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Increased Level of Factor VIII and Physiological Inhibitors of Coagulation in Patients with Sickle Cell Disease.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Chekkal M, Rahal MCA, Moulasserdoun K, Seghier F.
PMID: 28596657
Indian J Hematol Blood Transfus. 2017 Jun;33(2):235-238. doi: 10.1007/s12288-016-0701-z. Epub 2016 Jun 25.

Sickle cell disease (SCD) is a hemoglobinopathy characterized by hemolysis, oxidative stress, and vaso-occlusive crises. Thromboembolism also remains a serious complication and probably underestimated in the SCD. Our objective was to seek the existence of hemostasis abnormalities that predispose...

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Chekkal M, Rahal MCA, Moulasserdoun K, et al. Increased Level of Factor VIII and Physiological Inhibitors of Coagulation in Patients with Sickle Cell Disease. Indian J Hematol Blood Transfus. 2016;33(2):235-238doi: 10.1007/s12288-016-0701-z.
Chekkal, M., Rahal, M. C. A., Moulasserdoun, K., & Seghier, F. (2017). Increased Level of Factor VIII and Physiological Inhibitors of Coagulation in Patients with Sickle Cell Disease. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 33(2), 235-238. https://doi.org/10.1007/s12288-016-0701-z
Chekkal, Mohamed, et al. "Increased Level of Factor VIII and Physiological Inhibitors of Coagulation in Patients with Sickle Cell Disease." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 33,2 (2017): 235-238. doi: https://doi.org/10.1007/s12288-016-0701-z
Chekkal M, Rahal MCA, Moulasserdoun K, Seghier F. Increased Level of Factor VIII and Physiological Inhibitors of Coagulation in Patients with Sickle Cell Disease. Indian J Hematol Blood Transfus. 2017 Jun;33(2):235-238. doi: 10.1007/s12288-016-0701-z. Epub 2016 Jun 25. PMID: 28596657; PMCID: PMC5442051.
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Bullous Pyoderma Gangrenosum Associated with Hairy Cell Leukemia and Its Complete Response to Cladribine Therapy.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Jain A, Lad D, Prakash G, Khadwal A, Malhotra P, Bal A, Mallik N, Kumar N, Varma S.
PMID: 28596664
Indian J Hematol Blood Transfus. 2017 Jun;33(2):273-275. doi: 10.1007/s12288-016-0713-8. Epub 2016 Aug 11.

Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis seen in association with systemic disorders including hematologic malignancies. Hairy cell leukemia (HCL) however, is an unusual association of PG. We describe a 49-year old lady who presented to our hematology...

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Jain A, Lad D, Prakash G, et al. Bullous Pyoderma Gangrenosum Associated with Hairy Cell Leukemia and Its Complete Response to Cladribine Therapy. Indian J Hematol Blood Transfus. 2016;33(2):273-275doi: 10.1007/s12288-016-0713-8.
Jain, A., Lad, D., Prakash, G., Khadwal, A., Malhotra, P., Bal, A., Mallik, N., Kumar, N., & Varma, S. (2017). Bullous Pyoderma Gangrenosum Associated with Hairy Cell Leukemia and Its Complete Response to Cladribine Therapy. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 33(2), 273-275. https://doi.org/10.1007/s12288-016-0713-8
Jain, Ankur, et al. "Bullous Pyoderma Gangrenosum Associated with Hairy Cell Leukemia and Its Complete Response to Cladribine Therapy." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 33,2 (2017): 273-275. doi: https://doi.org/10.1007/s12288-016-0713-8
Jain A, Lad D, Prakash G, Khadwal A, Malhotra P, Bal A, Mallik N, Kumar N, Varma S. Bullous Pyoderma Gangrenosum Associated with Hairy Cell Leukemia and Its Complete Response to Cladribine Therapy. Indian J Hematol Blood Transfus. 2017 Jun;33(2):273-275. doi: 10.1007/s12288-016-0713-8. Epub 2016 Aug 11. PMID: 28596664; PMCID: PMC5442058.
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Horner's Syndrome in a Case of Granulocytic Sarcoma.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Jandial A, Nampoothiri RV, Malhotra P, Singh P, Sachdeva MUS, Varma S.
PMID: 28596669
Indian J Hematol Blood Transfus. 2017 Jun;33(2):285-287. doi: 10.1007/s12288-016-0742-3. Epub 2016 Nov 01.

No abstract available.

