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期刊名:Therapeutic advances in cardiovascular disease

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ISSN:1753-9447

e-ISSN:1753-9455

IF/分区:2.2/Q2

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共收录本刊相关文章索引417
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
Donovan Cassidy-Nolan,Claudia Cote,Dominique de Waard et al. Donovan Cassidy-Nolan et al.
Pulmonary artery aneurysms (PAAs) are a rare pathology with potentially devastating consequences. In this case series, we describe two cases of clinically isolated pulmonary arteritis and concisely review the literature surrounding this new...
Mohammed AbuBaha,Samia Aldwaik,Ameer Awashra et al. Mohammed AbuBaha et al.
Severe burn injuries result in a massive systemic inflammatory and hypermetabolic response, often disrupting multiple organ systems, including the cardiovascular system. Cardiac troponins are frequently elevated in burn patients, but the in...
Akalu Fetene,Amsalu Degu,Chalelgn Kassaw et al. Akalu Fetene et al.
Background: Guideline-directed medical therapy (GDMT) prolongs survival in patients with heart failure with reduced ejection fraction (HFrEF). However, different countries implement GDMT differently, and many patients are...
Lingwei Huang,Dan Xiao,Meimei Yang et al. Lingwei Huang et al.
Background: Inflammation significantly impacts disease progression and prognosis in acute pulmonary embolism (APE); however, the optimal method to quantify this inflammation for prognostic purposes remains unclear. ...
Marta T/Mariam,Wagari Tuli Nora,Ousman Adal et al. Marta T/Mariam et al.
Background: Rapid interpretation of electrocardiography (ECGs) is essential for reducing patient mortality and morbidity associated with heart conditions. Despite its significance, many healthcare providers struggle to ac...
Maha Sajjad,Rabia Ashraf,Riya Bhagwan et al. Maha Sajjad et al.
Background: Hereditary transthyretin amyloidosis (hATTR) is caused by mutations in the transthyretin (TTR) gene, which lead to the aggregation of misfolded TTR protein and amyloid accumulation in the peripheral nerves, he...
Sherelym Alessandra Maita-Arauco,Sthephanie María Quispe-Vasquez,Vicente Aleixandre Benites-Zapata et al. Sherelym Alessandra Maita-Arauco et al.
Background: Different accessible and low-cost biomarkers have been investigated to stratify patients with acute heart failure (AHF). One of them is the red cell distribution width (RDW), which proved to be a greater progn...
Yohei Takenobu,Noriko Nomura,Yoshito Sugita et al. Yohei Takenobu et al.
Carotid blowout syndrome (CBS) is a potentially fatal condition requiring prompt diagnosis and intervention. CBS primarily affects patients with a history of surgery or irradiation for head and neck malignancies. In this report, we describe...