in-Chief will consider suggestions for topics and authors upon receipt of a 1-page summary of the proposed review. Review Articles should contain a 250-word abstract, 3500-word text, up to 4 figures or tables and 35-40 key references.
Systematic Review
Systematic Reviews are literature reviews focused on a research question that synthesizes all high-quality research evidence relevant to that question. Systematic Reviews should be presented in the Introduction, Methods, Results, Discussion format. The subject must be clearly defined. The objective of a Systematic Review should be to arrive at an evidence-based conclusion. The Methods section should give a clear indication of the literature search strategy, data extraction procedure, grading of evidence, and kind of analysis used. We strongly encourage authors to comply with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.
A downloadable template is available below.
Documents
Systematic Review (DOCX, 27.56 KB)
Systematic Reviews should contain a 250 words abstract, 3500 words text with 4-6 figures and/or tables with 35 - 40 references. Supplementary material including extra references can be submitted for online publication.
Case Report
Case Reports can present a case study, case report, or other description of a case. Case Reports present significant new insights or cases with an unusual and noteworthy course. Submissions can be based on a case or a number of similar cases. The most important aspect of the presentation is that it should provide a new perspective on a recognized clinical scenario or may represent an entirely new clinical condition. The novelty of the case(s) may lie in the phenotype, the presentation, the investigation, and/or the management. We strongly encourage authors to comply with the CARE guidelines.The manuscript must include a statement detailing that written informed consent for publication was obtained and from whom (e.g. “Written informed consent was obtained from the patient for publication of this case report and any accompanying images.”). If the patient has died, consent for publication must be obtained from their next of kin. If the patient described in the case report is a minor or vulnerable, then consent for publication must be obtained from the parent/legal guardian. The completed consent form must be made available to the Editor if requested, and will be treated confidentially.
A downloadable template is available below.
Documents
Novel Insights (DOCX, 27.91 KB)
Authors may submit the following type of Case Report:
Novel Insights: This Case Report is to include highlighted boxes containing one or two bullet points on 'Established Facts' (what is already known) and 'Novel Insights' (what new information has been gained). These should be selected so as to reinforce the novelty of the clinical observation.
Case reports should contain a 150-word unstructured abstract, 1000-word text, 1-2 figures or tables and 5-10 references.
Brief Report
Brief Reports are short and/or rapid announcements of research results. They must contain data derived from cutting-edge research and be of potential interest to a large proportion of the readership. They are independent, concise reports representing a significant contribution to the field. Such communications should represent complete, original studies and should be arranged in the same way as full-length manuscripts with subheadings.
A downloadable template is available below.
Documents
Brief Report (DOCX, 27.12 KB)
Brief Reports should contain a 150-word structured abstract and a 1500 word body text with no more than 2 figures or tables and 10-15 references.
Letter
Letters may explore subjects related to matters discussed in the journal, providing the author’s perspective on a subject. Letters may discuss a recently published article and may lend support or constructively critique the article in line with the author’s experience. The editors reserve the right to share such letters to the authors of the article concerned prior to publication in order to permit response, ideally in the same issue of the journal. Letters should not include original data.
A downloadable template is available below.
Documents
Letter (DOCX, 24.24 KB)
Letters and responses should be no more than 500 words in length and contain no more than 1 figure or table, and 5 references.
Meta-Analysis
Works consisting of studies using a quantitative method of combining the results of independent studies (usually drawn from the published literature) and synthesizing summaries and conclusions which may be used to evaluate therapeutic effectiveness, plan new studies, etc. It is often an overview of clinical trials. We strongly encourage authors to comply with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.
A downloadable template is available below.
Documents
Meta-Analysis (DOCX, 26.7 KB)
Meta-Analysis should contain a 250-word abstract, 3500-word text, 4-6 figures or tables and 35-40 references. Supplementary material including extra references can be submitted for online publication.
Contact Information
Should you have any problems with your submission, please contact the editorial office:
Angela Lorenz
Editorial Office 'Neonatology'
S. Karger AG
P.O. Box
CH–4009 Basel (Switzerland)
Tel. +41 61 306 1358
Fax +41 61 306 1434
neo@karger.com
Editorial and Journal Policies
General Conditions
Only papers written in English are considered. The articles should be comprehensible to a reader who is fluent in English and should be edited prior to submission to ensure that standard English grammar and usage are observed. Use of a professional language editing service prior to submission can help avoid delays with the review process.
