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Non-cirrhotic Intrahepatic Portal Hypertension: Associated Gut Diseases and Prognostic Factors
Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH....
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Published in: | Digestive diseases and sciences 2011-01, Vol.56 (1), p.227-235 |
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description | Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH. Methods We retrospectively analyzed prognostic indicators in 34 NCIPH patients. We also searched for associated gut diseases. Results Transplant-free survival in NCIPH patients from first presentation with NCIPH at 1, 5, and 10 years was 94% (SE: 4.2%), 84% (6.6%), and 69% (9.8%), respectively. Decompensated liver disease occurred in 53% of patients. Three (9%) patients had ulcerative colitis while five of 31 (16%) tested had celiac disease and on Kaplan-Meier analysis, celiac disease predicted reduced transplant-free survival (p = 0.018). On multivariable Cox regression analysis, independent predictors of reduced transplant-free survival were older age at first presentation with NCIPH, hepatic encephalopathy, and portal vein thrombosis. Prevalence of elevated initial serum IgA anticardiolipin antibody (CLPA) was significantly higher in NCIPH (36% of patients tested), compared to Budd-Chiari syndrome (6%) (p = 0.032, Fisher's exact test) and celiac disease without concomitant liver disease (0%) (p = 0.007). Conclusions We have identified prognostic factors and report progression to liver failure in 53% of NCIPH patients followed-up at our center. Our data supports a role for intestinal disease in the pathogenesis of intrahepatic portal vein occlusion leading to NCIPH. |
doi_str_mv | 10.1007/s10620-010-1278-2 |
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E ; Nightingale, Peter ; Hubscher, Stefan G ; Lane, Peter J ; Plant, Timothy ; Velissaris, Dimitris ; Elias, Elwyn</creator><creatorcontrib>Eapen, C. E ; Nightingale, Peter ; Hubscher, Stefan G ; Lane, Peter J ; Plant, Timothy ; Velissaris, Dimitris ; Elias, Elwyn</creatorcontrib><description>Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH. Methods We retrospectively analyzed prognostic indicators in 34 NCIPH patients. We also searched for associated gut diseases. Results Transplant-free survival in NCIPH patients from first presentation with NCIPH at 1, 5, and 10 years was 94% (SE: 4.2%), 84% (6.6%), and 69% (9.8%), respectively. Decompensated liver disease occurred in 53% of patients. Three (9%) patients had ulcerative colitis while five of 31 (16%) tested had celiac disease and on Kaplan-Meier analysis, celiac disease predicted reduced transplant-free survival (p = 0.018). On multivariable Cox regression analysis, independent predictors of reduced transplant-free survival were older age at first presentation with NCIPH, hepatic encephalopathy, and portal vein thrombosis. Prevalence of elevated initial serum IgA anticardiolipin antibody (CLPA) was significantly higher in NCIPH (36% of patients tested), compared to Budd-Chiari syndrome (6%) (p = 0.032, Fisher's exact test) and celiac disease without concomitant liver disease (0%) (p = 0.007). Conclusions We have identified prognostic factors and report progression to liver failure in 53% of NCIPH patients followed-up at our center. Our data supports a role for intestinal disease in the pathogenesis of intrahepatic portal vein occlusion leading to NCIPH.</description><identifier>ISSN: 0163-2116</identifier><identifier>EISSN: 1573-2568</identifier><identifier>DOI: 10.1007/s10620-010-1278-2</identifier><identifier>PMID: 20499175</identifier><identifier>CODEN: DDSCDJ</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Analysis ; Antibodies, Anticardiolipin - blood ; Anticardiolipin antibodies ; Biochemistry ; Biological and medical sciences ; Biopsy ; Celiac Disease - diagnosis ; Celiac Disease - epidemiology ; Celiac Disease - mortality ; Cohort Studies ; Colitis, Ulcerative - diagnosis ; Colitis, Ulcerative - epidemiology ; Colitis, Ulcerative - mortality ; Comorbidity ; Feeding. Feeding behavior ; Female ; Follow-Up Studies ; Fundamental and applied biological sciences. Psychology ; Gastroenterology ; Gastroenterology. Liver. Pancreas. Abdomen ; Hepatology ; Humans ; Hypertension, Portal - diagnosis ; Hypertension, Portal - epidemiology ; Hypertension, Portal - mortality ; Immunoglobulin A ; Kaplan-Meier Estimate ; Liver ; Liver - pathology ; Liver cirrhosis ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Lupus Coagulation Inhibitor - blood ; Male ; Medical research ; Medical sciences ; Medicine ; Medicine & Public Health ; Medicine, Experimental ; Middle Aged ; Oncology ; Original Article ; Other diseases. Semiology ; Portal hypertension ; Prognosis ; Regression Analysis ; Retrospective Studies ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Survival Rate ; Transplant Surgery ; Ulcerative colitis ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Young Adult</subject><ispartof>Digestive diseases and sciences, 2011-01, Vol.56 (1), p.227-235</ispartof><rights>Springer Science+Business Media, LLC 2010</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2011 Springer</rights><rights>Springer Science+Business Media, LLC 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c590t-27d76ac04d7d9394bc56e25371a0ce6941936dcb7c61d35b97a0a3ddf7b88b6c3</citedby><cites>FETCH-LOGICAL-c590t-27d76ac04d7d9394bc56e25371a0ce6941936dcb7c61d35b97a0a3ddf7b88b6c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23838137$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20499175$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eapen, C. E</creatorcontrib><creatorcontrib>Nightingale, Peter</creatorcontrib><creatorcontrib>Hubscher, Stefan G</creatorcontrib><creatorcontrib>Lane, Peter J</creatorcontrib><creatorcontrib>Plant, Timothy</creatorcontrib><creatorcontrib>Velissaris, Dimitris</creatorcontrib><creatorcontrib>Elias, Elwyn</creatorcontrib><title>Non-cirrhotic Intrahepatic Portal Hypertension: Associated Gut Diseases and Prognostic Factors</title><title>Digestive diseases and sciences</title><addtitle>Dig Dis Sci</addtitle><addtitle>Dig Dis Sci</addtitle><description>Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH. Methods We retrospectively analyzed prognostic indicators in 34 NCIPH patients. We also searched for associated gut diseases. Results Transplant-free survival in NCIPH patients from first presentation with NCIPH at 1, 5, and 10 years was 94% (SE: 4.2%), 84% (6.6%), and 69% (9.8%), respectively. Decompensated liver disease occurred in 53% of patients. Three (9%) patients had ulcerative colitis while five of 31 (16%) tested had celiac disease and on Kaplan-Meier analysis, celiac disease predicted reduced transplant-free survival (p = 0.018). On multivariable Cox regression analysis, independent predictors of reduced transplant-free survival were older age at first presentation with NCIPH, hepatic encephalopathy, and portal vein thrombosis. Prevalence of elevated initial serum IgA anticardiolipin antibody (CLPA) was significantly higher in NCIPH (36% of patients tested), compared to Budd-Chiari syndrome (6%) (p = 0.032, Fisher's exact test) and celiac disease without concomitant liver disease (0%) (p = 0.007). Conclusions We have identified prognostic factors and report progression to liver failure in 53% of NCIPH patients followed-up at our center. Our data supports a role for intestinal disease in the pathogenesis of intrahepatic portal vein occlusion leading to NCIPH.