Hepatic Dysfunction in Sickle Cell Disease: A New System of Classification Based on Global Assessment

Clinical Gastroenterology and Hepatology

Volumn 5, Issue 12, 2007, Pages 1469-1476

  Berry, Philip A ^a   Cross, Timothy J S ^a   Thein, Swee Lay ^a   Portmann, Bernard C ^a   Wendon, Julia A ^a   Karani, John B ^a   Heneghan, Michael A ^a   Bomford, Adrian ^a  

^a KING S COLLEGE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BETA THALASSEMIA; BILE DUCT DISEASE; BILE DUCT OBSTRUCTION; CHOLESTASIS; CLINICAL ARTICLE; CONTROLLED STUDY; DEMOGRAPHY; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DISEASE SEVERITY; FEMALE; FOLLOW UP; HUMAN; HUMAN TISSUE; LABORATORY TEST; LIVER BIOPSY; LIVER CIRRHOSIS; LIVER DYSFUNCTION; LIVER NECROSIS; MAGNETIC RESONANCE CHOLANGIOPANCREATOGRAPHY; MALE; SICKLE CELL ANEMIA; SIDEROSIS; VEIN BLOOD FLOW;

ADOLESCENT; ADULT; ANEMIA, SICKLE CELL; BIOPSY; CHOLANGIOGRAPHY; CHOLANGIOPANCREATOGRAPHY, ENDOSCOPIC RETROGRADE; DIAGNOSIS, DIFFERENTIAL; FEMALE; FOLLOW-UP STUDIES; HUMANS; LIVER; LIVER DISEASES; MALE; MIDDLE AGED; PROGNOSIS; RETROSPECTIVE STUDIES; SEVERITY OF ILLNESS INDEX; TOMOGRAPHY, X-RAY COMPUTED;

EID: 36549056944     PISSN: 15423565     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cgh.2007.08.009     Document Type: Article

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