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An unusual etiology of plummer-Vinson syndrome

Jain A, Agrawal P, Malhotra P, Nada R, Varma S

No abstract available.
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A weeping ulcer that vanished with a ‘SMILE’

Jain A, Prakash G, Bal A, Malhotra P, Varma S

No abstract available.
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A young man with acute respiratory distress syndrome: eosinophilia is not always “benign”

Jain A, Malhotra P, Suri V, Agarwal R, Bal A, Varma S

No abstract available.
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Synchronous hairy cell leukemia and chronic lymphocytic leukemia: a case report with a brief review of literature

Rastogi P, Jeyaraman , Sachdeva M, Malhotra P, Ahluwalia

No abstract available.
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Granulocytic dysplasia: an indicator of clonal evolution in patients with chronic myeloid leukemia

Rajpal S, Nampoothiri RV, Sreedharanunni S, Parihar M, Malhotra P, Varma N

No abstract available.
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Late Onset Agranulocytosis with Clozapine Associated with HLA DR4 Responding to Treatment with Granulocyte Colony-stimulating Factor: A Case Report and Review of Literature

Singh A, Grover S, Malhotra P, Varma SC

Agranulocytosis as a side effect of clozapine has been reported to be associated with initial phases of treatment, i.e., first six months. Agranulocytosis with clozapine during the initial phases of...
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Impact of ABO blood group antigens on residual factor VIII levels and risk of inhibitor development in hemophilia A

Ray D, Kumar N, Hans C, Kler A, Jain R, Bansal D, Trehan A, Jain A, Malhotra P, Ahluwalia J

Background The clinical phenotype of hemophilia A (HA) does not always correlate with severity. Similarly, the presence of inhibitors does not necessarily increase the risk of bleeding. This paradox between clinical and laboratory...
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A comparative study between light transmission aggregometry and flow cytometric platelet aggregation test for the identification of platelet function defects in patients with bleeding

Sharma P, Sachdeva MUS, Kumar N, Bose S, Bose P, Uppal V, Malhotra P, Bansal D, Varma N, Ahluwalia J

Background Platelet aggregation studies using conventional light transmission aggregometry (LTA) have several disadvantages and require strict pre-analytical measures for reliable results. We aimed to examine the utility of flow cytometric platelet aggregation...
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Genomic alterations in chronic lymphocytic leukemia and their correlation with clinico-hematological parameters and disease progression

Srinivasan VK, Naseem S, Varma N, Lad DP, Malhotra P

Background Chronic lymphocytic leukemia (CLL) is a heterogeneous disease, which is attributed to differences in the genetic characteristics of the leukemic clone. We studied the genomic profile of 52 treatment-naïve CLL...
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Bendamustine in combination with ifosfamide, etoposide, and vinorelbine (VIBE) is an effective salvage regimen for heavily pre-treated patients with relapsed or refractory Hodgkin lymphoma: a single-center experience

Prakash G, Jain A, Sahu K, Bal A, Singh C, Basher R, Singh H, Mishra K, Jandial A, Lad D, Khadwal A, Srinivasan R, Das A, Varma N, Varma S, Malhotra P

Background: This study evaluated the outcomes of patients with refractory/relapsed Hodgkin lymphoma (RRHL) treated with a bendamustine-based regimen in combination with ifosfamide, etoposide, and vinorelbine (VIBE). Methods: Consecutive RRHL patients who...
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Plasma cell leukemia in North India: retrospective analysis of a distinct clinicohematological entity from a tertiary care center and review of literature

Bommannan , Sachdeva M, Malhotra P, Kumar N, Sharma P, Naseem S, Ahluwalia , Das R, Varma N, Prakash G, Khadwal A, Srinivasan R, Varma S

BACKGROUND: Plasma cell leukemia (PCL) is a rare and aggressive plasma cell neoplasm. In PCL, clonal plasma cells comprise ≥20% of the peripheral blood (PB) leukocytes and/or the absolute clonal...
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