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Analysis</subject><subject>Antibodies, Anticardiolipin - blood</subject><subject>Anticardiolipin antibodies</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Celiac Disease - diagnosis</subject><subject>Celiac Disease - epidemiology</subject><subject>Celiac Disease - mortality</subject><subject>Cohort Studies</subject><subject>Colitis, Ulcerative - diagnosis</subject><subject>Colitis, Ulcerative - epidemiology</subject><subject>Colitis, Ulcerative - mortality</subject><subject>Comorbidity</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenterology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Hypertension, Portal - diagnosis</subject><subject>Hypertension, Portal - epidemiology</subject><subject>Hypertension, Portal - mortality</subject><subject>Immunoglobulin A</subject><subject>Kaplan-Meier Estimate</subject><subject>Liver</subject><subject>Liver - pathology</subject><subject>Liver cirrhosis</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Lupus Coagulation Inhibitor - blood</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Medicine, Experimental</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Other diseases. Semiology</subject><subject>Portal hypertension</subject><subject>Prognosis</subject><subject>Regression Analysis</subject><subject>Retrospective Studies</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Survival Rate</subject><subject>Transplant Surgery</subject><subject>Ulcerative colitis</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Young Adult</subject><issn>0163-2116</issn><issn>1573-2568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kU1v1DAQhiMEokvhB3CBCITgkjJjJ3bMbVXoh1RBJegVy7GdrausvbWTQ_89jrJQgVDlgz32886M3ymKlwhHCMA_JgRGoAKECglvK_KoWGHDaUUa1j4uVoAsnxHZQfEspRsAEBzZ0-KAQC0E8mZV_PwafKVdjNdhdLo892NU13an5uAyxFEN5dndzsbR-uSC_1SuUwraqdGa8nQay88uWZVsKpU35WUMGx_SrD1RegwxPS-e9GpI9sV-PyyuTr78OD6rLr6dnh-vLyrdCBgrwg1nSkNtuBFU1J1umCUN5ahAWyZqFJQZ3XHN0NCmE1yBosb0vGvbjml6WLxf8u5iuJ1sGuXWJW2HQXkbpiTb7IIQ2ahMfniQxFyMNpwgyeibf9CbMEWf_5HzQQvZWJahtwu0UYOVzvchO6jnnHLNkYhaMFJn6ug_VF7Gbp0O3vYu3_8lwEWgY0gp2l7uotuqeCcR5Dx8uQxfwhzn4cu531f7fqdua80fxe9pZ-DdHlBJq6GPymuX7jna0hYpzxxZuJSf_MbG-48_VP31IupVkGoTc-Kr7wSQAgqCLQD9BRj4zVY</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Eapen, C. E</creator><creator>Nightingale, Peter</creator><creator>Hubscher, Stefan G</creator><creator>Lane, Peter J</creator><creator>Plant, Timothy</creator><creator>Velissaris, Dimitris</creator><creator>Elias, Elwyn</creator><general>Boston : Springer US</general><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20110101</creationdate><title>Non-cirrhotic Intrahepatic Portal Hypertension: Associated Gut Diseases and Prognostic Factors</title><author>Eapen, C. E ; Nightingale, Peter ; Hubscher, Stefan G ; Lane, Peter J ; Plant, Timothy ; Velissaris, Dimitris ; Elias, Elwyn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c590t-27d76ac04d7d9394bc56e25371a0ce6941936dcb7c61d35b97a0a3ddf7b88b6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Analysis</topic><topic>Antibodies, Anticardiolipin - blood</topic><topic>Anticardiolipin antibodies</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Celiac Disease - diagnosis</topic><topic>Celiac Disease - epidemiology</topic><topic>Celiac Disease - mortality</topic><topic>Cohort Studies</topic><topic>Colitis, Ulcerative - diagnosis</topic><topic>Colitis, Ulcerative - epidemiology</topic><topic>Colitis, Ulcerative - mortality</topic><topic>Comorbidity</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenterology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Hypertension, Portal - diagnosis</topic><topic>Hypertension, Portal - epidemiology</topic><topic>Hypertension, Portal - mortality</topic><topic>Immunoglobulin A</topic><topic>Kaplan-Meier Estimate</topic><topic>Liver</topic><topic>Liver - pathology</topic><topic>Liver cirrhosis</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Lupus Coagulation Inhibitor - blood</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Medicine, Experimental</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Other diseases. Semiology</topic><topic>Portal hypertension</topic><topic>Prognosis</topic><topic>Regression Analysis</topic><topic>Retrospective Studies</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Survival Rate</topic><topic>Transplant Surgery</topic><topic>Ulcerative colitis</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eapen, C. E</creatorcontrib><creatorcontrib>Nightingale, Peter</creatorcontrib><creatorcontrib>Hubscher, Stefan G</creatorcontrib><creatorcontrib>Lane, Peter