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"Soon Young Ko"

Original Article

Viral hepatitis

Efficacy and safety of sofosbuvir plus ribavirin for Korean patients with hepatitis C virus genotype 2 infection: A retrospective multi-institutional study
Young Min Kim, Suk Bae Kim, Il Han Song, Sae Hwan Lee, Hong Soo Kim, Tae Hee Lee, Young Woo Kang, Seok Hyun Kim, Byung Seok Lee, Hee Bok Chae, Myeong Jun Song, Ji Woong Jang, Soon Young Ko, Jae Dong Lee
Clin Mol Hepatol 2018;24(3):311-318.
Published online June 4, 2018
DOI: https://doi.org/10.3350/cmh.2017.0070
Background/Aims
Sofosbuvir plus ribavirin is a standard treatment for patients infected with chronic hepatitis C virus (HCV) genotype 2 in Korea. The purpose of this study was to examine the efficacy and safety of this treatment in Korean patients with chronic HCV genotype 2 infection.
Methods
We retrospectively analyzed clinical data of patients treated with sofosbuvir plus ribavirin for chronic HCV genotype 2 from May 2016 to December 2017 at eight hospitals located in the Daejeon-Chungcheong area.
Results
A total of 172 patients were treated with sofosbuvir plus ribavirin. Of them, 163 patients completed the treatment, and 162 patients were tested for sustained virologic response 12 weeks after treatment discontinuation (SVR12). Mean age was 59.6±12.3 years (27–96), and 105 (64.4%) patients were female. Of the total patients, 49 (30.1%) were diagnosed with cirrhosis, and 31 of them were treated for 16 weeks. Sofosbuvir plus ribavirin was the first-line treatment for 144 (88.3%) patients. Eleven (6.7%) patients were intolerant to previous interferon-based treatment. Eight (5.0%) patients relapsed after interferon-based treatment. HCV RNA non-detection rate at 4, 8, and 12 weeks was 97.5%, 99.1%, and 99.3%, respectively, and SVR12 was 98.8% (161/163). During treatment, 18 (11.0%) patients had to reduce their administrated dose of ribavirin because of anemia. One patient stopped the treatment because of severe anemia. Other adverse events, including dizziness, indigestion, and headache, were found in 26 (16.0%) patients.
Conclusions
A 12-16 week treatment with sofosbuvir plus ribavirin is remarkably effective and well tolerated in Korean patients with chronic HCV genotype 2 infection.

Citations

Citations to this article as recorded by  Crossref logo
  • Combination treatment with sofosbuvir and ribavirin for patients diagnosed with hepatitis C genotype 2: A real-world, single-center study
    Ik Sung Choi, Kwang Min Kim, Sang Goon Shim
    Arab Journal of Gastroenterology.2021; 22(1): 23.     CrossRef
  • Real-Life Effectiveness and Safety of Glecaprevir/Pibrentasvir for Korean Patients with Chronic Hepatitis C at a Single Institution
    Young Joo Park, Hyun Young Woo, Jeong Heo, Sang Gyu Park, Young Mi Hong, Ki Tae Yoon, Dong Uk Kim, Gwang Ha Kim, Hyung Hoi Kim, Geun Am Song, Mong Cho
    Gut and Liver.2021; 15(3): 440.     CrossRef
  • Sofosbuvir‐based therapies in genotype 2 hepatitis C virus cirrhosis: A real‐life experience with focus on ribavirin dose
    Carlo Smirne, Antonio D'Avolio, Mattia Bellan, Alessandro Gualerzi, Maria G. Crobu, Mario Pirisi
    Pharmacology Research & Perspectives.2021;[Epub]     CrossRef
  • Novel variant in glycophorin c gene protects against ribavirin-induced anemia during chronic hepatitis C treatment
    Jennifer J. Lin, Catrina M. Loucks, Jessica N. Trueman, Britt I. Drögemöller, Galen E.B. Wright, Eric M. Yoshida, Jo-Ann Ford, Samuel S. Lee, Richard B. Kim, Bandar Al-Judaibi, Ute I. Schwarz, Alnoor Ramji, Edward Tam, Colin J. Ross, Bruce C. Carleton
    Biomedicine & Pharmacotherapy.2021; 143: 112195.     CrossRef
  • Incidence, risk factors and impact on virological response of anemia in chronic genotype 2 hepatitis C receiving sofosbuvir plus ribavirin
    Chi-Ching Chen, Shui-Yi Tung, Kuo-Liang Wei, Chien-Heng Shen, Te-Sheng Chang, Wei-Ming Chen, Huang-Wei Xu, Chih-Wei Yen, Yi-Hsing Chen, Sheng-Nan Lu, Chao-Hung Hung
    Journal of the Formosan Medical Association.2020; 119(1): 532.     CrossRef
  • Hepatocellular Carcinoma Risk According to Regimens for Eradication of Hepatitis C Virus; Interferon or Direct Acting Antivirals
    Hye Won Lee, Dai Hoon Han, Hye Jung Shin, Jae Seung Lee, Seung Up Kim, Jun Yong Park, Do Young Kim, Sang Hoon Ahn, Beom Kyung Kim
    Cancers.2020; 12(11): 3414.     CrossRef
  • Real-Life Effectiveness and Safety of Sofosbuvir-Based Therapy in Genotype 2 Chronic Hepatitis C Patients in South Korea, with Emphasis on the Ribavirin Dose
    Eun Sun Jang, Kyung-Ah Kim, Young Seok Kim, In Hee Kim, Byung Seok Lee, Youn Jae Lee, Woo Jin Chung, Sook-Hyang Jeong
    Gut and Liver.2020; 14(6): 775.     CrossRef
  • Direct-acting antivirals in East Asian hepatitis C patients: real-world experience from the REAL-C Consortium
    Chung-Feng Huang, Etsuko Iio, Dae Won Jun, Eiichi Ogawa, Hidenori Toyoda, Yao-Chun Hsu, Hiroaki Haga, Shinji Iwane, Masaru Enomoto, Dong Hyun Lee, Grace Wong, Chen-Hua Liu, Toshifumi Tada, Wan-Long Chuang, Ramsey Cheung, Jun Hayashi, Cheng-Hao Tseng, Sato
    Hepatology International.2019; 13(5): 587.     CrossRef
  • Comparison of the Clinical Characteristics and Outcomes between Leprosy-Affected Persons in Sorokdo and the General Population Affected by Chronic Hepatitis C in Korea
    Young-Hwan Ahn, Hyungcheol Park, Myeon Jae Lee, Dong Hyun Kim, Sung Bum Cho, Eunae Cho, Chung Hwan Jun, Sung Kyu Choi
    Gut and Liver.2019; 13(5): 549.     CrossRef
  • Does the old-fashioned sofosbuvir plus ribavirin treatment in genotype 2 chronic hepatitis C patients still works for Koreans?
    Jong Eun Yeon
    Clinical and Molecular Hepatology.2018; 24(3): 294.     CrossRef
  • Ribavirin/sofosbuvir

