188 results on '"Jijina Farah"'
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2. Low-dose emicizumab prophylaxis in patients with severe hemophilia A: a retrospective study bringing new hope for our patients
3. Acquired Glanzmann thrombasthenia: a rare disorder
4. Consensus in the Management of Multiple Myeloma in India at Myeloma State of the Art 2016 Conference
5. Frequency and pattern of chromosomal abnormalities in acute myeloid leukemia from Western India: A retrospective study.
6. Safety and Efficacy of Indigenous Equine Antithymocyte Globulin Along with Cyclosporine in Subjects with Acquired Aplastic Anemia
7. Diagnosis and Management of Hemophilia Patients
8. Paroxysmal Nocturnal Hemoglobinuria
9. Cytogenetic and comparative genomic hybridization study of Indian myelodysplastic syndromes
10. Efficacy of emicizumab in von Willebrand disease (VWD) patients with and without alloantibodies to von Willebrand factor (VWF): Report of two cases and review of literature
11. A rare complication of Adult Onset Still’s Disease - A case report
12. The Prevalence of Factor V Leiden (GI69IA) and Methylenetetrahydrofolate Reductase C677T Mutations in Sickle Cell Disease in Western India
13. Hydroxyurea in sickle cell disease—A study of clinico-pharmacological efficacy in the Indian haplotype
14. Response to hydroxyurea in β thalassemia major and intermedia: Experience in western India
15. Effect of CYP2C9 and VKORC1 genetic variations on warfarin dose requirements in Indian patients
16. Hemophagocytic Lymphohistiocytosis in a 19 Year Old Critically Ill Patient
17. Hepatosplenic T Cell Lymphoma
18. Pulmonary hypertension in patients with hematological disorders following splenectomy
19. Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-(beta)-thalassaemia: a genotypic and phenotypic study
20. Pulmonary hypertension in patients with hematological disorders following splenectomy
21. An unusual presentation of pediatric acute lymphoblastic leukemia
22. The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India
23. Bone Marrow Abnormality in a case of Chronic Myeloid Leukemia
24. Acquired Glanzmann thrombasthenia: a rare disorder
25. Bone Marrow Abnormality in a case of Chronic Myeloid Leukemia
26. Exposure to Hydroxyurea During Pregnancy in Sickle-β Thalassemia: A Report of 2 Cases
27. Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-β-thalassaemia: a genotypic and phenotypic study
28. Paroxysmal nocturnal haemoglobinuria: diagnostic tests, advantages, & limitations
29. Spontaneous Resolution of Severe Aplastic Anemia following Thymic Hemorrhage
30. Anemia in Pregnancy
31. Osteoporosis in Young Haemophiliacs From Western India
32. First-trimester prenatal diagnosis in haemophilia A and B families—10 years experience from a centre in India
33. Haematuria and urolithiasis in patients with haemophilia
34. Systemic Capillary Leak Syndrome Preceding Plasma Cell Leukaemia
35. A case of atypical HUS during maintenance phase of acute lymphoblastic leukemia: A stitch in time saves nine
36. Mutation profile in Indian primary myelofibrosis patients and its clinical implications
37. FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from India
38. Comparison of in-vitro and in-vivo response to fetal hemoglobin production and a-mRNA expression by hydroxyurea in Hemoglobinopathies
39. Wiskott-Aldrich Syndrome Presenting with JMML-Like Blood Picture and Normal Sized Platelets
40. Hemophagocytic Lymphohistiocytosis in a 19 Year Old Critically Ill Patient
41. Microbial Etiology of Febrile Neutropenia
42. Ruxolitinib-associated tuberculosis - A rare complication of a novel drug!
43. Nilotinib induced skin rash in chronic myeloid leukemia patients: A case series
44. Post-splenectomy response in adult patients with immune thrombocytopenic purpura
45. Unusual Clinical Presentations of Familial Hemophagocytic Lymphohistiocytosis Type-2
46. Safety and Efficacy of Indigenous Equine Antithymocyte Globulin Along with Cyclosporine in Subjects with Acquired Aplastic Anemia
47. Myeloproliferative Hypereosinophilic Syndrome Presenting as Cardiac Failure and Response to Imatinib
48. FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from India
49. The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Mutations in Sickle Cell Disease in Western India
50. Hepatosplenic T Cell Lymphoma
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