Literature DB >> 29616413

Prothrombin gene mutation in Budd-Chiari syndrome-The first case report from India.

Abhinav Jain1, Akash Shukla2.   

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Year:  2018        PMID: 29616413     DOI: 10.1007/s12664-018-0845-x

Source DB:  PubMed          Journal:  Indian J Gastroenterol        ISSN: 0254-8860


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  10 in total

1.  Low frequency of factor V Leiden and prothrombin G20210A mutations in patients with hepatic venous outflow tract obstruction in northern India: a case-control study.

Authors:  Sirish I Kumar; Ashish Kumar; Srikant Srivastava; Vivek A Saraswat; Rakesh Aggarwal
Journal:  Indian J Gastroenterol       Date:  2005 Sep-Oct

2.  A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

Authors:  S R Poort; F R Rosendaal; P H Reitsma; R M Bertina
Journal:  Blood       Date:  1996-11-15       Impact factor: 22.113

3.  Clinical and prothrombotic profile of hepatic vein outflow tract obstruction.

Authors:  Seema Alam; Rajeev Khanna; Amar Mukund
Journal:  Indian J Pediatr       Date:  2013-07-25       Impact factor: 1.967

4.  G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men.

Authors:  P M Ridker; C H Hennekens; J P Miletich
Journal:  Circulation       Date:  1999-03-02       Impact factor: 29.690

5.  Hereditary and Acquired Thrombophilia in Splanchnic Vein Thrombosis: A Single-Center Experience.

Authors:  Deepti Mutreja; Mrinalini Kotru; Sudha Sazawal; Ravi Ranjan; Amit Sharma; Subrat Kumar Acharya; Renu Saxena
Journal:  Clin Appl Thromb Hemost       Date:  2013-11-19       Impact factor: 2.389

Review 6.  Budd-Chiari syndrome/hepatic venous outflow tract obstruction.

Authors:  Dominique-Charles Valla
Journal:  Hepatol Int       Date:  2017-07-06       Impact factor: 6.047

7.  Hereditary thrombophilia as a cause of Budd-Chiari syndrome: a study from Western India.

Authors:  D Mohanty; S Shetty; K Ghosh; A Pawar; P Abraham
Journal:  Hepatology       Date:  2001-10       Impact factor: 17.425

8.  Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis: a study from North India.

Authors:  Maitreyee Bhattacharyya; Govind Makharia; M Kannan; R P H Ahmed; P K Gupta; Renu Saxena
Journal:  Am J Clin Pathol       Date:  2004-06       Impact factor: 2.493

9.  Changing spectrum of Budd-Chiari syndrome in India with special reference to non-surgical treatment.

Authors:  Deepak N Amarapurkar; Sundeep J Punamiya; Nikhil D Patel
Journal:  World J Gastroenterol       Date:  2008-01-14       Impact factor: 5.742

10.  Risk of Budd-Chiari syndrome associated with factor V Leiden and G20210A prothrombin mutation: a meta-analysis.

Authors:  Peijin Zhang; Jing Zhang; Guixiang Sun; Xiuyin Gao; Hui Wang; Wenjun Yan; Hao Xu; Maoheng Zu; He Ma; Wei Wang; Zhaojun Lu
Journal:  PLoS One       Date:  2014-04-22       Impact factor: 3.240

  10 in total
  1 in total

Review 1.  An Update on the Management of Budd-Chiari Syndrome.

Authors:  A Sharma; S N Keshava; A Eapen; E Elias; C E Eapen
Journal:  Dig Dis Sci       Date:  2020-07-20       Impact factor: 3.199

  1 in total

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