495 results on '"Shetty, Shrimati"'
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2. A novel SERPINC1 c.119G>A (p.Cys40Tyr) mutation with variable clinical expression in an Indian family
3. Mortality in Haemophilia Patients in India: A National Cohort Study.
4. Successful Treatment Of Acquired Hemophilia A Using FEIBA Supplemented With Emicizumab
5. Differential response to FEIBA is strongly associated with the prothrombotic microparticles
6. Indian Society of Hematology and Blood Transfusion (ISHBT) Consensus Document on Hematological Practice During COVID-19 Pandemic
7. Association of Thrombophilic Factors in Pathogenesis of Osteonecrosis of Femoral Head in Indian Population
8. Prediction of preeclampsia using combination of biomarkers at 18–23 weeks of gestation: A nested case-control study
9. Role of lupus anticoagulants in immediate acting inhibitor positivity in congenital haemophilia A patients
10. Combination of copeptin, placental growth factor and total annexin V microparticles for prediction of preeclampsia at 10–14 weeks of gestation
11. Dysfunctional fibrinolysis and cerebral venous thrombosis
12. Bengal macrothrombocytopenia is not totally an innocuous condition
13. F8 gene mutation profile in Indian hemophilia A patients: Identification of 23 novel mutations and factor VIII inhibitor risk association
14. Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations
15. Epidemiology of hepatocellular carcinoma (HCC) in hemophilia
16. Antibody profile in Indian severe haemophilia A patients with and without FVIII inhibitors
17. Differential expression of genes involved in Bengal macrothrombocytopenia (BMTCP)
18. Inherited and acquired thrombophilia in Indian women experiencing unexplained recurrent pregnancy loss
19. Promising prognostic markers of Preeclampsia: New avenues in waiting
20. Challenges and open issues in the management of acquired hemophilia A (AHA)
21. VKORC1 and CYP2C9 genotype distribution in Asian countries
22. Role of microparticles in recurrent miscarriages and other adverse pregnancies: a review
23. Influence of CYP2C9 and VKORC1 gene polymorphisms on warfarin dosage, over anticoagulation and other adverse outcomes in Indian population
24. A novel homozygous frameshift mutation in Exon 7 of the ADAMTS13 gene in a patient with congenital thrombotic thrombocytopenic purpura from India: a case report
25. Investigation of Plasminogen Activator Inhibitor‐1 (PAI‐1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case‐control study
26. Acquired hemophilia A: Diagnosis, aetiology, clinical spectrum and treatment options
27. Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis – A concise review
28. Synergistic effect of factor VII gene polymorphisms causing mild factor VII deficiency in a case of severe factor X deficiency
29. A novel mutation in GP1BA gene leads to mono-allelic Bernard Soulier syndrome form of macrothrombocytopenia
30. Management of pregnancy in dysfibrinogenemia cases: a dilemma
31. The Epidemiology of FVIII Inhibitors in Indian Haemophilia A Patients
32. Novel genetic abnormalities in Bernard-Soulier syndrome in India
33. Could procoagulant cell–derived microparticles have a more crucial role in pregnancy complications rather than exosomes?
34. A simple clot based assay for detection of procoagulant cell-derived microparticles
35. Possible selection of host folate pathway gene polymorphisms in patients with malaria from a malaria endemic region in North East India
36. Preeclampsia: simplified or still miles to go?
37. Re: Does low-molecular-weight heparin influence fetal growth or uterine and umbilical arterial Doppler in women with a history of early-onset uteroplacental insufficiency and an inheritable thrombophilia? Secondary randomised controlled trial results LMWH influencing fetal growth
38. COVID‐19 and preeclampsia: The unique and the mutually nonexclusive clinical manifestations.
39. Low dose emicizumab prophylaxis in haemophilia a patients: A pilot study from India.
40. Molecular pathology of haemophilia A in Indian patients: Identification of 11 novel mutations
41. Effect of anticoagulant therapy on cell-derived microparticles and pregnancy outcome in women with pregnancy loss
42. Low-Molecular-Weight Heparin for Women With Unexplained Recurrent Pregnancy Loss
43. Paradoxical Bleeding and Thrombosis in a Patient With Afibrinogenemia and Fibrinogen Mumbai Mutation
44. Phenotypic and genotypic characterization of Factor VII deficiency patients from Western India
45. Factor V Leiden gene mutation in young Indian patients with myocardial infarction
46. Hereditary protein C deficiency in Indian patients with venous thrombosis
47. A novel ELISA for diagnosis of Glanzmann’s thrombasthenia and the heterozygote carriers
48. A comprehensive screening analysis of antiphospholipid antibodies in Indian women with fetal loss
49. Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT)
50. Congenital PAI-1 deficiency results in psoas hematoma in an Indian patient
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