Pai N - Search Results

1

JAK2 mutations across a spectrum of venous thrombosis cases.

Shetty S, Kulkarni B, Pai N, Mukundan P, Kasatkar P, Ghosh K. Shetty S, et al. Among authors: pai n. Am J Clin Pathol. 2010 Jul;134(1):82-5. doi: 10.1309/AJCP7VO4HAIZYATP. Am J Clin Pathol. 2010. PMID: 20551270

2

Differences in etiological and clinical manifestations in upper extremity and lower limb deep venous thrombosis patients from India.

Pai N, Shetty S, Kulkarni B, Ghosh K. Pai N, et al. Clin Appl Thromb Hemost. 2010 Dec;16(6):698-700. doi: 10.1177/1076029609351290. Epub 2009 Nov 10. Clin Appl Thromb Hemost. 2010. PMID: 19903694 Free article.

3

Cause of deep venous thrombosis and pulmonary embolism in young patients from India as compared with other ethnic groups.

Pai N, Ghosh K, Shetty S. Pai N, et al. Blood Coagul Fibrinolysis. 2012 Jun;23(4):257-61. doi: 10.1097/MBC.0b013e3283502961. Blood Coagul Fibrinolysis. 2012. PMID: 22498980

4

Hereditary protein C deficiency in Indian patients with venous thrombosis.

Pai N, Ghosh K, Shetty S. Pai N, et al. Ann Hematol. 2012 Sep;91(9):1471-6. doi: 10.1007/s00277-012-1483-5. Epub 2012 May 11. Ann Hematol. 2012. PMID: 22576310

5

Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT).

Pai N, Ghosh K, Shetty S. Pai N, et al. Clin Appl Thromb Hemost. 2014 Sep;20(6):573-6. doi: 10.1177/1076029613476339. Epub 2013 Feb 12. Clin Appl Thromb Hemost. 2014. PMID: 23406614 Free article. Clinical Trial.

6

Hereditary thrombophilia in cerebral venous thrombosis: a study from India.

Pai N, Ghosh K, Shetty S. Pai N, et al. Blood Coagul Fibrinolysis. 2013 Jul;24(5):540-3. doi: 10.1097/MBC.0b013e32835fad1e. Blood Coagul Fibrinolysis. 2013. PMID: 23518830

7

Prenatal diagnosis in a family with purfura fulminans.

Shanbhag S, Pai N, Ghosh K, Shetty S. Shanbhag S, et al. Among authors: pai n. Blood Coagul Fibrinolysis. 2015 Apr;26(3):350. doi: 10.1097/MBC.0000000000000251. Blood Coagul Fibrinolysis. 2015. PMID: 25803516 No abstract available.

8

Hereditary basis of protein C deficiency (PCD) in thrombosis patients: first report from India.

Pai N, Shetty S, Idicula-Thomas S, Kulkarni B, Ghosh K. Pai N, et al. Thromb Haemost. 2009 Apr;101(4):785-7. Thromb Haemost. 2009. PMID: 19350130 No abstract available.

9

Absence of Protein C Sapporo in Indian Patients With Venous Thrombosis.

Pai N, Shetty SD, Ghosh K. Pai N, et al. Clin Appl Thromb Hemost. 2009 Apr 28. doi: 10.1177/1076029609333675. Online ahead of print. Clin Appl Thromb Hemost. 2009. PMID: 19403521 No abstract available.

10

Protein C (PROC) gene mutations in two Indian families with purpura fulminans.

Pai N, Shetty S, Ghosh K. Pai N, et al. Ann Hematol. 2010 Aug;89(8):835-6. doi: 10.1007/s00277-009-0893-5. Epub 2010 Jan 14. Ann Hematol. 2010. PMID: 20077116 No abstract available.

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