All manuscripts are subject to editorial review.
The presentation of manuscripts should follow the Uniform Requirements for Manuscripts Submitted to Biomedical Journals from the International Committee of Medical Journal Editors (ICMJE).
Karger journals aim to adhere to the COPE Code of Conduct and Best Practice Guidelines.
By submitting an article for publication, the authors agree to the transfer of the copyright to the publisher upon acceptance. Accepted papers become the permanent property of the Journal and may not be reproduced by any means, in whole or in part, without the written consent of the publisher.
The Submission Statement with original (hand-written) signatures is to be provided upon submitting the paper. If it is not possible to collect all signatures on a single document, individual copies should be provided for each author.
Karger recommends the use of original images and materials whenever possible. If a submitted manuscript contains third-party copyright material(s), it is the authors’ sole responsibility to obtain permission from the relevant copyright holder for reusing the material(s), including any associated licensing fee. The copyright and usage information needs to be checked carefully to avoid copyright infringement.
Most publishers offer a quick and easy way to clear permissions for their content via the built-in website application RightsLink or via https://www.copyright.com/get-permissions/. Another widely used licensing tool is PLSClear. Please check the publishers’ websites for the available options and user instructions.
Statements
All submitted manuscripts must contain a statements section after the main body of the text, but before the reference list.
Statement of Ethics
Published research must comply with internationally-accepted standards for research practice and reporting. Manuscripts may be rejected if the editors believe that the research has not been carried out within an appropriate ethical framework, and concerns raised after publication may lead to a correction, retraction, or expression of concern in line with COPE guidelines.
Studies involving human subjects (including research on identifiable human material and data) must have been performed with the approval of an appropriate ethics committee and with appropriate participants’ informed consent in compliance with the Helsinki Declaration.
In the manuscript, authors should specify the name of the ethics committee or other relevant authority who approved the study protocol and provide the reference number where appropriate. If ethics approval was not required, or if the study has been granted an exemption from requiring ethics approval, this should also be detailed in the manuscript (including the name of the ethics committee who made that decision).
For all research involving human subjects, written informed consent to participate in the study should be obtained from participants (or their parent/legal guardian where appropriate ) and a statement detailing this should appear in the manuscript. For studies involving vulnerable participants or participants at risk of potential coercion, detailed information regarding the steps taken to ensure informed consent must be provided. If consent was not obtained, please specify why and whether this was approved by the ethics committee.
In line with the ICMJE recommendations on the protection of research participants, authors must avoid providing identifying information unless strictly necessary for the submission and participants’ identifiable attributes must be anonymized in the manuscript and its supplementary files, if any. If identifying information is necessary, authors must confirm that the individual has provided written consent for the use of that information in a publication.
Research involving human embryonic stem cells, embryonic germ cells or induced pluripotent stem cells should comply with the ISSCR 'Guidelines for the Conduct of Human Embryonic Stem Cell Research' or an equivalent set of guidelines or applicable regulations.
Case Reports: Manuscripts reporting a case report must include a statement detailing that written informed consent for publication was obtained and from whom (e.g. “Written informed consent was obtained from the patient for publication of this case report and any accompanying images.”). If the patient has died, consent for publication must be obtained from their next of kin. If the patient described in the case report is a minor or vulnerable, then consent for publication must be obtained from the parent/legal guardian. The completed consent form must be made available to the Editor if requested, and will be treated confidentially.
Clinical Trials: In accordance with the ICMJE recommendations, all clinical trials should be registered in a publicly available registry approved by the WHO or ICMJE (see the list here) and the clinical trial number must be clearly stated in the manuscript. Manuscripts reporting clinical trials must adhere to the relevant reporting guidelines for their study design, such as CONSORT for randomized controlled trials, TREND for non-randomized trials, or other relevant reporting guidelines as detailed on the Equator network website.
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更多详情：
https://www.karger.com/Journal/Guidelines/224215
