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期刊名:Journal of clinical and experimental hepatology

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ISSN:0973-6883

e-ISSN:2213-3453

IF/分区:3.4/Q2

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共收录本刊相关文章索引1733
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
Froylan D Martínez-Sánchez,Maria J Corredor-Nassar,Sandra M Feria-Agudelo et al. Froylan D Martínez-Sánchez et al.
Background and objectives: Metabolic dysfunction-associated steatotic liver disease (MASLD) is a major cause of chronic liver disease, primarily due to insulin resistance and type 2 diabetes (T2D). Despite the strong link...
Xiaohui Sui,Junde Zhao,Yuxin Yang et al. Xiaohui Sui et al.
Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) has become one of the major causes of chronic liver disease among adolescents. However, epidemiological studies on MASLD in adolescents are stil...
Amar Mukund,Niraj Kumar,Amol Srivastava et al. Amar Mukund et al.
Since its introduction in 1977, transarterial chemoembolization (TACE) has widely been accepted treatment for unresectable intermediate stage hepatocellular carcinoma (HCC). Conventional TACE (c-TACE) uses an emulsion of chemotherapeutic ag...
Shweta A Singh,Kelika Prakash,Kamal Kajal et al. Shweta A Singh et al.
Cardiovascular disease (CVD) is the leading cause of morbidity and mortality among LT candidates and accounts for up to 40% of the overall mortality within one month. It is influenced by traditional and nontraditional risk factors related t...
Rajesh Rajalingam,Ashwin Rammohan,Ramkiran Cherukuru et al. Rajesh Rajalingam et al.
The introduction of minimally invasive donor hepatectomy (MIDH) operation saw the initiation and incorporation of minimal access surgery into the field of liver transplantation (LT). Several studies, meta-analyses, and consensus guidelines ...
Hani S Aboalam,Marwa K Hassan,Nada El-Domiaty et al. Hani S Aboalam et al.
Wilson disease (WD) is a rare autosomal recessive disorder caused by ATP7B gene mutations, leading to pathological copper accumulation that primarily affects the liver, brain, and eyes. Diagnosing WD remains a significant challenge due to i...
Dipanwita Biswas,Suvradeep Mitra,Ritambhra Nada et al. Dipanwita Biswas et al.
Background and aims: Hepatic infarcts are uncommon vascular lesions due to dual vascular supply of the liver characterized by the peripherally-located wedge-shaped large zones of necrosis in the hepatic parenchyma. They a...