    Reactions Weekly.2018; 1727(1): 247.     CrossRef
  • 11,165 View
  • 206 Download
  • 11 Web of Science
  • Crossref

Review

Viral hepatitis

The advent of novel, direct-acting antiviral (DAA) regimens for hepatitis C viral (HCV) infection has revolutionized its treatment by producing a sustained virologic response of more than 95% with few side effects and no comorbidities in the general population. Until recently, ideal DAA regimens have not been available to patients with severe renal impairment and end-stage renal disease because there are limited data on the pharmacokinetics, safety, and efficacy of treatment in this unique population. In a hemodialysis context, identifying patients in need of treatment and preventing HCV transmission may also be a matter of concern. Recently published studies suggest that a combination of paritaprevir/ ritonavir/ombitasvir and dasabuvir, elbasvir/grazoprevir, or glecaprevir/pibrentasir successfully treats HCV infection in chronic kidney disease stage 4 or 5 patients with or without hemodialysis.

Citations

Citations to this article as recorded by  Crossref logo
  • The remaining challenges of HCV treatment in the direct‐acting antivirals era
    Beom Kyung Kim, Sang Hoon Ahn
    Journal of Gastroenterology and Hepatology.2019; 34(11): 1891.     CrossRef
  • 13,521 View
  • 356 Download
  • 4 Web of Science
  • Crossref

Original Articles

Viral hepatitis

Clinical impact of the early alanine amininotransferase flare during tenofovir monotherapy in treatment-naïve patients with chronic hepatitis B
Hee Yeon Seo, Han Ah Lee, Soon Young Ko, Joon Ho Wang, Jeong Han Kim, Won Hyeok Choe, So Young Kwon
Clin Mol Hepatol 2017;23(2):154-159.
Published online May 8, 2017
DOI: https://doi.org/10.3350/cmh.2016.0067
Background/Aims
Little is known about the effect of early flares on response during first-line tenofovir disoproxil fumarate (TDF) treatment for chronic hepatitis B (CHB). The aim of this study was to investigate the incidence and outcome of early alanine aminotransferase (ALT) flare in treatment-naive patients with CHB during long-term TDF monotherapy. Methods: One hundred eighty-one treatment-naive CHB patients were treated with a 300-mg once-daily dose of TDF for more than 12 weeks. Virological markers of hepatitis B virus (HBV) and biochemical data were measured at baseline and every 4-12 weeks during the therapy. The proportion of patients with undetectable HBV DNA level (< 100 copies/mL) was noted. Results: The median age was 48.3 years and 122 patients (67.4%) were men. Hepatitis B envelope antigen (HBeAg) was positive in 101 patients (55.8%). No patient had cirrhosis. The median follow-up duration was 45 weeks (12-155 weeks). ALT flare (>5 × upper limit of the normal range) occurred in seven patients (3%) without viral breakthrough within the first 8 weeks after the start of TDF monotherapy. Among them, six patients were HBeAg-positive and one patient was HBeAg-negative. All cases of early ALT flares resolved within 4 weeks and virologic response was observed in all patients without interruption or discontinuation of treatment. Conclusions: Continuous TDF monotherapy was effective and safe in treatment-naive patients with CHB who experienced early ALT flares followed by a decrease in HBV DNA level.

Citations

Citations to this article as recorded by  Crossref logo
  • Efficacy, safety, and pharmacokinetics of capsid assembly modulator linvencorvir plus standard of care in chronic hepatitis B patients
    Jinlin Hou, Edward Gane, Rozalina Balabanska, Wenhong Zhang, Jiming Zhang, Tien Huey Lim, Qing Xie, Chau-Ting Yeh, Sheng-Shun Yang, Xieer Liang, Piyawat Komolmit, Apinya Leerapun, Zenghui Xue, Ethan Chen, Yuchen Zhang, Qiaoqiao Xie, Ting-Tsung Chang, Tsun
    Clinical and Molecular Hepatology.2024; 30(2): 191.     CrossRef
  • DFT, molecular docking and ADME prediction of tenofovir drug as a promising therapeutic inhibitor of SARS-CoV-2 Mpro
    Siyamak Shahab, Masoome Sheikhi, Maksim Khancheuski, Hooriye Yahyaei, Hora Alhosseini Almodarresiyeh, Sadegh Kaviani
    Main Group Chemistry.2023; 22(1): 115.     CrossRef
  • Switching from Tenofovir-Based Combination Therapy to Tenofovir Monotherapy in Multidrug-Experienced Chronic Hepatitis B Patients: a 5-Year Experience at Two Centers
    Jung Hun Kim, Jeong Han Kim, Won Hyeok Choe, So Young Kwon, Byung-chul Yoo, Eileen L. Yoon, Seong Hee Kang
    Antimicrobial Agents and Chemotherapy.2022;[Epub]     CrossRef
  • Benefit of transaminase elevations in establishing functional cure of HBV infection during nap‐based combination therapy
    Michel Bazinet, Victor Pântea, Gheorghe Placinta, Iurie Moscalu, Valentin Cebotarescu, Lilia Cojuhari, Pavlina Jimbei, Liviu Iarovoi, Valentina Smesnoi, Tatiana Musteata, Alina Jucov, Ulf Dittmer, Adalbert Krawczyk, Andrew Vaillant
    Journal of Viral Hepatitis.2021; 28(5): 817.     CrossRef
  • Transaminase Elevations during Treatment of Chronic Hepatitis B Infection: Safety Considerations and Role in Achieving Functional Cure
    Andrew Vaillant
    Viruses.2021; 13(5): 745.     CrossRef
  • Safety, pharmacokinetics, and antiviral activity of RO7049389, a core protein allosteric modulator, in patients with chronic hepatitis B virus infection: a multicentre, randomised, placebo-controlled, phase 1 trial
    Man-Fung Yuen, Xue Zhou, Edward Gane, Christian Schwabe, Tawesak Tanwandee, Sheng Feng, Yuyan Jin, Miriam Triyatni, Annabelle Lemenuel-Diot, Valerie Cosson, Zenghui Xue, Remi Kazma, Qingyan Bo
    The Lancet Gastroenterology & Hepatology.2021; 6(9): 723.     CrossRef
  • Tenofovir disoproxil fumarate-induced severe liver injury in a patient with chronic hepatitis B virus infection
    Min Kyu Kang, Jung Gil Park
    Digestive and Liver Disease.2018; 50(6): 628.     CrossRef
  • Is alanine aminotransferase flare-up in nucleos(t)ide analogue treatment of chronic hepatitis B a promising, rather than a devastating, sign?
    Nae-Yun Heo
    Clinical and Molecular Hepatology.2017; 23(2): 125.     CrossRef
  • 10,356 View
  • 184 Download
  • 8 Web of Science
  • Crossref

