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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:0.4/Q3

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共收录本刊相关文章索引1732
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
Mohammad Obada Alsadi,Dalia Alghali,Ayah Zoghpy et al. Mohammad Obada Alsadi et al.
Gougerot-Carteaud Syndrome (Confluent and Reticulate Papillomatosis, CARP) is a rare dermatological condition characterized by coalescent reticulate papules predominantly affecting the upper trunk and neck. The etiology remains debated, wit...
Mira Hallak,Baraa Emran,Fathi Milhem et al. Mira Hallak et al.
Anophthalmia is a rare congenital defect where no ocular tissue is seen, and it involves 1 out of 10 000 to 20 000 live births. It is largely part of syndromes and consists of genetic, environmental origins, or multifactorial causes. We pre...
Romina Garakani,Michael Moradi,Fatima Batool et al. Romina Garakani et al.
Merkel cell carcinoma (MCC) is a rare aggressive neuroendocrine malignancy that typically presents in the skin and rapidly progresses to other body parts. MCC is typically found in sun-exposed areas, mainly the head and neck region as well ...
Hongyu He,Hao Guo,Zhongtao Li et al. Hongyu He et al.
Background: The prevalence of diseases caused by parasites has decreased due to improved sanitary conditions. Acute pancreatitis caused by parasites, especially Ascaris lumbricoides worms, is relatively rare and difficult...
Maram Gad,Lanya Faiq,Emma Arifagic et al. Maram Gad et al.
Cogan Syndrome (CS) is a rare autoimmune disease, complicated by a variety of cardiac manifestations. This case report represents the only documented case in the Republic of Cyprus. It describes the experience of a 23- year-old woman with C...
Rova Malala Fandresena Randrianarisoa,Armel Mamihaja Andrianiaina,Mirantosoa Fabiola Ravelonjatovo et al. Rova Malala Fandresena Randrianarisoa et al.
We report a case of chromoblastomycosis presenting with osteolytic lesions in the foot of a 32-year-old man from Madagascar. Bone involvement occurred through contiguous spread several years after traumatic inoculation. The initial clinical...
Faiq I Gorial,Nabaa Ihsan Awadh,Sara S Khunda et al. Faiq I Gorial et al.
Glycogen storage disease type III (GSD III), or Cori disease, is a rare autosomal recessive disorder caused by a debranching enzyme deficiency, leading to abnormal glycogen accumulation. Clinical features include hepatomegaly, hypoglycemia,...
Ahmed Taha Ahmed Taha
Gastric and duodenal ulcer perforation represents one of the most critical causes of acute abdomen, necessitating urgent surgical intervention. While primary repair with omental patch remains the standard treatment for uncomplicated cases, ...
Ariel Ahl,Rafi Orphali,Kumar Desai Ariel Ahl
Rhabdomyolysis is a clinical syndrome characterized by the breakdown of skeletal muscle tissue, leading to the release of myoglobin and creatine kinase (CK) into the bloodstream. The condition clinically presents with myalgia, weakness, and...
Tahir Shahzad,Zain A Bhutta,Muhammad Abd Ur Rehman Tahir Shahzad
Ketamine use in the emergency department is more widespread than ever due to its favorable safety profile and combined analgesic and anesthetic properties. Its ability to stimulate the cardiovascular system via the sympathetic nervous syste...