Kulkarni B - Search Results

1

A common missense variant in exon 5 of antithrombin gene (SERPINC1) in Indian patients with thrombosis.

Deshpande R, Kulkarni B, Ghosh K, Shetty S. Deshpande R, et al. Among authors: kulkarni b. Thromb Res. 2016 Jul;143:1-2. doi: 10.1016/j.thromres.2016.04.012. Epub 2016 Apr 23. Thromb Res. 2016. PMID: 27161325 No abstract available.

2

Development of inhibitors in patients with haemophilia from India.

Ghosh K, Shetty S, Kulkarni B, Nair S, Pawar A, Khare A, Baindur S, Mohanty D. Ghosh K, et al. Among authors: kulkarni b. Haemophilia. 2001 May;7(3):273-8. doi: 10.1046/j.1365-2516.2001.00505.x. Haemophilia. 2001. PMID: 11380631

3

Frequency distribution of antigens in the human platelet antigen-1 system in the western Indian population.

Kulkarni B, Mohanty D, Ghosh K, Pawar A, Khare A. Kulkarni B, et al. Transfusion. 2002 Mar;42(3):317-20. doi: 10.1046/j.1537-2995.2002.00048.x. Transfusion. 2002. PMID: 11961236

4

Spectrum of inherited bleeding disorders from Western India.

Manisha M, Ghosh K, Shetty S, Nair S, Khare A, Kulkarni B, Pathare AV, Baindur S, Mohanty D. Manisha M, et al. Among authors: kulkarni b. Haematologia (Budap). 2002;32(1):39-47. doi: 10.1163/156855902760262754. Haematologia (Budap). 2002. PMID: 12243554

5

Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease.

Ghosh K, Kulkarni B, Nair S, Shetty S, Mohanty D. Ghosh K, et al. Among authors: kulkarni b. Br J Haematol. 2002 Nov;119(2):348-53. doi: 10.1046/j.1365-2141.2002.03864.x. Br J Haematol. 2002. PMID: 12406067 Free article.

6

Glanzmann's thrombasthenia: updated.

Nair S, Ghosh K, Kulkarni B, Shetty S, Mohanty D. Nair S, et al. Among authors: kulkarni b. Platelets. 2002 Nov;13(7):387-93. doi: 10.1080/0953710021000024394. Platelets. 2002. PMID: 12487785 Free article. Review.

7

Thrombophilia: hereditary and acquired in cardiovascular disease.

Khare A, Ghosh K, Kulkarni B, Mohanty D. Khare A, et al. Among authors: kulkarni b. Haematologia (Budap). 2002;32(4):293-311. Haematologia (Budap). 2002. PMID: 12803105 Review. No abstract available.

8

Inherited haemostatic disorders in idiopathic menorrhagia: do the special interest of a hemostatic laboratory make a difference?

Ghosh K, Nair S, Kulkarni B, Khare A, Trasi S, Shetty S, Mohanty D. Ghosh K, et al. Among authors: kulkarni b. Haemophilia. 2003 Sep;9(5):660-1. doi: 10.1046/j.1365-2516.2003.00798.x. Haemophilia. 2003. PMID: 14511314 No abstract available.

9

Milder bleeding tendency in Glanzmann's thrombasthenia patients inheriting HPA-1b in the homozygous state.

Ghosh K, Nair S, Kulkarni B, Shetty S, Mohanty D. Ghosh K, et al. Among authors: kulkarni b. J Thromb Haemost. 2003 Oct;1(10):2255-6. doi: 10.1046/j.1538-7836.2003.t01-3-00397.x. J Thromb Haemost. 2003. PMID: 14521621 Free article. No abstract available.

10

Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function.

Ghosh K, Nair S, Kulkarni B, Khare A, Shetty S, Mohanty D. Ghosh K, et al. Among authors: kulkarni b. Platelets. 2003 Sep;14(6):351-4. doi: 10.1080/09537100310001598792. Platelets. 2003. PMID: 14602548 Free article.

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