Viral hepatitis

The efficacy of tenofovir-based therapy in patients showing suboptimal response to entecavir-adefovir combination therapy
Jeong Han Kim, Sung Hyun Ahn, Soon Young Ko, Won Hyeok Choe, Kyun-Hwan Kim, So Young Kwon
Clin Mol Hepatol 2016;22(2):241-249.
Published online June 15, 2016
DOI: https://doi.org/10.3350/cmh.2015.0053
Background/Aims
Before tenofovir (TDF) become available in South Korea, combination therapy with entecavir (ETV) and adefovir (ADV) was the most potent regimen for chronic hepatitis B (CHB) patients who fail to respond to rescue therapy for drug resistance. We analyzed the efficacy of ETV-ADV combination therapy and investigated the clinical and clonal results of TDF-based rescue therapy in CHB patients refractory to this combination. Methods: We retrospectively reviewed the medical records of CHB patients treated for up to 3 years with ETV-ADV combination therapy as a rescue therapy for drug resistance. In cases refractory to this combination, clinical and clonal analyses were performed for TDF-based rescue therapy. Results: The analysis was performed on 48 patients. Twelve patients achieved a virological response (VR) within 3 years. A VR was subsequently achieved in nine of the ten patients without a VR who switched to TDF monotherapy. A VR was also achieved in six of the seven patients who switched to lamivudine-TDF combination therapy, and in two of the two patients who switched to ETV-TDF combination therapy. In an in vitro susceptibility test, viral replication was detected with TDF monotherapy but not with ETV-TDF combination therapy. Conclusions: The efficacy of ETV-ADV combination therapy was insufficient in CHB patients who were refractory to rescue therapy. A more potent regimen such as ETV-TDF combination therapy may be considered in such refractory cases.

Citations

Citations to this article as recorded by  Crossref logo
  • Switching from Tenofovir-Based Combination Therapy to Tenofovir Monotherapy in Multidrug-Experienced Chronic Hepatitis B Patients: a 5-Year Experience at Two Centers
    Jung Hun Kim, Jeong Han Kim, Won Hyeok Choe, So Young Kwon, Byung-chul Yoo, Eileen L. Yoon, Seong Hee Kang
    Antimicrobial Agents and Chemotherapy.2022;[Epub]     CrossRef
  • Delayed viral suppression during antiviral therapy is associated with increased hepatocellular carcinoma rates in HBeAg‐positive high viral load chronic hepatitis B
    J. Y. Nam, Y. Chang, H. Cho, S. H. Kang, Y. Y. Cho, E. J. Cho, J.‐H. Lee, S. J. Yu, J.‐H. Yoon, Y. J. Kim
    Journal of Viral Hepatitis.2018; 25(5): 552.     CrossRef
  • Adherence, virological outcome, and drug resistance in Chinese HIV patients receiving first-line antiretroviral therapy from 2011 to 2015
    Pengtao Liu, Lingjie Liao, Wei Xu, Jing Yan, Zhongbao Zuo, Xuebing Leng, Jing Wang, Wei Kan, Yinghui You, Hui Xing, Yuhua Ruan, Yiming Shao
    Medicine.2018; 97(50): e13555.     CrossRef
  • Is the tenofovir based therapy almighty for previous treatment failure in chronic hepatitis B?
    Hyung Joon Yim
    Clinical and Molecular Hepatology.2016; 22(2): 238.     CrossRef
  • 12,859 View
  • 141 Download
  • 4 Web of Science
  • Crossref

Case Report

Viral hepatitis

Reversible splenial lesion on the corpus callosum in nonfulminant hepatitis A presenting as encephalopathy
Soon Young Ko, Byung Kook Kim, Dong Wook Kim, Jeong Han Kim, Won Hyeok Choe, Hee Yeon Seo, So Young Kwon
Clin Mol Hepatol 2014;20(4):398-401.
Published online December 24, 2014
DOI: https://doi.org/10.3350/cmh.2014.20.4.398

Reversible focal lesions on the splenium of the corpus callosum (SCC) have been reported in patients with mild encephalitis/encephalopathy caused by various infectious agents, such as influenza, mumps, adenovirus, Varicella zoster, Escherichia coli, Legionella pneumophila, and Staphylococcus aureus. We report a case of a reversible SCC lesion causing reversible encephalopathy in nonfulminant hepatitis A. A 30-year-old healthy male with dysarthria and fever was admitted to our hospital. After admission his mental status became confused, and so we performed electroencephalography (EEG) and magnetic resonance imaging (MRI) of the brain, which revealed an intensified signal on diffusion-weighted imaging (DWI) at the SCC. His mental status improved 5 days after admission, and the SCC lesion had completely disappeared 15 days after admission.

