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Bipin Kulkarni

Showing results (1-10 of 22) with videos related to

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Transfusion|August 24, 2017
A novel homozygous frameshift mutation in Exon 7 of the ADAMTS13 gene in a patient with congenital thrombotic thrombocytopenic purpura from India: a case reportSneha Yadav, Shrimati Shetty, Bipin Kulkarni
The Journal of the Association of Physicians of India|October 21, 2018
Multiple Heritable and Acquired Risk Factors in a Case of Recurrent Retinal Vein OcclusionAniket Prabhudesai, Shrimati Shetty, Kanjaksha Ghosh, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|November 12, 2009
Differences in etiological and clinical manifestations in upper extremity and lower limb deep venous thrombosis patients from IndiaNavin Pai, Shrimati Shetty, Bipin Kulkarni, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 8, 2008
Spectrum of changes in endogenous thrombin potential due to heritable disorders of coagulationKanjaksha Ghosh, Leenam Mota, Shrimati Shetty, et al.
Blood Cells, Molecules & Diseases|May 30, 2017
Dysfunctional fibrinolysis and cerebral venous thrombosisAniket Prabhudesai, Shrimati Shetty, Kanjaksha Ghosh, et al.
European Journal of Haematology|June 1, 2017
Investigation of Plasminogen Activator Inhibitor-1 (PAI-1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case-control studyAniket Prabhudesai, Shrimati Shetty, Kanjaksha Ghosh, et al.
Prenatal Diagnosis|August 15, 2008
Utility of an exon 14 BslI polymorphism for improved genetic diagnosis of hemophilia A in Indian populationPreethi Mukundan, Shrimati Shetty, Bipin Kulkarni, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 2010
Molecular pathology of haemophilia A in Indian patients: identification of 11 novel mutationsPreethi Satish Nair, Shrimati Shetty, Bipin Kulkarni, et al.
British Journal of Haematology|October 31, 2002
Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the diseaseKanjaksha Ghosh, Bipin Kulkarni, Sona Nair, et al.
Indian Journal of Medical Sciences|October 8, 2004
Combination of thrombophilia markers in acute myocardial infarction of the youngAmit Khare, Kanjaksha Ghosh, Shrimati Shetty, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Transfusion|August 24, 2017
A novel homozygous frameshift mutation in Exon 7 of the ADAMTS13 gene in a patient with congenital thrombotic thrombocytopenic purpura from India: a case reportSneha Yadav, Shrimati Shetty, Bipin Kulkarni
The Journal of the Association of Physicians of India|October 21, 2018
Multiple Heritable and Acquired Risk Factors in a Case of Recurrent Retinal Vein OcclusionAniket Prabhudesai, Shrimati Shetty, Kanjaksha Ghosh, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|November 12, 2009
Differences in etiological and clinical manifestations in upper extremity and lower limb deep venous thrombosis patients from IndiaNavin Pai, Shrimati Shetty, Bipin Kulkarni, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 8, 2008
Spectrum of changes in endogenous thrombin potential due to heritable disorders of coagulationKanjaksha Ghosh, Leenam Mota, Shrimati Shetty, et al.
Blood Cells, Molecules & Diseases|May 30, 2017
Dysfunctional fibrinolysis and cerebral venous thrombosisAniket Prabhudesai, Shrimati Shetty, Kanjaksha Ghosh, et al.
European Journal of Haematology|June 1, 2017
Investigation of Plasminogen Activator Inhibitor-1 (PAI-1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case-control studyAniket Prabhudesai, Shrimati Shetty, Kanjaksha Ghosh, et al.
Prenatal Diagnosis|August 15, 2008
Utility of an exon 14 BslI polymorphism for improved genetic diagnosis of hemophilia A in Indian populationPreethi Mukundan, Shrimati Shetty, Bipin Kulkarni, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 2010
Molecular pathology of haemophilia A in Indian patients: identification of 11 novel mutationsPreethi Satish Nair, Shrimati Shetty, Bipin Kulkarni, et al.
British Journal of Haematology|October 31, 2002
Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the diseaseKanjaksha Ghosh, Bipin Kulkarni, Sona Nair, et al.
Indian Journal of Medical Sciences|October 8, 2004
Combination of thrombophilia markers in acute myocardial infarction of the youngAmit Khare, Kanjaksha Ghosh, Shrimati Shetty, et al.
Pageof 3