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7篇 您的检索式:作者名="Sonia BA"
    题名 作者 年代 出处 被引量
1Impaired CTLA-4 responses in COPD are associated with systemic inflammation显示文摘Dino BA Tan Sonia Fernandez PatriciaPrice Martyn A French Philip J Thompson Yuben P Moodley 2014Cellular & Molecular Immunology2014,11,6:3
2Randomized Controlled Trial of Aspiration Needle versus Automated Biopsy Device for Transjugular Liver Biopsy显示文摘Rafael Ba?ares Sonia Alonso María-Vega Catalina Marta Casado Diego Rincón Magdalena Salcedo Emilio Alvarez Carmen Guerrero Antonio Echenagusía Fernando Camú?ez Gonzalo Simó 2001Journal of Vascular and Interventional Radiology2001,,5:1
3Over-expression of Dof-type transcription factor increases lipid production in Chlamydomonas reinhardtii显示文摘Alejandro Ibá?ez-Salazar Sergio Rosales-Mendoza Alejandro Rocha-Uribe Jocelín Itzel Ramírez-Alonso Ignacio Lara-Hernández Araceli Hernández-Torres Luz María Teresita Paz-Maldonado Ana Sonia Silva-Ramírez Bernardo Ba?uelos-Hernández José Luis Martínez-Salg 2014Journal of Biotechnology2014,,:1
4Satisfaction and burnout among staff of crisis resolution, assertive outreach and community mental health teams显示文摘Tanya Nelson MBBS MRCPsych MSc Sonia Johnson BA BM BCh MSc MRCPsych DM Prof. Paul Bebbington MA MPhil PhD FRCP FRCPsych 2009Social Psychiatry and Psychiatric Epidemiology2009,,7:1
5CAobal burden of COPD: risk factors, prevalence, and future trends显示文摘Mannirlo DM Sonia BA 2007Lancet2007,370,9589:1
6International variation in the prevalence of COPD (the BOLD Study): a population-based prevalence study显示文摘Sonia BA Mary Ann M Vollmer WM Suzanne G 2007Lancet2007,370,9589:1
7Hepatocellular carcinoma risk after viral response in hepatitis C virus-advanced fibrosis: Who to screen and for how long?显示文摘Hepatitis C virus(HCV)chronic infection is associated with fibrosis progression,end-stage liver complications and HCC.Not surprisingly,HCV infection is a leading cause of liver-related morbidity and mortality worldwide.After sustained virological response(SVR),the risk of developing hepatocellular carcinoma is not completely eliminated in patients with established cirrhosis or with advanced fibrosis.Therefore,lifelong surveillance is currently recommended.This strategy is likely not universally cost-effective and harmless,considering that not all patients with advanced fibrosis have the same risk of developing HCC.Factors related to the severity of liver disease and its potential to improve after SVR,the molecular and epigenetic changes that occur during infection and other associated comorbidities might account for different risk levels and are likely essential for identifying patients who would benefit from screening programs after SVR.Efforts to develop predictive models and risk calculators,biomarkers and genetic panels and even deep learning models to estimate the individual risk of HCC have been made in the direct-acting antiviral agents era,when thousands of patients with advanced fibrosis and cirrhosis have reached SVR.These tools could help to identify patients with very low HCC risk in whom surveillance might not be justified.In this review,factors affecting the probability of HCC development after SVR,the benefits and risks of surveillance,suggested strategies to estimate individualized HCC risk and the current evidence to recommend lifelong surveillance are discussed.Adriana Ahumada Laura Rayón Clara Usón Rafael Bañares Sonia Alonso Lopez 2021World Journal of Gastroenterology2021,27,40:0
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