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Jandial A, Nampoothiri RV, Malhotra P, et al. Horner's Syndrome in a Case of Granulocytic Sarcoma. Indian J Hematol Blood Transfus. 2016;33(2):285-287doi: 10.1007/s12288-016-0742-3.
Jandial, A., Nampoothiri, R. V., Malhotra, P., Singh, P., Sachdeva, M. U. S., & Varma, S. (2017). Horner's Syndrome in a Case of Granulocytic Sarcoma. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 33(2), 285-287. https://doi.org/10.1007/s12288-016-0742-3
Jandial, Aditya, et al. "Horner's Syndrome in a Case of Granulocytic Sarcoma." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 33,2 (2017): 285-287. doi: https://doi.org/10.1007/s12288-016-0742-3
Jandial A, Nampoothiri RV, Malhotra P, Singh P, Sachdeva MUS, Varma S. Horner's Syndrome in a Case of Granulocytic Sarcoma. Indian J Hematol Blood Transfus. 2017 Jun;33(2):285-287. doi: 10.1007/s12288-016-0742-3. Epub 2016 Nov 01. PMID: 28596669; PMCID: PMC5442067.
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Rate of seroconversion in repeat blood donors at the national blood centre, kuala lumpur.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Nafishah A, Asiah MN, Syimah AT, Mohd Zahari TH, Yasmin A, Normi M, Anza E, Shahnaz M, Narazah MY.
PMID: 24839364
Indian J Hematol Blood Transfus. 2014 Jun;30(2):105-10. doi: 10.1007/s12288-012-0213-4. Epub 2012 Dec 21.

The World Health Organization (WHO) recommend that all donated blood are to be screened for at least three viral infections [human immunodeficiency virus (HIV), hepatitis C virus (HCV), hepatitis B virus (HBV)]. The National Blood Centre, Kuala Lumpur (NBCKL)...

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Nafishah A, Asiah MN, Syimah AT, et al. Rate of seroconversion in repeat blood donors at the national blood centre, kuala lumpur. Indian J Hematol Blood Transfus. 2012;30(2):105-10doi: 10.1007/s12288-012-0213-4.
Nafishah, A., Asiah, M. N., Syimah, A. T., Mohd Zahari, T. H., Yasmin, A., Normi, M., Anza, E., Shahnaz, M., & Narazah, M. Y. (2014). Rate of seroconversion in repeat blood donors at the national blood centre, kuala lumpur. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 30(2), 105-10. https://doi.org/10.1007/s12288-012-0213-4
Nafishah, A, et al. "Rate of seroconversion in repeat blood donors at the national blood centre, kuala lumpur." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 30,2 (2014): 105-10. doi: https://doi.org/10.1007/s12288-012-0213-4
Nafishah A, Asiah MN, Syimah AT, Mohd Zahari TH, Yasmin A, Normi M, Anza E, Shahnaz M, Narazah MY. Rate of seroconversion in repeat blood donors at the national blood centre, kuala lumpur. Indian J Hematol Blood Transfus. 2014 Jun;30(2):105-10. doi: 10.1007/s12288-012-0213-4. Epub 2012 Dec 21. PMID: 24839364; PMCID: PMC4022912.
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A randomised controlled trial to compare intravenous iron sucrose and oral iron in treatment of iron deficiency anemia in pregnancy.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Gupta A, Manaktala U, Rathore AM.
PMID: 24839366
Indian J Hematol Blood Transfus. 2014 Jun;30(2):120-5. doi: 10.1007/s12288-012-0224-1. Epub 2013 Jan 10.

The aim of this study was to compare the efficacy and safety of intravenous iron sucrose with oral iron therapy in pregnant patients with anemia. The primary outcome of the study was increase in haemoglobin on day 7, 14...

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Gupta A, Manaktala U, Rathore AM. A randomised controlled trial to compare intravenous iron sucrose and oral iron in treatment of iron deficiency anemia in pregnancy. Indian J Hematol Blood Transfus. 2013;30(2):120-5doi: 10.1007/s12288-012-0224-1.
Gupta, A., Manaktala, U., & Rathore, A. M. (2014). A randomised controlled trial to compare intravenous iron sucrose and oral iron in treatment of iron deficiency anemia in pregnancy. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 30(2), 120-5. https://doi.org/10.1007/s12288-012-0224-1
Gupta, Avantika, et al. "A randomised controlled trial to compare intravenous iron sucrose and oral iron in treatment of iron deficiency anemia in pregnancy." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 30,2 (2014): 120-5. doi: https://doi.org/10.1007/s12288-012-0224-1
Gupta A, Manaktala U, Rathore AM. A randomised controlled trial to compare intravenous iron sucrose and oral iron in treatment of iron deficiency anemia in pregnancy. Indian J Hematol Blood Transfus. 2014 Jun;30(2):120-5. doi: 10.1007/s12288-012-0224-1. Epub 2013 Jan 10. PMID: 24839366; PMCID: PMC4022911.
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Ocular manifestations in egyptian children and young adults with sickle cell disease.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

