Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 30 (of 42 Records) |
Query Trace: Budd-chiari Syndrome[original query] |
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JAK2 mutations across a spectrum of venous thrombosis cases. American journal of clinical pathology 2010 Jul 134 (1): 82-5. Shetty Shrimati, Kulkarni Bipin, Pai Navin, Mukundan Preeti, Kasatkar Priyanka, Ghosh Kanjaks |
Association of factor VII gene polymorphisms with Budd Chiari syndrome. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2010 Apr 21 (3): 296-7. Jain Akriti, Shetty Shrimati, Kulkarni Bipin, Ghosh Kanjaks |
Hyperhomocysteinemia and the methylene tetrahydrofolate reductase C677T mutation in splanchnic vein thrombosis. European journal of haematology 2011 Feb 86 (2): 167-72. Vayá Amparo, Plumé Gema, Bonet Elena, Carrasco Paula, Morales-Suárez-Varela Maria |
The JAK2 46/1 haplotype in Budd-Chiari syndrome and portal vein thrombosis. Blood 2011 Apr 117 (15): 3968-73. Smalberg Jasper H, Koehler Edith, Darwish Murad Sarwa, Plessier Aurelie, Seijo Susana, Trebicka Jonel, Primignani Massimo, de Maat Moniek P M, Garcia-Pagan Juan-Carlos, Valla Dominique C, Janssen Harry L A, Leebeek Frank W G, |
Meta-analysis: the significance of screening for JAK2V617F mutation in Budd-Chiari syndrome and portal venous system thrombosis. Alimentary pharmacology & therapeutics 2011 May 33 (10): 1087-103. Qi X, Yang Z, Bai M, Shi X, Han G, Fan |
Prevalence of the JAK2V617F mutation in Chinese patients with Budd-Chiari syndrome and portal vein thrombosis: a prospective study. Journal of gastroenterology and hepatology 2012 Jun 27 (6): 1036-43. Qi Xingshun, Zhang Cheng, Han Guohong, Zhang Wei, He Chuangye, Yin Zhanxin, Liu Zhiwei, Bai Wei, Li Ruijun, Bai Ming, Yang Zhiping, Wu Kaichun, Fan Daimi |
Prevalence of JAK29V617F) mutation in intra-abdominal venous thrombosis. Tropical gastroenterology : official journal of the Digestive Diseases Foundation 0 32 (4): 279-84. Deepak Amarapurkar, Punamiya Sundeep, Patel Nikhil, Parekh Sunil, Mehta Shilpa, Shah Nira |
The clinical significance of JAK2V617F mutation for Philadelphia-negative chronic myeloproliferative neoplasms in patients with splanchnic vein thrombosis. Journal of thrombosis and thrombolysis 2012 Oct 34 (3): 388-96. Yonal Ipek, Pinarbas? Binnur, Hindilerden Fehmi, Hancer Veysel Sabri, Nalcaci Meliha, Kaymakoglu Sabahattin, Diz-Kucukkaya Reyh |
Prevalence and clinical outcomes of the 46/1 haplotype, Janus kinase 2 mutations, and ten-eleven translocation 2 mutations in Budd-Chiari syndrome and their impact on thrombotic complications post liver transplantation. Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society 2012 Jul 18 (7): 819-27. Westbrook Rachel H, Lea Nicholas C, Mohamedali Azim M, Smith Alexander E, Orr David W, Roberts Lara N, Heaton Nigel D, Wendon Julia A, O'Grady John G, Heneghan Michael A, Mufti Ghulam |
JAK2 V617F mutation and 46/1 haplotype in Chinese Budd-Chiari syndrome patients. Journal of gastroenterology and hepatology 2014 Jan 29 (1): 208-14. Wang Hui, Sun Guixiang, Zhang Peijin, Zhang Jing, Gui Er, Zu Maoheng, Jia Enzhi, Xu Hao, Xu Lichun, Zhang Jinpeng, Lu Zhaoj |
Thrombotic risk factors in Chinese Budd-Chiari syndrome patients. An observational study with a systematic review of the literature. Thrombosis and haemostasis 2013 May 109 (5): 878-84. Qi X, Wu F, Ren W, He C, Yin Z, Niu J, Bai M, Yang Z, Wu K, Fan D, Han |
Clinical features and etiology of Budd-Chiari syndrome in Chinese patients: a single-center study. Journal of gastroenterology and hepatology 2013 Jun 28 (6): 1061-7. Cheng Delei, Xu Hao, Lu Zhao-Jun, Hua Rong, Qiu Huan, Du Hongtao, Xu Xinjian, Zhang Ji |
Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT). Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2014 Sep 20 (6): 573-6. Pai Navin, Ghosh Kanjaksha, Shetty Shrima |
Role of calreticulin mutations in the aetiological diagnosis of splanchnic vein thrombosis. Journal of hepatology 2015 Jan 62 (1): 72-4. Turon Fanny, Cervantes Francisco, Colomer Dolors, Baiges Anna, Hernández-Gea Virginia, Garcia-Pagán Juan Carl |
Associations of coagulation factor V Leiden and prothrombin G20210A mutations with Budd-Chiari syndrome and portal vein thrombosis: a systematic review and meta-analysis. Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2014 Nov 12 (11): 1801-12.e7. Qi Xingshun, Ren Weirong, De Stefano Valerio, Fan Daimi |
