Twin fetuses associated with double amniotic sacs diagnosed using transvaginal ultrasonography: A case report [0.03%]
经阴道超声诊断双胎囊的双羊膜腔单绒毛膜性双胞胎胎儿一例报告
Zheng-Qiao Liang,Wen-Qing Ding
Zheng-Qiao Liang
Background: Conjoined twins are a rare twin malformation commonly presenting as single amniotic sac twinning, with double amniotic sac twinning being extremely rare and poorly reported. Most conjoined twins are females. ...
Muad Abdi Hassan,Abdulqadir J Nashwan
Muad Abdi Hassan
Intensive care unit-acquired weakness (ICU-AW) significantly hampers patient recovery and increases morbidity. With the absence of established preventive strategies, this study utilizes advanced machine learning methodologies to unearth key...
Effect of cetuximab plus FOLFOX4 regimen on clinical outcomes in advanced gastric carcinoma patients receiving evidence-based care [0.03%]
西妥昔单抗联合FOLFOX4方案对接受规范化疗晚期胃癌患者预后影响的研究
Hui Ying,Ren-Jun Huang,Xiao-Min Jing et al.
Hui Ying et al.
Background: Although chemotherapy is effective for treating advanced gastric carcinoma (aGC), it may lead to an adverse prognosis. Establishing a highly effective and low-toxicity chemotherapy regimen is necessary for imp...
Cytokine release syndrome triggered by programmed death 1 blockade (sintilimab) therapy in a psoriasis patient: A case report [0.03%]
程序性死亡配体1抑制剂（信迪利单抗）诱导的细胞因子释放综合征一例报告
Ming-Hui Zhou,Min-Feng Ye,Zhen-Xing Zhang et al.
Ming-Hui Zhou et al.
Background: In recent years, immune checkpoint inhibitors (ICIs) have demonstrated remarkable efficacy across diverse malignancies. Notably, in patients with advanced gastric cancer, the use of programmed death 1 (PD-1) b...
Modified approach of regenerative treatment for distal intrabony defect beneath non-keratinized mucosa at terminal molar: A case report [0.03%]
非角化黏膜下远端牙周骨缺损再生治疗的改良方法——个案报告
Jian-Ru Liu,Yan Huang,Xiang-Ying Ouyang et al.
Jian-Ru Liu et al.
Background: Intrabony defects beneath non-keratinized mucosa are frequently observed at the distal site of terminal molars. Consequently, the application of regenerative treatment using the modified wedge-flap technique i...
Clinical issues and challenges in imaging of gastrointestinal diseases: A minireview and our experience [0.03%]
胃肠病影像检查的临床问题和挑战：小结与体会
Milena Gulinac,Georgi Kiprin,Ivan Tsranchev et al.
Milena Gulinac et al.
Imaging techniques play a crucial role in the modern era of medicine, particularly in gastroenterology. Nowadays, various non-invasive and invasive imaging modalities are being routinely employed to evaluate different gastrointestinal (GI) ...
Facilitating and hindering factors of community nurses' emergency and critical care treatment abilities: A qualitative study [0.03%]
社区护士急诊及重症护理能力的影响因素质性研究
Wen-Lin Cheng,Rui Li,Yan Song et al.
Wen-Lin Cheng et al.
Background: This study adopts a descriptive phenomenological approach to investigate the facilitators and barriers of community nurses' abilities in managing critical and emergency conditions. With the transition of healt...
Vomiting-induced pharyngeal perforation during bowel preparation for colonoscopy: A case report [0.03%]
结肠镜检查肠道准备过程中发生呕吐致咽穿孔1例报告
Geonhee Kim,Won Hyuk Lee,Seokin Kang et al.
Geonhee Kim et al.
Background: Effective bowel cleansing is essential for a successful colonoscopy. Laxatives, such as polyethylene glycol, are commonly used for bowel preparation. Vomiting is a frequent complication during bowel preparatio...
Unveiling significant risk factors for intensive care unit-acquired weakness: Advancing preventive care [0.03%]
重症监护病房获得性衰弱的显著风险因素：推进预防护理
Chun-Yao Cheng,Wen-Rui Hao,Tzu-Hurng Cheng
Chun-Yao Cheng
In this editorial, we discuss an article titled, "Significant risk factors for intensive care unit-acquired weakness: A processing strategy based on repeated machine learning," published in a recent issue of the World Journal of Clinical Ca...
Complex heterozygous mutations in hereditary spherocytosis: A case report [0.03%]
遗传性球形红细胞增多症复杂杂合突变的病例报告
Miao He,Yan-Cheng Lv,Yu-Hong Wei et al.
Miao He et al.
Background: The aim of this study was to investigate the complex heterozygous mutations of ANK1 and SPTA1 in the same individual and improve our understanding of hereditary spherocytosis (HS) in children. We also hope to ...