Search Results - "Pati, Hara P"

Unusual Presentation of Hairy Cell Leukemia: A Case Series of Four Clinically Unsuspected Cases by Venkatesan, S., Purohit, Abhishek, Aggarwal, Mukul, Manivannan, Prabhu, Tyagi, Seema, Mahapatra, Manoranjan, Pati, Hara P., Saxena, Renu

“…Hairy cell leukemia (HCL) is characterized by pancytopenia and usually associated with massive splenomegaly, however the same may not be true in the clinical…”
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Atypical immunophenotype of T-cell Acute Lymphoblastic Leukemia by Purohit, Abhishek, Aggarwal, Mukul, Pati, Hara P, Saxena, Renu

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Calreticulin Mutation by Immunohistochemistry: Can It Replace PCR? by Gupta, Aastha, Sazawal, Sudha, Mahapatra, Manoranjan, Pati, Hara P., Saxena, Renu

“…Before 2013, the diagnosis of about 30% to 45% cases of primary myelofibrosis (PMF) and essential thrombocythemia (ET) posed a diagnostic difficulty because of…”
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Comparison of CRP and procalcitonin for etiological diagnosis of fever during febrile neutropenia in hematology patients- an experience from a tertiary care center in Northern India by Halder, Rohan, Seth, Tulika, Chaturvedi, Pradeep K., Mishra, Priyanka, Mahapatra, Manoranjan, Pati, Hara P., Tyagi, Seema, Saxena, Renu

“…Febrile neutropenia is a common cause in morbidity and mortality during treatment of hematological neoplasms. Subjects included all cases admitted under…”
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Unusual massive bone marrow fibrosis in acute promyelocytic leukemia following arsenic trioxide therapy by Venkatesan, S, Purohit, Abhishek, Ahuja, Ankur, Chandra, Dinesh, Aggarwal, Mukul, Amrita, R, Kumar, Ravi, Mahapatra, Manoranjan, Pati, Hara P, Tyagi, Seema

“…Abstract Bone marrow fibrosis has been associated with different types of non-neoplastic conditions like granulomatous and autoimmune diseases and a variety of…”
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A Case of Iron Deficiency Anemia with Co-existing Hb Fontainebleau by Purohit, Abhishek, Aggarwal, Mukul, Colah, Roshan B, Nadkarni, Anita H, Pati, Hara P

“…Hb Fontainebleau is a rare alpha chain variant in the Indian population which generates an unknown peak on hemoglobin HPLC study and does cause diagnostic…”
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Outcomes of paroxysmal nocturnal hemoglobinuria in the pediatric age group in a resource‐constrained setting by Halder, Rohan, Mishra, Priyanka, Aggarwal, Mukul, Mannivanan, Prabhu, Dhawan, Rishi, Seth, Tulika, Tyagi, Seema, Mahapatra, Manoranjan, Pati, Hara P., Saxena, Renu

“…Paroxysmal nocturnal hemoglobinuria (PNH) is a rare acquired clonal stem cell disorder. Eculizumab and bone marrow transplantation are disease‐modifying…”
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Turnaround Time (TAT): Difference in Concept for Laboratory and Clinician by Pati, Hara P., Singh, Gurmeet

“…Lab investigations are essential in patient management and qualities of the tests reports are emphasized. But there is another aspect of quality which is often…”
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Transfusion-induced hemoglobinopathy in patients of beta-thalassemia major by Gupta, Sanjeev K, Sharma, Monica, Tyagi, Seema, Pati, Hara P

“…Apparent hemoglobinopathy acquired after blood transfusion is an uncommon cause of diagnostic dilemma resulting in repeated testing and delay in the diagnosis…”
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Proportion of CD34+CD38−CD123+ Leukemia Stem Cells at Diagnosis Varies in ELN Risk Groups and an Emerging Novel Marker for Prognosticating the Intermediate Risk patients of Acute Myeloid Leukemia: A Prospective Study by Mishra, Priyanka, Tyagi, Seema, Sharma, Rahul, Halder, Rohan, Pati, Hara P., Saxena, Renu, Mahapatra, Manoranjan