Citations

Citations to this article as recorded by  Crossref logo
  • A rare cause of dysarthria: Legionnaires’ disease
    Emine Afsin, Furkan Küçük, Serpil Yıldız, Sadettin Ersoy
    International Journal of Neuroscience.2025; 135(2): 168.     CrossRef
  • Clinical Characteristics of H1N1 Influenza A-Associated Mild Encephalopathy with Reversible Splenial Lesion: 4 Pediatric Cases
    Xu-fang Li, Bin Ai, Jia-wei Ye, Li-mei Tan, Hua-mei Yang, Chun-xiao Fang, Lan-hui She, Yi Xu
    Current Medical Science.2021; 41(4): 815.     CrossRef
  • Corpus Callosum Involvement as Extrahepatic Manifestation of Hepatitis E Virus: An Uncommon Entity
    Monika Singla, Parth Bansal, Venkatesh Sajja, Kapil Dev
    Journal of Neurosciences in Rural Practice.2021; 12: 427.     CrossRef
  • Reversible Splenial Lesion Syndrome with Some Novel Causes and Clinical Manifestations
    Pei-lin Lu, John F. Hodes, Xu Zheng, Xing-yue Hu
    Internal Medicine.2020; 59(20): 2471.     CrossRef
  • Electroencephalogram Abnormalities in Very Young Children with Acute Hepatitis A Infection: A Cross-Sectional Study
    Iraj Shahramian, Mohammad Hassan Mohammadi, Alireza Akbari, Alireza Sargazi, Mojtaba Delaramnasab, Ali Bazi
    Journal of Comprehensive Pediatrics.2019;[Epub]     CrossRef
  • Legionnaires Disease With Focal Neurologic Deficits and a Reversible Lesion in the Splenium of the Corpus Callosum
    Jillian E. Raybould, Megan E. Conroy, Joseph G. Timpone, Princy N. Kumar
    Infectious Diseases in Clinical Practice.2017; 25(1): 13.     CrossRef
  • MR imaging of adult acute infectious encephalitis
    A. Bertrand, D. Leclercq, L. Martinez-Almoyna, N. Girard, J.-P. Stahl, T. De-Broucker
    Médecine et Maladies Infectieuses.2017; 47(3): 195.     CrossRef
  • Mild encephalitis/encephalopathy with reversible splenial lesion (MERS) in adults-a case report and literature review
    Junliang Yuan, Shuna Yang, Shuangkun Wang, Wei Qin, Lei Yang, Wenli Hu
    BMC Neurology.2017;[Epub]     CrossRef
  • Clinically mild encephalitis/encephalopathy with a reversible splenial lesion caused by methicillin-sensitive Staphylococcus aureus bacteremia with toxic shock syndrome: a case report
    Koki Kosami, Tsuneaki Kenzaka, Yuka Sagara, Kensuke Minami, Masami Matsumura
    BMC Infectious Diseases.2016;[Epub]     CrossRef
  • Reversible splenial lesion syndrome associated with lobar pneumonia
    Chunrong Li, Xiujuan Wu, Hehe Qi, Yanwei Cheng, Bing Zhang, Hongwei Zhou, Xiaohong Lv, Kangding Liu, Hong-Liang Zhang
    Medicine.2016; 95(39): e4798.     CrossRef
  • 10,248 View
  • 120 Download
  • 11 Web of Science
  • Crossref
Original Articles

Viral hepatitis

Hepatitis B surface antigen levels at 6 months after treatment can predict the efficacy of lamivudine-adefovir combination therapy in patients with lamivudine-resistant chronic hepatitis B
Jeong Han Kim, Hee Won Moon, Soon Young Ko, Won Hyeok Choe, So Young Kwon
Clin Mol Hepatol 2014;20(3):274-282.
Published online September 25, 2014
DOI: https://doi.org/10.3350/cmh.2014.20.3.274
Background/Aims

Quantitation of hepatitis B surface antigen (HBsAg) is an increasingly popular method to determine the treatment response in chronic hepatitis B (CHB) patients. The clinical value of HBsAg level measurement during rescue therapy for lamivudine (LMV)-resistant CHB patients have not been evaluated to date. Therefore, this study investigated the correlation between HBsAg level and treatment response in LMV-resistant CHB patients treated with adefovir (ADV) add-on therapy.

Methods

LMV-resistant CHB patients treated with LMV-ADV combination therapy for over 2 years were included. HBsAg levels were measured at 6 month intervals until 1 year, and annually thereafter. Treatment response was assessed by determining the virological response (VR, undetectable HBV DNA levels) during treatment.

Results

Fifty patients were included, of which 40 showed a VR. HBsAg levels were not different significantly at baseline (4.0 vs. 3.6 Log10 IU/mL, P=0.072). However, the HBsAg level decreased after 6 months of treatment in patients with a VR and became different significantly between the groups thereafter (3.9 vs. 3.3 at 6 months, P=0.002; 3.8 vs. 3.2 at 1 year, P=0.004; 3.9 vs. 3.2 at 2 years, P=0.008; 3.7 vs. 3.1 at 3 years, P =0.020).

Conclusions

The HBsAg level at 6 months after treatment can help predict treatment response.

Citations

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  • Blood Levels of Glutamine and Nitrotyrosine in Patients with Chronic Viral Hepatitis
    Hussam Murad, Haythum O Tayeb, Mahmoud Mosli, Misbahuddin Rafeeq, Mohammed Basheikh
    International Journal of General Medicine.2021; Volume 14: 8753.     CrossRef
  • The efficacy of tenofovir-based therapy in patients showing suboptimal response to entecavir-adefovir combination therapy
    Jeong Han Kim, Sung Hyun Ahn, Soon Young Ko, Won Hyeok Choe, Kyun-Hwan Kim, So Young Kwon
    Clinical and Molecular Hepatology.2016; 22(2): 241.     CrossRef
  • 9,562 View
  • 48 Download
  • 3 Web of Science
  • Crossref

Liver fibrosis, cirrhosis, and portal hypertension

Prevalence of renal dysfunction in patients with cirrhosis according to ADQI-IAC working party proposal
Yun Jung Choi, Jeong Han Kim, Ja Kyung Koo, Cho I Lee, Ji Young Lee, Jae Hoon Yang, Soon Young Ko, Won Hyeok Choe, So Young Kwon, Chang Hong Lee
Clin Mol Hepatol 2014;20(2):185-191.
Published online June 30, 2014
DOI: https://doi.org/10.3350/cmh.2014.20.2.185
Background/Aims

A revised classification system for renal dysfunction in patients with cirrhosis was proposed by the Acute Dialysis Quality Initiative and the International Ascites Club Working Group in 2011. The aim of this study was to determine the prevalence of renal dysfunction according to the criteria in this proposal.