El-Ghamrawy MK, El Behairy HF, El Menshawy A, Awad SA, Ismail A, Gabal MS.
PMID: 25435727
Indian J Hematol Blood Transfus. 2014 Dec;30(4):275-80. doi: 10.1007/s12288-014-0333-0. Epub 2014 Jan 23.

In sickle cell disease (SCD), ocular lesions result from stasis and occlusion of small eye vessels by sickled erythrocytes. Vaso-occlusive disease of the retina can be responsible for nonproliferative (NPR) and proliferative retinopathy (PR). Patients are often asymptomatic until...

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El-Ghamrawy MK, El Behairy HF, El Menshawy A, et al. Ocular manifestations in egyptian children and young adults with sickle cell disease. Indian J Hematol Blood Transfus. 2014;30(4):275-80doi: 10.1007/s12288-014-0333-0.
El-Ghamrawy, M. K., El Behairy, H. F., El Menshawy, A., Awad, S. A., Ismail, A., & Gabal, M. S. (2014). Ocular manifestations in egyptian children and young adults with sickle cell disease. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 30(4), 275-80. https://doi.org/10.1007/s12288-014-0333-0
El-Ghamrawy, Mona Kamal, et al. "Ocular manifestations in egyptian children and young adults with sickle cell disease." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 30,4 (2014): 275-80. doi: https://doi.org/10.1007/s12288-014-0333-0
El-Ghamrawy MK, El Behairy HF, El Menshawy A, Awad SA, Ismail A, Gabal MS. Ocular manifestations in egyptian children and young adults with sickle cell disease. Indian J Hematol Blood Transfus. 2014 Dec;30(4):275-80. doi: 10.1007/s12288-014-0333-0. Epub 2014 Jan 23. PMID: 25435727; PMCID: PMC4243417.
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Bone mineral density in hemophilia patients.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Roushan N, Meysamie A, Managhchi M, Esmaili J, Dormohammadi T.
PMID: 25435741
Indian J Hematol Blood Transfus. 2014 Dec;30(4):351-5. doi: 10.1007/s12288-013-0318-4. Epub 2014 Jan 22.

Patients with hemophilia suffer from low bone mineral density (BMD) due to several risk factors including arthropathy and resulting immobility. Recent studies have shown variable frequency of low BMD in this group of patients. This study attempts to assess...

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Roushan N, Meysamie A, Managhchi M, et al. Bone mineral density in hemophilia patients. Indian J Hematol Blood Transfus. 2014;30(4):351-5doi: 10.1007/s12288-013-0318-4.
Roushan, N., Meysamie, A., Managhchi, M., Esmaili, J., & Dormohammadi, T. (2014). Bone mineral density in hemophilia patients. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 30(4), 351-5. https://doi.org/10.1007/s12288-013-0318-4
Roushan, Nader, et al. "Bone mineral density in hemophilia patients." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 30,4 (2014): 351-5. doi: https://doi.org/10.1007/s12288-013-0318-4
Roushan N, Meysamie A, Managhchi M, Esmaili J, Dormohammadi T. Bone mineral density in hemophilia patients. Indian J Hematol Blood Transfus. 2014 Dec;30(4):351-5. doi: 10.1007/s12288-013-0318-4. Epub 2014 Jan 22. PMID: 25435741; PMCID: PMC4243395.
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Improving Outcome of Aplastic Anaemia with HLA-Matched Sibling Donor Hematopoietic Stem Cell Transplantation: An Experience of Gujarat Cancer and Research Institute (GCRI).

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Raut SS, Shah SA, Patel KA, Shah KM, Anand AS, Talati SS, Panchal HP, Patel AA, Parikh SK, Parekh BB, Shukla SN.
PMID: 25548437
Indian J Hematol Blood Transfus. 2015 Mar;31(1):1-8. doi: 10.1007/s12288-014-0397-x. Epub 2014 May 08.