“…s The proportion of CD34  +  CD38  −  CD123  +  leukemia stem cells (LSCs) at diagnosis of Acute Myeloid Leukemia (AML) correlated with induction remission…”
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CD157 Can Replace CD24 and CD14 in a Single-Tube Flow-Cytometric Assay to Detect Paroxysmal Nocturnal Hemoglobinuria (PNH) Clones on Both Neutrophils and Monocytes: A Prospective Study From North India by Deka, Roopam, Pati, Hara P, Chandra, Dinesh, Manivannan, Prabhu, Chauhan, Richa, Tyagi, Seema, Saxena, Renu

“…Introduction As per current guidelines, detection of paroxysmal nocturnal hematuria (PNH) clones on leucocytes requires the demonstration of the loss of at…”
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Concomitant Existence of Paroxysmal Nocturnal Hemoglobinuria in a Patient with Hb E ( HBB : c.79G>A) Trait by Halder, Rohan, Sundaram, Uday Kumar D, Veetil, Karthika K, Rath, Ashish, Seth, Tulika, Tyagi, Seema, Pati, Hara P

“…Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal disorder that manifests with bone marrow failure, thrombosis and hemolysis. We present a…”
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Re-evaluation of Need for Bone Marrow Examination in Patients with Isolated Thrombocytopenia Contributors by Purohit, Abhishek, Aggarwal, Mukul, Singh, Pawan Kumar, Mahapatra, Manoranjan, Seth, Tulika, Tyagi, Seema, Saxena, Renu, Pati, Hara P., Mishra, Pravas

“…Diagnosis of immune thrombocytopenia (ITP) is based on clinical suspicion and normal peripheral smear except for thrombocytopenia. Bone marrow examination is…”
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Priapism Associated with Homozygous Hb E State: A Causal Association or an Incidental Finding? by Venkatesan, S., Purohit, Abhishek, Aggarwal, Mukul, Singh, Pawan Kr, Seth, Tulika, Pati, Hara P.

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Hairy cell leukemia: A decade long experience of North Indian Hematology Center by Somasundaram, Venkatesan, Purohit, Abhishek, Aggarwal, Mukul, Manivannan, Prabhu, Mishra, Pravas, Seth, Tulika, Tyagi, Seema, Mahapatra, Manoranjan, Pati, Hara P, Saxena, Renu

“…Hairy cell leukemia is a rare chronic B-cell disorder that follows an indolent but progressive course. This disorder is characterized by pancytopenia,…”
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Erratum to: Re-evaluation of Need for Bone Marrow Examination in Patients with Isolated Thrombocytopenia by Purohit, Abhishek, Aggarwal, Mukul, Singh, Pawan Kumar, Mahapatra, Manoranjan, Seth, Tulika, Tyagi, Seema, Saxena, Renu, Pati, Hara P., Mishra, Pravas

“…[This corrects the article DOI: 10.1007/s12288-015-0533-2.]…”
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Immunophenotypic Aberrancy of a Case of Hairy Cell Leukemia by Purohit, Abhishek, Venkatesan, S., Aggarwal, Mukul, Singh, Jasdeep, Sharma, Rahul, Mahapatra, Manoranjan, Pati, Hara P., Saxena, Renu

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Clinico-hematological profile of hereditary spherocytosis: experience from a tertiary care center in North India by Kar, Rakhee, Rao, Seema, Srinivas, Upendra M, Mishra, Pravas, Pati, Hara P

“…Hereditary spherocytosis (HS) is an inherited membranopathy characterized by phenotypic and genotypic heterogeneity. This study describes the…”
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Hereditary Spherocytosis with High Fetal Hemoglobin: An Interesting Case by Kar, Rakhee, Saxena, Renu, Pati, Hara P.

“…Raised Hb F is occasionally found in stress erythropoiesis associated with hemolytic anemias. In hereditary spherocytosis (HS), elevation of Hb F by 2-5% may…”
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Autoimmune hemolytic anemia and erythroid hypoplasia associated with hepatitis E by Mishra, Pravas, Mahapatra, Manoranjan, Kumar, Rajat, Pati, Hara P

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