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Polymer Technology for the Detection and Elimination of Emerging Pollutants
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Clinical Profile and Visual Outcome of Ocular Bartonellosis in Malaysia
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Factors Associated with Placenta Praevia in Primigravidas and Its Pregnancy Outcome
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Magnetically separable silica-chitosan hybrids for efficient phosphate adsorption in aqueous solution
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A review on modified ZnO for the effective degradation of methylene blue and rhodamine B
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Genetic screening strategy for children with hereditary spherocytosis in Jiangxi Province of China
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The type of exercise most beneficial for quality of life in people with atrial fibrillation: a network meta-analysis
Published 2025-01-01“…We conducted comprehensive searches across multiple databases, including PubMed, Web of Science, Embase, Cochrane Library, Scopus, and Chinese databases such as CNKI, WanFang Data, and VIP. The review included only randomized controlled trials (RCTs) that investigated the effects of exercise interventions on HRQoL among individuals diagnosed with AF.ResultsThe network meta-analysis (NMA) incorporated 12 studies, of which five presented some concerns regarding risk of bias and one exhibited a high risk of bias. …”
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A Novel COL7A1 Mutation in a Patient With Dystrophic Epidermolysis Bullosa. Successful Treatment With Upadacitinib
Published 2025-01-01“…Shuqin Lai,* Chunli Lin,* Zimeng Guo, Yun Lai, Ling Xie, Chunlei Wan, Tao Yang, Longnian Li Department of Dermatology, Candidate Branch of National Clinical Research Centre for Skin and Immune Diseases, First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, People’s Republic of China*These authors contributed equally to this workCorrespondence: Tao Yang; Longnian Li, Department of Dermatology, Candidate Branch of National Clinical Research Centre for Skin and Immune Diseases, First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, People’s Republic of China, Email danny20021068@126.com; li_longnian@foxmail.comAbstract: Dystrophic epidermolysis bullosa (DEB) is a heterogeneous and rare genetic skin disease caused by mutations in the COL7A1 gene, which encodes Type VII collagen. …”
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Clinical Efficacy and Meta-Analysis of Stem Cell Therapies for Patients with Brain Ischemia
Published 2016-01-01“…We searched Cochrane Library, PubMed, Ovid, CBM, CNKI, WanFang, and VIP Data from its inception to December 2015, to collect randomized controlled trials (RCT) of stem cell transplantation for the ischemic stroke. …”
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Prevalence and influence factors of hepatic encephalopathy after transjugular intrahepatic portosystemic shunt: a Meta-analysis
Published 2025-01-01“…Objective To systematically evaluate the current status of hepatic encephalopathy (HE) and its influencing factors in patients after transjugular intrahepatic portosystemic shunt (TIPS).Methods Cochrane Library, PubMed, Embase, Web of Science, CINAHL , CNKI, VIP , CBM, WanFang database were searched from inception to October 20, 2024. …”
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