47 results on '"Ghosh, K."'
Search Results
2. Second trimester prenatal diagnosis in Glanzmannʼs Thrombasthenia
3. Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families
4. Prenatal diagnosis in a haemophilia carrier with triplet pregnancy
5. Novel therapeutic approaches for haemophilia
6. Rare coagulation factor deficiencies: a countrywide screening data from India
7. Immune regulatory gene polymorphisms as predisposing risk factors for the development of factor VIII inhibitors in Indian severe haemophilia A patients
8. Polymorphic markers in VWF gene: Application in genetic diagnosis of affected families with VWD: PO-MO-254
9. Molecular pathology of severe von Willebrand disease in Indian population: PO-MO-253
10. Delayed vitamin k-deficiency related bleeding: Is it genetically linked?: PO-TU-270
11. Heterozygote frequencies of common polymorphic markers of factor VIII (f8) and factor IX (f9) genes in indigenous Nepali population
12. Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected
13. An improved, semi quantitative clot based assay for factor XIII
14. Double mutations in haemophilia: muddling strangers or indifferent partners in crime?
15. Diffuse alveolar haemorrhage with severe haemophilia
16. Molecular basis of factor X deficiency cases from India
17. A sensitive and specific chromogenic assay for the detection of “functional FVIII inhibitors”: 17P31
18. Haemophilia care in India: innovations and integrations by various chapters of Haemophilia Federation of India (HFI)
19. Antiphospholipid antibodies in haemophilia patients with severe bleeding tendency: cause, consequence or a consequential cause?
20. Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent
21. Successful surgery in severe haemophilia – a two-stage replacement therapy in resource-poor countries
22. Establishment of a new mismatch PCR-RFLP technique for detection of G10430A common mutation present in moderate to mild haemophilia B patients belonging to Gujarati community from the western part of India
23. Quality and easy availability of medical support overwhelmingly determines the attitude and belief towards genetic testing in haemophilia
24. Correlation of thromboelastographic patterns with clinical presentation and rationale for use of antifibrinolytics in severe haemophilia patients
25. Fractures of long bones in severe haemophilia
26. Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders
27. Thromboelastographic characterization of severe factor VIII and factor IX deficient patients: 20 PO 655
28. Thrombohaemorrhagic balance in haemophilia- implications for an alternative therapeutic approach: 20 PO 656
29. Intracranial haemorrhage in severe haemophilia: prevalence and outcome in a developing country
30. Anticoagulation in haemophilia patients with prosthetic valve replacement
31. Role of epsilon amino caproic acid in the management of haemophilic patients with inhibitors
32. Inherited haemostatic disorders in idiopathic menorrhagia: Do the special interest of a hemostatic laboratory make a difference?
33. ELISA for factor VIII antibodies: does it detect antibodies much before the conventional Bethesda assay?
34. First-time development of FVIII inhibitor in haemophilia patients during the postoperative period
35. Genomic interaction in haemophilia: uncharted territory
36. Danazol therapy in factor X deficiency: more questions than answers
37. Carrier detection and prenatal diagnosis in haemophilia in India: realities and challenges
38. Haemorrhage in upper cervical cord: an unusual manifestation in moderate haemophilia patients who ride motorbikes
39. Ophthalmic surgery in haemophilia
40. Development of inhibitors in patients with haemophilia from India
41. Milder clinical presentation of haemophilia A with severe deficiency of factor VIII as measured by one-stage assay
42. First trimester prenatal diagnosis of severe FXIII deficiency
43. Second trimester prenatal diagnosis in Glanzmann's Thrombasthenia
44. Novel therapeutic approaches for haemophilia
45. Use of the dual force system to correct chronic knee deformities due to severe haemophilia
46. Recurrent haemoperitoneum in a female patient with type III von Willebrand’s disease responded to administration of oral contraceptive
47. Acquired inhibitor to factor VIII: report of two unusual cases
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