Methods

The medical records of cirrhotic patients who were admitted to Konkuk University Hospital between 2006 and 2010 were reviewed retrospectively. The data obtained at first admission were collected. Acute kidney injury (AKI) and chronic kidney disease (CKD) were defined using the proposed diagnostic criteria of kidney dysfunction in cirrhosis.

Results

Six hundred and forty-three patients were admitted, of whom 190 (29.5%), 273 (42.5%), and 180 (28.0%) were Child-Pugh class A, B, and C, respectively. Eighty-three patients (12.9%) were diagnosed with AKI, the most common cause for which was dehydration (30 patients). Three patients had hepatorenal syndrome type 1 and 26 patients had prerenal-type AKI caused by volume deficiency after variceal bleeding. In addition, 22 patients (3.4%) were diagnosed with CKD, 1 patient with hepatorenal syndrome type 2, and 3 patients (0.5%) with AKI on CKD.

Conclusions

Both AKI and CKD are common among hospitalized cirrhotic patients, and often occur simultaneously (16.8%). The most common type of renal dysfunction was AKI (12.9%). Diagnosis of type 2 hepatorenal syndrome remains difficult. A prospective cohort study is warranted to evaluate the clinical course in cirrhotic patients with renal dysfunction.

Citations

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  • Mortality of Acute Kidney Injury in Cirrhosis: A Systematic Review and Meta‐Analysis of Over 5 Million Patients Across Different Clinical Settings
    Vasileios Lekakis, Florence Wong, Aikaterini Gkoufa, George V. Papatheodoridis, Evangelos Cholongitas
    Alimentary Pharmacology & Therapeutics.2025; 61(3): 420.     CrossRef
  • A novel risk-predicted nomogram for acute kidney injury progression in decompensated cirrhosis: a double-center study in Vietnam
    Nghia N. Nguyen, Bao T. Nguyen, Thuy D. T. Nguyen, Tam T. T. Tran, Tan N. H. Mai, Huyen N. T. Le, Hoang N. Dang, Vy B. N. Nguyen, Nhi Y. T. Ngo, Cuong T. Vo
    International Urology and Nephrology.2025; 57(7): 2279.     CrossRef
  • Gynura procumbens leaf extract-loaded self-microemulsifying drug delivery system offers enhanced protective effects in the hepatorenal organs of the experimental rats
    Manik Chandra Shill, Md. Faisal Bin Jalal, Madhabi Lata Shuma, Patricia Prova Mollick, Md. Abdul Muhit, Shimul Halder, Miquel Vall-llosera Camps
    PLOS ONE.2025; 20(2): e0304435.     CrossRef
  • Biopharmaceutical characterization of Ajwain (Carum copticum) seed extract-loaded self-microemulsifying drug delivery system for enhanced hepatoprotective and nephroprotective activity
    Shimul Halder, Fatema-Tuz-Zohora, Tania Ahmed Chowdhury, Leon Bhowmik, Madhabi Lata Shuma, Harinarayan Das, Sulobh Sarkar, Md. Abdul Muhit, Manik Chandra Shill
    Scientific Reports.2025;[Epub]     CrossRef
  • Fibrotic Burden in Patients With Hepatitis B Virus–Related Cirrhosis Is Independently Associated With Poorer Kidney Outcomes
    Chan-Young Jung, Hui-Yun Jung, Hyung Woo Kim, Geun Woo Ryu, Jung Il Lee, Sang Hoon Ahn, Seung Up Kim, Beom Seok Kim
    The Journal of Infectious Diseases.2024; 229(1): 108.     CrossRef
  • Study of prevalence, risk factors for acute kidney injury, and mortality in liver cirrhosis patients
    Pooja Basthi Mohan, Shankar Prasad Nagaraju, Balaji Musunuri, Siddheesh Rajpurohit, Ganesh Bhat, Shiran Shetty
    Irish Journal of Medical Science (1971 -).2024; 193(4): 1817.     CrossRef
  • Incidence and risk factors of acute kidney injury in cirrhosis: a systematic review and meta-analysis of 5,202,232 outpatients, inpatients, and ICU-admitted patients
    Vasileios Lekakis, Aikaterini Gkoufa, John Vlachogiannakos, George V. Papatheodoridis, Evangelos Cholongitas
    Expert Review of Gastroenterology & Hepatology.2024; 18(7): 377.     CrossRef
  • Acute kidney injury development and impact on clinical and economic outcomes in patients with cirrhosis: an observational cohort study over a 10-year period
    Osama Y. Alshogran, Shoroq M. Altawalbeh, Eman M. Almestarihi
    European Journal of Gastroenterology & Hepatology.2023; 35(4): 497.     CrossRef
  • Addition of Kidney Dysfunction Type to MELD-Na for the Prediction of Survival in Cirrhotic Patients Awaiting Liver Transplantation in Comparison with MELD 3.0 with Albumin
    Kyeong-Min Yeom, Jong-In Chang, Jeong-Ju Yoo, Ji Eun Moon, Dong Hyun Sinn, Young Seok Kim, Sang Gyune Kim
    Diagnostics.2023; 14(1): 39.     CrossRef
  • Acute Kidney Injury in Patients with Liver Cirrhosis: Prevalence, Predictors, and In‐Hospital Mortality at a District Hospital in Ghana
    Amoako Duah, Francisca Duah, Daniel Ampofo-Boobi, Bright Peprah Addo, Foster Osei-Poku, Adwoa Agyei-Nkansah, Maria Irene Bellini
    BioMed Research International.2022;[Epub]     CrossRef
  • Impact of acute kidney injury on the risk of mortality in patients with cirrhosis: a systematic review and meta-analysis
    Yunfeng Ning, Xiaoyue Zou, Jing Xu, Xiao Wang, Min Ding, Hulin Lu
    Renal Failure.2022; 44(1): 1934.     CrossRef
  • Keeping Patients with End-Stage Liver Disease Alive While Awaiting Transplant
    Andres F. Carrion, Paul Martin
    Clinics in Liver Disease.2021; 25(1): 103.     CrossRef
  • Chronic renal dysfunction in cirrhosis: A new frontier in hepatology
