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期刊名:Oxford medical case reports

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ISSN:2053-8855

e-ISSN:2053-8855

IF/分区:0.6/Q3

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共收录本刊相关文章索引1852
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Michael Isaacs,Uzzal K Talukdar,Krishna Gokula et al. Michael Isaacs et al.
IgA Nephropathy (IgAN) is one of the most common causes of glomerulonephritis. Biopsy is necessary for definitive diagnosis, though due to variability in severity and progression patients may forego biopsy initially. However, certain clinic...
Elinor Barsh,Jacob Keeling,Changlee S Pang et al. Elinor Barsh et al.
Follicular lymphoma is an indolent B-cell non-Hodgkin lymphoma typically characterized by the t(14;18)(q32;q21) translocation resulting in B-cell lymphoma 2 (BCL2)/immunoglobulin heavy chain (IGH) fusion. Nontranslocation variants are rare ...
Byung K Lee,Jaime P Gastwirt Byung K Lee
Parkinson's Disease is on the rise over the coming decades with expectations that more patients will be prescribed levodopa therapy. This case presents a patient with Parkinson's Disease who presented with severe symptomatic microcytic anem...
Sumanth Srinivasa Shetty,Dhanushan Gnanendran,Lavinia Onos et al. Sumanth Srinivasa Shetty et al.
Background: Pancreatic pseudocyst fistulation into the portal venous system is rare. This may cause portal-vein thrombosis, portal hypertension, and biliary obstruction, complicating diagnosis and treatment. ...
Leon Schönfeld,Marko Stuhr,Lars Klinkert et al. Leon Schönfeld et al.
Background: Severe gout flares may rarely present as systemic inflammatory syndromes, closely mimicking sepsis. Milk-of-urate bullae are an uncommon manifestation of extensive crystal burden and are typically described in...
Khadija Belcadi Abassi,Karima Larbi Ouassou,Abdelilah Radi et al. Khadija Belcadi Abassi et al.
Von Willebrand disease (VWD) is the most common inherited coagulopathy, resulting from a deficiency of von Willebrand factor (VWF), which plays a central role in hemostasis. Type 3 VWD, the rarest and most severe form, is characterized by a...
Zack Bin Azlin,Selnan J Wuyep,Andreas K Demetriades Zack Bin Azlin
The reduced specificity of certain MRI findings for aggressive vertebral haemangiomas (VH) may result in uncertainty surrounding the diagnosis. Utilising concurrent CT scans in such cases may provide additional evidence to help improve diag...
Taha Yassine Aaboudech,Sabrine Derqaoui,Siham Mesmoudi et al. Taha Yassine Aaboudech et al.
Background: Cavitating Mesenteric Lymph Node Syndrome (CMLNS) is an uncommon complication of celiac disease, characterized by cystic mesenteric lymph nodes and high morbidity. ...