Fifteen patients, with a median age of 19 years having severe aplastic anaemia (SAA) underwent human leucocyte antigen (HLA) identical sibling donor hematopoietic stem cell transplantation (HSCT) using conditioning regimens containing cyclophosphamide with antithymocyte globulin (ATG) or a combination...

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Raut SS, Shah SA, Patel KA, et al. Improving Outcome of Aplastic Anaemia with HLA-Matched Sibling Donor Hematopoietic Stem Cell Transplantation: An Experience of Gujarat Cancer and Research Institute (GCRI). Indian J Hematol Blood Transfus. 2014;31(1):1-8doi: 10.1007/s12288-014-0397-x.
Raut, S. S., Shah, S. A., Patel, K. A., Shah, K. M., Anand, A. S., Talati, S. S., Panchal, H. P., Patel, A. A., Parikh, S. K., Parekh, B. B., & Shukla, S. N. (2015). Improving Outcome of Aplastic Anaemia with HLA-Matched Sibling Donor Hematopoietic Stem Cell Transplantation: An Experience of Gujarat Cancer and Research Institute (GCRI). Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 31(1), 1-8. https://doi.org/10.1007/s12288-014-0397-x
Raut, Shreeniwas S, et al. "Improving Outcome of Aplastic Anaemia with HLA-Matched Sibling Donor Hematopoietic Stem Cell Transplantation: An Experience of Gujarat Cancer and Research Institute (GCRI)." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 31,1 (2015): 1-8. doi: https://doi.org/10.1007/s12288-014-0397-x
Raut SS, Shah SA, Patel KA, Shah KM, Anand AS, Talati SS, Panchal HP, Patel AA, Parikh SK, Parekh BB, Shukla SN. Improving Outcome of Aplastic Anaemia with HLA-Matched Sibling Donor Hematopoietic Stem Cell Transplantation: An Experience of Gujarat Cancer and Research Institute (GCRI). Indian J Hematol Blood Transfus. 2015 Mar;31(1):1-8. doi: 10.1007/s12288-014-0397-x. Epub 2014 May 08. PMID: 25548437; PMCID: PMC4275516.
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In Vitro Susceptibility of Wistar Rat Platelets to Hydrogen Peroxide and AAPH-Induced Oxidative Stress.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Manasa K, Vani R.
PMID: 25548452
Indian J Hematol Blood Transfus. 2015 Mar;31(1):90-7. doi: 10.1007/s12288-014-0386-0. Epub 2014 Apr 11.

Hydroxyl and peroxyl radicals are biologically active species because of their likelihood to damage cellular constituents. An in vitro study on Wistar rats was conducted to investigate the influence of hydrogen peroxide (H2O2) and 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) on platelets...

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Manasa K, Vani R. In Vitro Susceptibility of Wistar Rat Platelets to Hydrogen Peroxide and AAPH-Induced Oxidative Stress. Indian J Hematol Blood Transfus. 2014;31(1):90-7doi: 10.1007/s12288-014-0386-0.
Manasa, K., & Vani, R. (2015). In Vitro Susceptibility of Wistar Rat Platelets to Hydrogen Peroxide and AAPH-Induced Oxidative Stress. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 31(1), 90-7. https://doi.org/10.1007/s12288-014-0386-0
Manasa, K, and Vani, R. "In Vitro Susceptibility of Wistar Rat Platelets to Hydrogen Peroxide and AAPH-Induced Oxidative Stress." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 31,1 (2015): 90-7. doi: https://doi.org/10.1007/s12288-014-0386-0
Manasa K, Vani R. In Vitro Susceptibility of Wistar Rat Platelets to Hydrogen Peroxide and AAPH-Induced Oxidative Stress. Indian J Hematol Blood Transfus. 2015 Mar;31(1):90-7. doi: 10.1007/s12288-014-0386-0. Epub 2014 Apr 11. PMID: 25548452; PMCID: PMC4275511.
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Hereditary spherocytosis: evaluation of 68 children.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Konca Ç, Söker M, Taş MA, Yıldırım R.
PMID: 25548458
Indian J Hematol Blood Transfus. 2015 Mar;31(1):127-32. doi: 10.1007/s12288-014-0379-z. Epub 2014 Apr 11.

To determine the clinical and hematologic features of 68 children with hereditary spherocytosis (HS). In this retrospective study, we analyzed recorded information of 68 HS patients diagnosed between March 1997 and March 2007, including clinical manifestations at admission, gender,...

