Haemophilia Template
Write in a clean editor, then format for Haemophilia in one click — DocuGuru applies the official Wiley template with author–year references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.
About the Haemophilia format
Haemophilia is a peer-reviewed journal published by Wiley, covering Hemophilia Treatment and Research, Platelet Disorders and Treatments, Blood Coagulation and Thrombosis Mechanisms.
| Publisher | Wiley |
|---|---|
| Reference style | Author–year (Chicago) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Haemophilia 12 (3): 45–58.
Formats any DOI in Haemophilia style. No sign-up. |
| Publishes research in | Hemophilia Treatment and Research Platelet Disorders and Treatments Blood Coagulation and Thrombosis Mechanisms Coagulation, Bradykinin, Polyphosphates, and Angioedema Hemostasis and retained surgical items |
| ISSN | 1351-8216 |
| Citation impact (2-yr) | 2.06 |
| h-index | 123 |
| i10-index | 3,458 |
| Total citations | 145,640 |
| Article processing charge | $4,530 |
| Top institutions publishing here | University College London |
| Journal website | onlinelibrary.wiley.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Haemophilia per year
Citation impact of Haemophilia by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in Haemophilia
Hemophilia is a rare disorder that is complex to diagnose and to manage. These evidence-based guidelines offer practical recommendations on the diagnosis and general management of hemophilia, as well as the management of complications including musculoskeletal issues, inhibitors, and transfusion-transmitted infections. By compiling these guidelines, the World Federation of Hemophilia aims to assist healthcare providers…
von Willebrand disease (VWD) is a commonly encountered inherited bleeding disorder affecting both males and females, causing mucous membrane and skin bleeding symptoms, and bleeding with surgical or other haemostatic challenges. VWD may be disproportionately symptomatic in women of child-bearing age. It may also occur less frequently as an acquired disorder (acquired von Willebrand syndrome).…
The rare coagulation disorders are heritable abnormalities of haemostasis that may present significant difficulties in diagnosis and management. This review summarizes the current literature for disorders of fibrinogen, and deficiencies of prothrombin, factor V, FV + VIII, FVII, FX, the combined vitamin K-dependent factors, FXI and FXIII. Based on both collective clinical experience and the…
Many diseases and injuries can impair joint mobility. Normal reference values are needed to determine extent of impairment to assess and monitor joint motion. There is very little published data describing normal joint range of motion (ROM) for healthy men and women across a wide span of ages. We enrolled male and female subjects aged…