    Ramesh Kumar, Rajeev Nayan Priyadarshi, Utpal Anand
    World Journal of Gastroenterology.2021; 27(11): 990.     CrossRef
  • Predictors of Development of Hepatorenal Syndrome in Hospitalized Cirrhotic Patients with Acute Kidney Injury
    Roula Sasso, Ahmad Abou Yassine, Liliane Deeb
    Journal of Clinical Medicine.2021; 10(23): 5621.     CrossRef
  • Urinary neutrophil gelatinase-associated lipocalin: Acute kidney injury in liver cirrhosis
    Pooja Basthi Mohan, Shankar Prasad Nagaraju, Dharshan Rangaswamy, Balaji Musunuri, Ravindra Prabhu Attur, Ganesh Bhat, Shailesh, Shiran Shetty
    Clinica Chimica Acta.2021; 523: 339.     CrossRef
  • Acute kidney injury and hepatorenal syndrome in cirrhosis
    Kapil Gupta, Abhishek Bhurwal, Cindy Law, Scott Ventre, Carlos D Minacapelli, Savan Kabaria, You Li, Christopher Tait, Carolyn Catalano, Vinod K Rustgi
    World Journal of Gastroenterology.2021; 27(26): 3984.     CrossRef
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    Andres F. Carrion, Ramya Radhakrishnan, Paul Martin
    Expert Review of Gastroenterology & Hepatology.2020; 14(1): 1.     CrossRef
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    Clinical Imaging.2020; 62: 63.     CrossRef
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    Erik L. Lum, Piyavadee Homkrailas, Suphamai Bunnapradist
    Journal of Clinical Gastroenterology.2020; 54(4): 314.     CrossRef
  • Incidence, Mortality and Predictors of Acute Kidney Injury in Patients with Cirrhosis: A Systematic Review and Meta-analysis
    Raseen Tariq, Yousaf Hadi, Khusdeep Chahal, Sivani Reddy, Habeeb Salameh, Ashwani K. Singal
    Journal of Clinical and Translational Hepatology.2020; 8(2): 135.     CrossRef
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    Paulo Henrique Lima, Boyan Fan, Joshua Bérubé, Milena Cerny, Damien Olivié, Jeanne-Marie Giard, Catherine Beauchemin, An Tang
    American Journal of Roentgenology.2019; 213(1): 17.     CrossRef
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    Florence Wong, K. Rajender Reddy, Jacqueline G. O’Leary, Puneeta Tandon, Scott W. Biggins, Guadalupe Garcia‐Tsao, Benedict J. Maliakkal, Jennifer C. Lai, Michael B. Fallon, Hugo E. Vargas, Ram Subramanian, Paul J. Thuluvath, Patrick S. Kamath, Leroy Thack
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    Hamza Waqar Bhatti, Umama Tahir, Noman Ahmed Chaudhary, Sania Bhatti, Muhammad Hafeez, Zuhair Ali Rizvi
    BMJ Open Gastroenterology.2019; 6(1): e000286.     CrossRef
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    Apurva S. Shah, Deepak N. Amarapurkar
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  • Renal dysfunction in liver cirrhosis and its correlation with Child-Pugh score and MELD score
    G A Siregar, M Gurning
    IOP Conference Series: Earth and Environmental Science.2018; 125: 012214.     CrossRef
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    Clinical and Molecular Hepatology.2018; 24(3): 230.     CrossRef
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    Cheng-Yi Chen, Cheng-Jui Lin, Chih-Sheng Lin, Fang-Ju Sun, Chi-Feng Pan, Han-Hsiang Chen, Chih-Jen Wu
    Oncotarget.2018; 9(2): 2236.     CrossRef
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    Andrew Davenport, Mohammed Faisal Sheikh, Edmund Lamb, Banwari Agarwal, Rajiv Jalan
    Kidney International.2017; 92(5): 1058.     CrossRef
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    Su Mi Lee, Young Ki Son, Seong Eun Kim, Won Suk An
    Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis.2017; 37(3): 314.     CrossRef
  • Appréciation du débit de filtration glomérulaire et de la dysfonction rénale chez le cirrhotique
    C. Mousseaux, A. Bouguerba, S. Ayed, J. Barchasz, M. Boukari, D. Goldgran-Toledano, C. Bornstain, F. Vincent
    Réanimation.2016; 25(S3): 137.     CrossRef
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    H. K. Aggarwal, Deepak Jain, Suhas Singla, Promil Jain
    Renal Failure.2015; 37(9): 1457.     CrossRef
  • 13,218 View
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Liver fibrosis, cirrhosis, and portal hypertension

The refit model for end-stage liver disease-Na is not a better predictor of mortality than the refit model for end-stage liver disease in patients with cirrhosis and ascites
Jun Jae Kim, Jeong Han Kim, Ja Kyung Koo, Yun Jung Choi, Soon Young Ko, Won Hyeok Choe, So Young Kwon
Clin Mol Hepatol 2014;20(1):47-55.
Published online March 26, 2014
DOI: https://doi.org/10.3350/cmh.2014.20.1.47
Background/Aims

The modification of the Model for End-Stage Liver Disease (MELD) scoring system (Refit MELD) and the modification of MELD-Na (Refit MELDNa), which optimized the MELD coefficients, were published in 2011. We aimed to validate the superiority of the Refit MELDNa over the Refit MELD for the prediction of 3-month mortality in Korean patients with cirrhosis and ascites.

Methods

We reviewed the medical records of patients admitted with hepatic cirrhosis and ascites to the Konkuk University Hospital between January 2006 and December 2011. The Refit MELD and Refit MELDNa were compared using the predictive value of the 3-month mortality, as assessed by the Child-Pugh score.