Methylenetetrahydrofolate reductase C677T gene mutation and hyperhomocysteinemia in Budd-Chiari syndrome and portal vein thrombosis: A systematic review and meta-analysis of observational studies. Hepatology research : the official journal of the Japan Society of Hepatology 2014 Dec 44 (14): E480-98. Qi Xingshun, Yang Zhiping, De Stefano Valerio, Fan Daimi |
Risk of Budd-Chiari syndrome associated with factor V Leiden and G20210A prothrombin mutation: a meta-analysis. PloS one 2014 9 (4): e95719. Zhang Peijin, Zhang Jing, Sun Guixiang, Gao Xiuyin, Wang Hui, Yan Wenjun, Xu Hao, Zu Maoheng, Ma He, Wang Wei, Lu Zhaoj |
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. International journal of vascular medicine 2013 2013 717480. D'Amico Mario, Sammarco Pietro, Pasta Lin |
Association of factor V Leiden, Janus kinase 2, prothrombin, and MTHFR mutations with primary Budd-Chiari syndrome in Egyptian patients. Journal of gastroenterology and hepatology 2015 Aug . El Sebay Hatem M, Safan Manal A, Daoud Ashraf A, Tayel Safaa I, Nouh Alaa, El Shafie Shym |
Diagnostic value of the JAK2 V617F mutation for latent chronic myeloproliferative disorders in patients with Budd-Chiari syndrome and/or portal vein thrombosis. The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology 2015 Jan 26 (1): 42-8. Karaköse Süleyman, Oruç Nevin, Zengin Melia, Akarca Ulus Salih, Ersöz Gal |
PAI-1 4G-4G and MTHFR 677TT in non-hepatitis C virus/hepatitis B virus-related liver cirrhosis. World journal of hepatology 2015 Dec 7 (29): 2920-6. Pasta Linda, Pasta Frances |
Association between JAK2 rs4495487 Polymorphism and Risk of Budd-Chiari Syndrome in China. Gastroenterology research and practice 2015 2015 807865. Zhang Peijin, Zhang Yanyan, Zhang Jing, Wang Hui, Ma He, Wang Wei, Gao Xiuyin, Xu Hao, Lu Zhaoj |
Thrombophilia Profile in Budd-Chiari Syndrome and Splanchnic Vein Thrombosis: A Study from Western India. The Journal of the Association of Physicians of India 2015 Sep 63 (9): 32-5. Sawant Prabha, Vashishtha Chitranshu, Nasa Mukesh, Parikh Pathik, Patel Jignesh, Agasti Anan |
Investigation of Plasminogen Activator Inhibitor-1 (PAI-1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case-control study. European journal of haematology 2017 May . Prabhudesai Aniket, Shetty Shrimati, Ghosh Kanjaksha, Kulkarni Bip |
Prevalence of CALR mutations in splanchnic vein thrombosis: A systematic review and meta-analysis. Thrombosis research 2018 May 167 96-103. Li Miaomiao, De Stefano Valerio, Song Tingxue, Zhou Xinmiao, Guo Zeqi, Zhu Jia, Qi Xingsh |
Prevalence of prothrombotic factors in patients with Budd-Chiari syndrome or non-cirrhotic nonmalignant portal vein thrombosis: A hospital-based observational study. Journal of gastroenterology and hepatology 2019 11 35 (7): 1215-1222. Fan Jiahao, Wang Qiuhe, Luo Bohan, Chen Hui, Wang Zhengyu, Niu Jing, Yuan Jie, Yuan Xulong, Bai Wei, He Chuangye, Guo Wengang, Li Kai, Yin Zhanxin, Fan Daiming, Han Guoho |
Mutations in CYP2C9 and/or VKORC1 haplotype are associated with higher bleeding complications in patients with Budd-Chiari syndrome on warfarin. Hepatology international 2019 1 13 (2): 214-221. Shukla Akash, Jain Abhinav, Kahalekar Vinit, Bendkhale Sheetal, Gogtay Nithya, Thatte Urmila, Bhatia Shob |
Rivaroxaban for the treatment of noncirrhotic splanchnic vein thrombosis: an interventional prospective cohort study. Blood advances 2022 4 6 (12): 3569-3578. Ageno Walter, Beyer Westendorf Jan, Contino Laura, Bucherini Eugenio, Sartori Maria Teresa, Senzolo Marco, Grandone Elvira, Santoro Rita, Carrier Marc, Delluc Aurélien, De Stefano Valerio, Pomero Fulvio, Donadini Marco Paolo, Tosetto Alberto, Becattini Cecilia, Martinelli Ida, Nardo Barbara, Bertoletti Laurent, Di Nisio Marcello, Lazo-Langner Alejandro, Schenone Alessandro, Riva Nicolet |
Plasminogen Activator Inhibitor-1 4G/5G Promoter Polymorphism in Adults with Splanchnic Vein Thrombosis: A Case-Control Study. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2022 2 38 (1): 169-172. Kollabathula Arpitha, Sharma Saniya, Kumar Narender, Ahluwalia Jasmina, Das Reena, Varma Neelam, Rana Surinder Sin |
Prothrombotic states in portal vein thrombosis and Budd-Chiari syndrome in India: A systematic review and meta-analysis. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2023 8 . Suprabhat Giri, Sumaswi Angadi, Jijo Varghese, Sridhar Sundaram, Sukanya Bhrugumal |
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- Page last updated:Apr 29, 2024
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