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期刊名:European journal of case reports in internal medicine

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ISSN:2284-2594

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共收录本刊相关文章索引1861
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
Tattvam Shah Tattvam Shah
Introduction: VEXAS (vacuoles, E1-enzyme, X-linked, autoinflammation, and somatic) syndrome is a newly recognized autoinflammatory hematologic condition due to mutations in the UBA1 gene. This case demonstrates its clinic...
Bettina Schreiber,Nicola Hosek,Sebastian Burgener Bettina Schreiber
Introduction: Urinary ascites secondary to spontaneous rupture of the urinary bladder (SRUB) is a rare clinical entity presenting with non-specific symptoms, which poses a significant diagnostic challenge. A specific pres...
João Horta Antunes,Sara Frazão de Brito,Hugo Jorge Alves et al. João Horta Antunes et al.
Tularaemia is a rare zoonosis caused by Francisella tularensis, with only a few reported cases in Western Europe and only 4 notified in Portugal between 2014 and 2021. We describe an imported case diagnosed in Portugal in 2023. A 40-year-ol...
Marta Chiara Sircana,Roberto Manetti,Gavino Casu et al. Marta Chiara Sircana et al.
Introduction: Kounis syndrome is an acute coronary syndrome precipitated by allergic or hypersensitivity reactions and mediated by the release of inflammatory substances that affect the coronary circulation. In spite of i...
Hussein Rabah,Houssein Youness,Awais Bajwa et al. Hussein Rabah et al.
Introduction: A bronchobiliary fistula (BBF) is a rare pathological communication between the biliary tract and the bronchial tree. It is most often associated with hepatic tumours, infections or trauma. The diagnosis can...
Thanh-Huong Truong,Ngoc-Thanh Kim,Doan-Loi Do et al. Thanh-Huong Truong et al.
Background: Adult-onset citrullinemia type II (CTLN2) is a rare autosomal recessive urea cycle disorder caused by mutations in the solute carrier family 25 member 13 (SLC25A13) gene, which encodes citrin-a mitochondrial t...
Coana Sukmagautama,Christopher William Purnomo,Kenneth Tan et al. Coana Sukmagautama et al.
Introduction: Herpes zoster results from reactivation of varicella-zoster virus (VZV) and classically presents with a dermatomal vesicular rash. Disseminated or visceral involvement is uncommon and predominantly occurs in...
Katherine Atallah,Antonio Al Hazzouri,Kaity Saliba et al. Katherine Atallah et al.
Ovarian collision tumours are rare entities defined by the coexistence of two histologically distinct neoplasms, most commonly reported within the same ovary, while bilateral involvement is extremely uncommon and often under-recognised. End...
Nele Carton,Nilüfer Aylin Acet Öztürk,Mine Özşen et al. Nele Carton et al.
Erdheim-Chester disease (ECD) is a rare histiocytic disorder. The underlying etiology has not yet been fully elucidated. Recent technological and molecular advances have identified aberrant activation of the MAPK/ERK signalling pathway as a...