Results

In total, 530 patients were enrolled, 87 of whom died within 3 months. Alcohol was the most common etiology of their cirrhosis (n=271, 51.1%), and the most common cause of death was variceal bleeding (n=20, 23%). The areas under the receiver operating curve (AUROCs) for the Child-Pugh, Refit MELD, and Refit MELDNa scores were 0.754, 0.791, and 0.764 respectively; the corresponding values when the analysis was performed only in patients with persistent ascites (n=115) were 0.725, 0.804, and 0.796, respectively. The significant difference found among the Child-Pugh, Refit MELD, and Refit MELDNa scores was between the Child-Pugh score and Refit MELD in patients with persistent ascites (P=0.039).

Conclusions

Refit MELD and Refit MELDNa exhibited good predictability for 3-month mortality in patients with cirrhosis and ascites. However, Refit MELDNa was not found to be a better predictor than Refit MELD, despite the known relationship between hyponatremia and mortality in cirrhotic patients with ascites.

Citations

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  • Multimodal ultrasound: a non-invasive method for identifying dedifferentiation of papillary thyroid carcinoma during active surveillance
    Qian-Yi Dou, Huan-Ling Guo, Wan-Bing Qiu, Ming Xu, Shu-Ling Chen, Xiao-Er Zhang, Xiao-Yan Xie, Jin-Yu Liang
    Frontiers in Oncology.2025;[Epub]     CrossRef
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    Alexandros Hadjivasilis, Alexander Tzanis, Kalliopi J. Ioakim, Ioanna Poupoutsi, Aris P. Agouridis, Panayiotis Kouis
    European Journal of Gastroenterology & Hepatology.2021; 33(3): 312.     CrossRef
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    Peijie Wang, Gang Huang, Ngalei Tam, Chenglin Wu, Shunjun Fu, Bridget P. Hughes, Linwei Wu, Xiaoshun He
    European Journal of Gastroenterology & Hepatology.2016; 28(10): 1210.     CrossRef
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  • 6 Web of Science
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Viral hepatitis

HBsAg level and clinical course in patients with chronic hepatitis B treated with nucleoside analogue: five years of follow-up data
Jeong Han Kim, Yun Jung Choi, Hee Won Moon, Soon Young Ko, Won Hyeok Choe, So Young Kwon
Clin Mol Hepatol 2013;19(4):409-416.
Published online December 28, 2013
DOI: https://doi.org/10.3350/cmh.2013.19.4.409
Background/Aims

Quantification of the hepatitis B surface antigen (HBsAg) is increasingly used to determine the treatment response in patients with chronic hepatitis B (CHB). However, there are limited data about the clinical implications of Quantification of HBsAg long-term nucleoside analogue treatment for CHB. We investigated the clinical correlation between HBsAg level and clinical course in patients with CHB who are treated long-term with nucleoside analogues.

Methods

Patients with CHB who started lamivudine or entecavir monotherapy before June 2007 were enrolled. HBsAg was quantified at baseline, at 6 months, and at 1, 2, 3, 4, and 5 years of treatment. We compared data between the groups according to the presence or absence of a virological response (VR) and resistance.

Results

Forty-eight patients were analyzed. There was no definite reduction in HBsAg level during the early period of treatment; differences in HBsAg levels between baseline and each time point were significant only at 5 years (P=0.028). In a subgroup analysis, this difference was significant only in non-resistant patients at 5 years (P=0.041).

Conclusions

There was no definite decrease in the HBsAg level during the early period of nucleoside analogue treatment, with long-term treatment being required to observe a significant reduction.

Citations

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  • Usefulness of a Hepatitis B Surface Antigen-Based Model for the Prediction of Functional Cure in Patients with Chronic Hepatitis B Virus Infection Treated with Nucleos(t)ide Analogues: A Real-World Study
    Gian Paolo Caviglia, Yulia Troshina, Enrico Garro, Marcantonio Gesualdo, Serena Aneli, Giovanni Birolo, Fabrizia Pittaluga, Rossana Cavallo, Giorgio Maria Saracco, Alessia Ciancio
    Journal of Clinical Medicine.2021; 10(15): 3308.     CrossRef
  • Tenofovir Disoproxil Fumarate Monotherapy is Superior to Entecavir-Adefovir Combination Therapy in Patients with Suboptimal Response to Lamivudine-Adefovir Therapy for Nucleoside-Resistant HBV: A 96-Week Prospective Multicentre Trial
    Sae Hwan Lee, Gab Jin Cheon, Hong Soo Kim, Sang Gyune Kim, Young Seok Kim, Soung Won Jeong, Jae Young Jang, Boo Sung Kim, Baek Gyu Jun, Young Don Kim, Dae Won Jun, Joo Hyun Sohn, Tae Yeob Kim, Byung Seok Lee
    Antiviral Therapy.2018; 23(3): 219.     CrossRef
  • Clinical Usefulness of HBsAg Quantification in Patients with Chronic Hepatitis B Infection
    Ergenekon Karagoz, Alpaslan Tanoglu
    Hepatitis Monthly.2017;[Epub]     CrossRef
  • Hepatitis B s antigen kinetics during treatment with nucleos(t)ides analogues in patients with hepatitis B e antigen‐negative chronic hepatitis B
    Athanasia Striki, Spilios Manolakopoulos, Melanie Deutsch, Anastasia Kourikou, George Kontos, Hariklia Kranidioti, Emilia Hadziyannis, George Papatheodoridis
    Liver International.2017; 37(11): 1642.     CrossRef
  • Pronounced decline of serum HBsAg in chronic hepatitis B patients with long-term effective nucleos(t)ide analogs therapy
    Meng-Lan Wang, En-Qiang Chen, Chuan-Min Tao, Tao-You Zhou, Juan Liao, Dong-Mei Zhang, Juan Wang, Hong Tang
    Scandinavian Journal of Gastroenterology.2017; 52(12): 1420.     CrossRef
  • Hepatitis B surface antigen levels at 6 months after treatment can predict the efficacy of lamivudine-adefovir combination therapy in patients with lamivudine-resistant chronic hepatitis B
    Jeong Han Kim, Hee Won Moon, Soon Young Ko, Won Hyeok Choe, So Young Kwon
    Clinical and Molecular Hepatology.2014; 20(3): 274.     CrossRef
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Viral hepatitis

Lamivudine plus adefovir combination therapy for lamivudine resistance in hepatitis-B-related hepatocellular carcinoma patients
Jeong Han Kim, Soon Young Ko, Won Hyeok Choe, So Young Kwon, Chang Hong Lee
Clin Mol Hepatol 2013;19(3):273-279.
Published online September 30, 2013
DOI: https://doi.org/10.3350/cmh.2013.19.3.273
Background/Aims

Lamivudine (LAM) plus adefovir (ADV) combination therapy has been accepted as one of the best treatments for LAM-resistant chronic hepatitis B (CHB). The aim of this study was to determine the efficacy of this combination therapy in hepatocellular carcinoma (HCC) patients.

