Condition: Budd-Chiari Syndrome


rs77375493 in INSL6;JAK2 gene and Budd-Chiari Syndrome PMID 25698270 2015 Diagnostic value of the JAK2 V617F mutation for latent chronic myeloproliferative disorders in patients with Budd-Chiari syndrome and/or portal vein thrombosis.

PMID 18600100 2008 Determination of the JAK2 V617F mutation may be useful to recognize patients with Budd-Chiari syndrome with or at risk for the subsequent development of overt myeloproliferative diseases.

PMID 16762626 2006 Prevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome.

PMID 19293426 2009 The presence of JAK2V617F mutation in the liver endothelial cells of patients with Budd-Chiari syndrome.

PMID 23425079 2013 Clinical features and etiology of Budd-Chiari syndrome in Chinese patients: a single-center study.

PMID 23980667 2014 JAK2 V617F mutation and 46/1 haplotype in Chinese Budd-Chiari syndrome patients.