J</creatorcontrib><creatorcontrib>Plant, Timothy</creatorcontrib><creatorcontrib>Velissaris, Dimitris</creatorcontrib><creatorcontrib>Elias, Elwyn</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Hospital Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Databases</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Digestive diseases and sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eapen, C. E</au><au>Nightingale, Peter</au><au>Hubscher, Stefan G</au><au>Lane, Peter J</au><au>Plant, Timothy</au><au>Velissaris, Dimitris</au><au>Elias, Elwyn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Non-cirrhotic Intrahepatic Portal Hypertension: Associated Gut Diseases and Prognostic Factors</atitle><jtitle>Digestive diseases and sciences</jtitle><stitle>Dig Dis Sci</stitle><addtitle>Dig Dis Sci</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>56</volume><issue>1</issue><spage>227</spage><epage>235</epage><pages>227-235</pages><issn>0163-2116</issn><eissn>1573-2568</eissn><coden>DDSCDJ</coden><abstract>Background/Aims Non-cirrhotic intrahepatic portal hypertension (NCIPH) is generally regarded to have a benign prognosis. We have studied a cohort followed-up at a tertiary referral center and postulate that gut-derived prothrombotic factors may contribute to the pathogenesis and prognosis of NCIPH. Methods We retrospectively analyzed prognostic indicators in 34 NCIPH patients. We also searched for associated gut diseases. Results Transplant-free survival in NCIPH patients from first presentation with NCIPH at 1, 5, and 10 years was 94% (SE: 4.2%), 84% (6.6%), and 69% (9.8%), respectively. Decompensated liver disease occurred in 53% of patients. Three (9%) patients had ulcerative colitis while five of 31 (16%) tested had celiac disease and on Kaplan-Meier analysis, celiac disease predicted reduced transplant-free survival (p = 0.018). On multivariable Cox regression analysis, independent predictors of reduced transplant-free survival were older age at first presentation with NCIPH, hepatic encephalopathy, and portal vein thrombosis. Prevalence of elevated initial serum IgA anticardiolipin antibody (CLPA) was significantly higher in NCIPH (36% of patients tested), compared to Budd-Chiari syndrome (6%) (p = 0.032, Fisher's exact test) and celiac disease without concomitant liver disease (0%) (p = 0.007). Conclusions We have identified prognostic factors and report progression to liver failure in 53% of NCIPH patients followed-up at our center. Our data supports a role for intestinal disease in the pathogenesis of intrahepatic portal vein occlusion leading to NCIPH.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>20499175</pmid><doi>10.1007/s10620-010-1278-2</doi><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Analysis Antibodies, Anticardiolipin - blood Anticardiolipin antibodies Biochemistry Biological and medical sciences Biopsy Celiac Disease - diagnosis Celiac Disease - epidemiology Celiac Disease - mortality Cohort Studies Colitis, Ulcerative - diagnosis Colitis, Ulcerative - epidemiology Colitis, Ulcerative - mortality Comorbidity Feeding. Feeding behavior Female Follow-Up Studies Fundamental and applied biological sciences. Psychology Gastroenterology Gastroenterology. Liver. Pancreas. Abdomen Hepatology Humans Hypertension, Portal - diagnosis Hypertension, Portal - epidemiology Hypertension, Portal - mortality Immunoglobulin A Kaplan-Meier Estimate Liver Liver - pathology Liver cirrhosis Liver. Biliary tract. Portal circulation. Exocrine pancreas Lupus Coagulation Inhibitor - blood Male Medical research Medical sciences Medicine Medicine & Public Health Medicine, Experimental Middle Aged Oncology Original Article Other diseases. Semiology Portal hypertension Prognosis Regression Analysis Retrospective Studies Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Survival Rate Transplant Surgery Ulcerative colitis Vertebrates: anatomy and physiology, studies on body, several organs or systems Young Adult |
title | Non-cirrhotic Intrahepatic Portal Hypertension: Associated Gut Diseases and Prognostic Factors |
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