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Konca Ç, Söker M, Taş MA, et al. Hereditary spherocytosis: evaluation of 68 children. Indian J Hematol Blood Transfus. 2014;31(1):127-32doi: 10.1007/s12288-014-0379-z.
Konca, �. �., Söker, M., Taş, M. A., & Yıldırım, R. (2015). Hereditary spherocytosis: evaluation of 68 children. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 31(1), 127-32. https://doi.org/10.1007/s12288-014-0379-z
Konca, Çapan, et al. "Hereditary spherocytosis: evaluation of 68 children." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 31,1 (2015): 127-32. doi: https://doi.org/10.1007/s12288-014-0379-z
Konca Ç, Söker M, Taş MA, Yıldırım R. Hereditary spherocytosis: evaluation of 68 children. Indian J Hematol Blood Transfus. 2015 Mar;31(1):127-32. doi: 10.1007/s12288-014-0379-z. Epub 2014 Apr 11. PMID: 25548458; PMCID: PMC4275513.
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Granular ALL in an Elderly Woman Diagnosed by Flow Cytometric Immunophenotyping.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Louis GB, Sharma P, Varma N, Varma S.
PMID: 25548466
Indian J Hematol Blood Transfus. 2015 Mar;31(1):156-8. doi: 10.1007/s12288-013-0258-z. Epub 2013 Apr 26.

No abstract available.

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Louis GB, Sharma P, Varma N, et al. Granular ALL in an Elderly Woman Diagnosed by Flow Cytometric Immunophenotyping. Indian J Hematol Blood Transfus. 2013;31(1):156-8doi: 10.1007/s12288-013-0258-z.
Louis, G. B., Sharma, P., Varma, N., & Varma, S. (2015). Granular ALL in an Elderly Woman Diagnosed by Flow Cytometric Immunophenotyping. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 31(1), 156-8. https://doi.org/10.1007/s12288-013-0258-z
Louis, G Balan, et al. "Granular ALL in an Elderly Woman Diagnosed by Flow Cytometric Immunophenotyping." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 31,1 (2015): 156-8. doi: https://doi.org/10.1007/s12288-013-0258-z
Louis GB, Sharma P, Varma N, Varma S. Granular ALL in an Elderly Woman Diagnosed by Flow Cytometric Immunophenotyping. Indian J Hematol Blood Transfus. 2015 Mar;31(1):156-8. doi: 10.1007/s12288-013-0258-z. Epub 2013 Apr 26. PMID: 25548466; PMCID: PMC4275539.
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Micro-organisms Associated with Febrile Neutropenia in Patients with Haematological Malignancies in a Tertiary Care Hospital in Eastern India.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Mandal PK, Maji SK, Dolai TK, De R, Dutta S, Saha S, Bhattacharyya M.
PMID: 25548444
Indian J Hematol Blood Transfus. 2015 Mar;31(1):46-50. doi: 10.1007/s12288-014-0393-1. Epub 2014 May 04.

There is paucity of information from eastern India with regard to observed dominant micro-organisms causing febrile neutropenia (FN) in patients with haematological malignancies. To identify the prevalence of pathogenic microorganisms associated with FN. A total number of 268 episodes...

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Mandal PK, Maji SK, Dolai TK, et al. Micro-organisms Associated with Febrile Neutropenia in Patients with Haematological Malignancies in a Tertiary Care Hospital in Eastern India. Indian J Hematol Blood Transfus. 2014;31(1):46-50doi: 10.1007/s12288-014-0393-1.
Mandal, P. K., Maji, S. K., Dolai, T. K., De, R., Dutta, S., Saha, S., & Bhattacharyya, M. (2015). Micro-organisms Associated with Febrile Neutropenia in Patients with Haematological Malignancies in a Tertiary Care Hospital in Eastern India. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 31(1), 46-50. https://doi.org/10.1007/s12288-014-0393-1
Mandal, Prakas Kumar, et al. "Micro-organisms Associated with Febrile Neutropenia in Patients with Haematological Malignancies in a Tertiary Care Hospital in Eastern India." Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion vol. 31,1 (2015): 46-50. doi: https://doi.org/10.1007/s12288-014-0393-1
Mandal PK, Maji SK, Dolai TK, De R, Dutta S, Saha S, Bhattacharyya M. Micro-organisms Associated with Febrile Neutropenia in Patients with Haematological Malignancies in a Tertiary Care Hospital in Eastern India. Indian J Hematol Blood Transfus. 2015 Mar;31(1):46-50. doi: 10.1007/s12288-014-0393-1. Epub 2014 May 04. PMID: 25548444; PMCID: PMC4275510.
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