Budd-chiari Syndrome
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Last Posted: Aug 31, 2023
- Prothrombotic states in portal vein thrombosis and Budd-Chiari syndrome in India: A systematic review and meta-analysis.
Suprabhat Giri, et al. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2023 0 - Prevalence of prothrombotic factors in patients with Budd-Chiari syndrome or non-cirrhotic nonmalignant portal vein thrombosis: A hospital-based observational study.
Fan Jiahao, et al. Journal of gastroenterology and hepatology 2019 0 (7) 1215-1222 - Rivaroxaban for the treatment of noncirrhotic splanchnic vein thrombosis: an interventional prospective cohort study.
Ageno Walter, et al. Blood advances 2022 0 (12) 3569-3578 - Mutations in CYP2C9 and/or VKORC1 haplotype are associated with higher bleeding complications in patients with Budd-Chiari syndrome on warfarin.
Shukla Akash, et al. Hepatology international 2019 0 (2) 214-221 - [Relationship between factor v Leiden mutation and Chinese Budd-Chiari syndrome and its clinical significance].
Feng B, et al. Zhonghua yi xue za zhi 2002 0 (5) 354-7 - Plasminogen Activator Inhibitor-1 4G/5G Promoter Polymorphism in Adults with Splanchnic Vein Thrombosis: A Case-Control Study.
Kollabathula Arpitha, et al. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2022 0 (1) 169-172 - Vascular diseases of the liver. Clinical Guidelines from the Catalan Society of Digestology and the Spanish Association for the Study of the Liver.
Martín-Llahí Marta et al. Gastroenterologia y hepatologia 2017 Oct 40(8) 538-580 - Prevalence of CALR mutations in splanchnic vein thrombosis: A systematic review and meta-analysis.
Li Miaomiao, et al. Thrombosis research 2018 5 96-103 - Investigation of Plasminogen Activator Inhibitor-1 (PAI-1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case-control study.
Prabhudesai Aniket, et al. European journal of haematology 2017 5 - Thrombophilia Profile in Budd-Chiari Syndrome and Splanchnic Vein Thrombosis: A Study from Western India.
Sawant Prabha, et al. The Journal of the Association of Physicians of India 2015 9 (9) 32-5 - PAI-1 4G-4G and MTHFR 677TT in non-hepatitis C virus/hepatitis B virus-related liver cirrhosis.
Pasta Linda, et al. World journal of hepatology 2015 12 (29) 2920-6 - Association between JAK2 rs4495487 Polymorphism and Risk of Budd-Chiari Syndrome in China.
Zhang Peijin, et al. Gastroenterology research and practice 2015 0 807865 - Association of factor V Leiden, Janus kinase 2, prothrombin, and MTHFR mutations with primary Budd-Chiari syndrome in Egyptian patients.
El Sebay Hatem M, et al. Journal of gastroenterology and hepatology 2015 8 - Role of calreticulin mutations in the aetiological diagnosis of splanchnic vein thrombosis.
Turon Fanny, et al. Journal of hepatology 2015 1 (1) 72-4 - Diagnostic value of the JAK2 V617F mutation for latent chronic myeloproliferative disorders in patients with Budd-Chiari syndrome and/or portal vein thrombosis.
Karaköse Süleyman, et al. The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology 2015 1 (1) 42-8 - Associations of coagulation factor V Leiden and prothrombin G20210A mutations with Budd-Chiari syndrome and portal vein thrombosis: a systematic review and meta-analysis.
Qi Xingshun, et al. Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2014 11 (11) 1801-12.e7 - Methylenetetrahydrofolate reductase C677T gene mutation and hyperhomocysteinemia in Budd-Chiari syndrome and portal vein thrombosis: A systematic review and meta-analysis of observational studies.
Qi Xingshun, et al. Hepatology research : the official journal of the Japan Society of Hepatology 2014 12 (14) E480-98 - Risk of Budd-Chiari syndrome associated with factor V Leiden and G20210A prothrombin mutation: a meta-analysis.
Zhang Peijin, et al. PloS one 2014 0 (4) e95719 - Thrombophilic Genetic Factors PAI-1, MTHFRC677T, V Leiden 506Q, and Prothrombin 20210A in Noncirrhotic Portal Vein Thrombosis and Budd-Chiari Syndrome in a Caucasian Population.
D'Amico Mario, et al. International journal of vascular medicine 2013 0 717480 - JAK2 V617F mutation and 46/1 haplotype in Chinese Budd-Chiari syndrome patients.
Wang Hui, et al. Journal of gastroenterology and hepatology 2014 1 (1) 208-14
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- Page last reviewed:Feb 1, 2024
- Page last updated:May 18, 2024
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