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期刊名:Case reports in medicine

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ISSN:1687-9627

e-ISSN:1687-9635

IF/分区:0.8/N/A

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共收录本刊相关文章索引1617
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
Virtut Velmishi,Dritan Alushani,Ermira Dervishi et al. Virtut Velmishi et al.
Background: Duodenal atresia or stenosis are different degrees of the same abnormality. They usually occur at the level of the ampulla of Vater and are thought to be an embryologic defect during the development of the for...
Girma Deshimo,Haile Abebe,Getiye Damtew et al. Girma Deshimo et al.
Situs inversus totalis (SIT) is a rare medical condition characterized by a complete mirror-image reversal of the normal positioning of the internal organs. Aristotle initially described situs inversus in animals, while Fabricius first char...
Nikhil Aggarwal,Diletta Bianchini,Rosemeen Parkar et al. Nikhil Aggarwal et al.
Immune checkpoint inhibitors (ICI) are monoclonal antibodies that target immune checkpoint inhibitory receptors. They have revolutionised cancer treatment but can be associated with a wide range of adverse side effects. Rarely, they can be ...
Ahmad Rezaee Azandaryani,Amir Mohammad Salehi Ahmad Rezaee Azandaryani
Idiopathic hypertrophic pachymeningitis (IHP) is a rare disease with diffuse thickening of the dura mater that has no specific clinical symptoms and manifestations and it causes neurosurgeons to misdiagnose. A 4-year-old girl presented at t...
Qi Jin,Xinrui Zhang,Huifen Yang et al. Qi Jin et al.
We report a case of Klebsiella pneumoniae invasive liver abscess syndrome (KPILAS) with endophthalmitis-caused blindness as the first symptom after enema. The patient had diabetes, and his blood glucose was poorly controlled. She developed ...
Mirgul Bayanova,Aigerim Abilova,Alisa Nauryzbayeva et al. Mirgul Bayanova et al.
Perrault syndrome (PRLTS) is a rare autosomal recessive disorder which is associated with pathogenic variants in HSD17B4, HARS2, CLPP, LARS2, GGPS1, RMND1, TWNK, ERAL1, and PRORP genes. The disease is characterized by sensorineural hearing ...
Hunter Montgomery,Matthew X Luo,Steven Baker et al. Hunter Montgomery et al.
Background: Hyperhemolysis syndrome (HS) is a severe hemolytic transfusion reaction that can cause hemoglobin and hematocrit levels to drop below pretransfusion levels, leading to severe anemia. HS most commonly occurs in...
Ilaria Anna Bellofatto,Marta Sessarego,Amedeo Tirandi et al. Ilaria Anna Bellofatto et al.
Introduction: 3-Hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) inhibitors are widely used worldwide to treat dyslipidaemia and prevent cardiovascular events. Statins can cause a wide variety of muscle injuries rang...
Shahla Chaichian,Mohanna Khandan,Samaneh Rokhgireh et al. Shahla Chaichian et al.
This article presents a case of spontaneous autoamputation of ovary in a 46-year-old nulligravid woman with a history of rheumatoid arthritis and hypertension, who presented with secondary amenorrhea and white vaginal discharge. Despite an ...
Alessia Laneri,Stefania Cerri,Giovanni Della Casa et al. Alessia Laneri et al.
Introduction. Acute exacerbation of interstitial lung disease (ILD) and COVID-19 pneumonia show many similarities, but also COVID-19 sequelae, mainly when fibrotic features are present, can be difficult to distinguish from chronic ILD obser...