4 天之前 · Every year BMJ Case Reports selects authors of global health case reports to join our editorial team as a global health associate editor. This is an opportunity to gain some editorial experience or join our team on research and educational projects.

All submissions to BMJ Case Reports require the completion of author statements. At least one of the co-authors should be the lead clinician responsible for the patient’s care and responsible for the integrity of the content of the case report, signed informed consent and author statements accompanying each manuscript.

A journal publishing case reports in all medical disciplines, including general medicine, drug interaction and adverse reactions. The largest online collection of medical case reports.

BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.

Early intrathecal dexamethasone (IT-Dexa) associated with faster recovery and good outcome in an adolescent with febrile infection-related epilepsy syndrome (FIRES) (3 February, 2025)

Leflunomide-induced drug reaction eosinophilia systemic symptoms and haemophagocytic lymphohistiocytosis overlap syndrome with rheumatoid arthritis (29 January, 2025 ...

2025年1月29日 · Lone Bak Posada, Anne Estrup Olesen, Tine Høg Sørensen, Samuel Azuz

Concurrent existence of cold agglutinin disease and ANCA-associated vasculitis with fulminant pulmonary-renal syndrome poses significant treatment challenges (29 July, 2024)

Management dilemma of a peri-prosthetic intracapsular neck of femur fracture in a young patient: Importance of biomechanical considerations when weighing up decision to mobilise, fix or replace (27 December, 2024)

Barth syndrome (BTHS) is one of the rare X linked recessive diseases that appear in infancy with a triad of myocardial and skeletal muscle diseases, neutropenia and growth retardation. The pathogenic variant of TAFAZZIN gene leads to BTHS, which encodes the TAFAZZIN protein of the inner membrane of the mitochondria, a phosphatidyltransferase involved in cardiolipin remodelling and functional ...