Methods

The medical records of CHB patients who developed LAM resistance and were treated with LAM plus ADV combination therapy for more than 6 months were reviewed. Their virological response (VR; undetectable HBV DNA) and biochemical response (BR; alanine aminotransferase normalization) were evaluated, and the findings of HCC and non-HCC patients were compared.

Results

The data from 104 patients (19 with HCC and 85 without HCC) were analyzed. The VR rates did not differ significantly between the HCC and non-HCC groups: 33.3% vs. 55.6% at 12 months (P=0.119), 58.3% vs. 67.2% at 24 months (P=0.742), 50% vs. 69.8% at 36 months (P=0.280), and 66.7% vs. 71.0% at 48 months (P=1.000). The BR rates also did not differ significantly between the groups: 55.6% vs. 84.0% at 12 months (P=0.021), 58.3% vs. 83.8% at 24 months (P=0.057), 70.0% vs. 77.8% at 36 months (P=0.687), and 66.7% vs. 80.6% at 48 months (P=0.591).

Conclusions

The efficacy of LAM plus ADV combination therapy is comparable in HCC and non-HCC patients.

Citations

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  • Antiviral therapies for hepatitis B virus-related hepatocellular carcinoma
    Yuan-Qing Zhang
    World Journal of Gastroenterology.2015; 21(13): 3860.     CrossRef
  • 9,963 View
  • 44 Download
  • Crossref
Clinical features of acute viral hepatitis B in Korea: a multi-center study
Hye Jin Choi, Soon Young Ko, Won Hyeok Choe, Yeon Seok Seo, Ji Hoon Kim, Kwan Soo Byun, Young Seok Kim, Seung Up Kim, Soon Koo Baik, Jae Youn Cheong, Tae Yeob Kim, Oh Sang Kwon, Jeong Han Kim, Chang Hong Lee, So Young Kwon
Korean J Hepatol 2011;17(4):307-312.
Published online December 26, 2011
DOI: https://doi.org/10.3350/kjhep.2011.17.4.307
Background/Aims

The incidence of Hepatitis B has significantly declined since the introduction of an HBV vaccination program. The aim of this study was to investigate recent clinical features of acute viral hepatitis B (AVH-B) in Korea.

Methods

A total of 2241 patients with acute viral hepatitis were enrolled and their data were collected from nine medical-centers between January 2006 and December 2009.

Results

One hundred nineteen (5.3%) of the 2241 were diagnosed as AVH-B. Among 78 patients with AVH-B whose data were analyzed, 50 were male, and the mean age was 38.6 years. In an initial test, mean AST, ALT and total-bilirubin levels were 1296.2 IU/L, 2109.6 IU/L and 9.3 mg/dl, respectively. Positivity frequencies for HBeAg and anti-HBe were 55.1% and 67.9%, respectively, and the mean HBV DNA level was 5.2 log10 copies/ml. The mean length of hospitalization was 11.6 days. During follow-up, AST, ALT and total bilirubin levels were normalized or near-normalized in all patients without serious complications. Sixty-three of 66 (95.4%) patients showed HBsAg loss and 37 (56.1%) patients showed HBsAg seroconversion. Only 3 patients (4.5%) showed persistent hepatitis B viremia. There was no case of death or liver transplantation. Nine patients (11.3%) had received anti-viral agents and their clinical outcomes were not significantly different from those of patients treated without antiviral agents.

Conclusions

The prevalence of AVH-B among acute hepatitis patients is relatively low in Korea. AVH-B infection can be cured without complications in almost all patients, regardless of antiviral treatment.

Citations

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    Jung Hee Kim, Dong Hyun Sinn, Sung Wook Shin, Sung Ki Cho, Wonseok Kang, Geum-Youn Gwak, Yong-Han Paik, Joon Hyeok Lee, Kwang Cheol Koh, Seung Woon Paik, Moon Seok Choi
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    Yuan-Sheng Chen, Hui Zheng, Yan-Min Liu, Fu-Zhen Wang, Zhen-Hua Wu, Ning Miao, Xiao-Jin Sun, Guo-Min Zhang, Fu-Qiang Cui, Xiao-Feng Liang
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    Akinobu Tawada, Tatsuo Kanda, Fumio Imazeki, Osamu Yokosuka
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    Nisha Sharma, Mitchell S. Cappell
    Digestive Diseases and Sciences.2015; 60(9): 2590.     CrossRef
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    Jong Ho Lee, Sun Pyo Hong, Eun Sun Jang, Sang Jong Park, Seong Gyu Hwang, Sook‐Kyoung Kang, Sook‐Hyang Jeong
    Journal of Medical Virology.2015; 87(6): 993.     CrossRef
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    Hui Zheng, Fu-zhen Wang, Guo-min Zhang, Fu-qiang Cui, Zhen-hua Wu, Ning Miao, Xiao-jin Sun, Xiao-feng Liang, Li Li
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    So Young Kwon, Sang Hoon Park, Jong Eun Yeon, Sook Hyang Jeong, Oh Sang Kwon, Jin Woo Lee, Hong Soo Kim, Yeon Seok Seo, Young Seok Kim, Joo Hyun Sohn, Hyung Joon Yim, Jong Young Choi, Myung Seok Lee, Young Oh Kweon, Jae Youn Cheong, Haak Cheoul Kim, Heon
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