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Author Instructions

Clinical Clinical observation refers to records of 2000 Unstructured abstract. 3-8 The main content should
Observation the effects of treatment on hospitalized max No more than 250 words. keywords include four sections:
patients. It details symptoms, diagnosis Introduction, Methods,
and treatment of the disease to be Results and Discussion.
reported. The characteristics of clinical
reports include new or rare, complex
adverse reactions, confusing symptoms
or signs, examples of new theories, etc.

Brief Brief communications are timely, peer- 1500 Unstructured abstract. 3-6 The brief
Communication reviewed, and short (2-4 journal pages). max No more than 150 words. keywords communication is a
These may be used to report new one body text with
developments, significant advances, maximum 4 items
and novel aspects of experimental and (figures and tables) and
theoretical methods and techniques 12 references.
which are relevant for scientific
investigations within the journal scope.

2.3 Manuscript Structure
2.3.1 Front Matter
2.3.1.1 Title
The title of the manuscript should be concise, specific and relevant, with no more than 16 words if possible. When gene or
protein names are included, the abbreviated name rather than full name should be used.

2.3.1.2 Authors and Affiliations
Authors’ full names should be listed. The initials of middle names can be provided. Institutional addresses and email
addresses for all authors should be listed. At least one author should be designated as corresponding author. In addition,
corresponding authors are suggested to provide their Open Researcher and Contributor ID upon submission. Please note
that any change to authorship is not allowed after manuscript acceptance.

2.3.1.3 Abstract
Original research, systematic reviews, and meta-analyses require structured abstracts. The abstract should provide the
context or background for the study and should state the study’s purpose, basic procedures (selection of study participants,
settings, measurements, analytical methods), main findings (giving specific effect sizes and their statistical and clinical
significance, if possible), and principal conclusions. It should emphasize new and important aspects of the study or
observations, note important limitations, and not overinterpret findings. Clinical trial abstracts should include items that the
CONSORT group has identified as essential. It is not allowed to contain results which are not presented and substantiated in
the manuscript, or exaggerate the main conclusions. Citations should not be included in the abstract.

2.3.1.4 Keywords
Three to eight keywords should be provided, which are specific to the article, yet reasonably common within the subject
discipline.
2.3.2 Main Text
Manuscripts of different types are structured with different sections of content. Please refer to Types of Manuscripts to
make sure which sections should be included in the manuscripts.

2.3.2.1 Introduction
The introduction should contain background that puts the manuscript into context, allow readers to understand why the
study is important, include a brief review of key literature, and conclude with a brief statement of the overall aim of the
work and a comment about whether that aim was achieved. Relevant controversies or disagreements in the field should be
introduced as well.

2.3.2.2 Methods
Methods should contain sufficient details to allow others to fully replicate the study. New methods and protocols should be
described in detail while well-established methods can be briefly described or appropriately cited. Experimental participants
selected, the drugs and chemicals used, the statistical methods taken, and the computer software used should be identified
precisely. Statistical terms, abbreviations, and all symbols used should be defined clearly. Protocol documents for clinical
trials, observational studies, and other non-laboratory investigations may be uploaded as supplementary materials.
VII Ageing and Neurodegenerative Diseases