ABSTRACT ID | TITLE | PRESENTER NAME |
---|---|---|
BHC-601 | SEROPREVALENCE OF VIRAL TRANSFUSION TRANSMITTED INFECTIONS (HIV, HBV AND HCV) AND THEIR POSSIBLE CORRELATION WITH ABO AND RHD BLOOD GROUP TYPES IN BLOOD DONORS AT A TERTIARY CARE INSTITUTE IN HARYANA | PAWAN SINGH |
BHC-602 | CLINICALLY SIGNIFICANT ANTI-M ANTIBODY IN AN M-POSITIVE INDIVIDUAL: A CASE REPORT WITH IMPLICATIONS FOR BLOOD TRANSFUSION MANAGEMENT | SUSHREE DASH |
BHC-603 | AN UNSUAL PRESENTATION OF EXTRAMEDULLARY HEMATOPOIESIS IN A ADULT | MANASWINEE MALLIK |
BHC-604 | BACTERIAL PATHOGENS CAUSING BLOODSTREAM INFECTION IN CANCER PATIENTS: ORGANISM PROFILE AND SUSCEPTIBILITY PATTERNS. | HEMALI KADU |
BHC-605 | ACUTE FEBRILE ILLNESS IN MALNUTRITION - COCKTAIL FOR FATAL PATHOLOGY | HITAKSHI GOEL |
BHC-606 | THE ENIGMA OF BIG SPLEEN DISEASE IN A CHILD-AN APPROACH TO CLINICAL DIAGNOSIS | LAKSHINDER KAUR |
BHC-607 | WHY AM I GREY? | ABHIJITH LAKSHMAN |
BHC-608 | UNUSUAL CASE OF SEVERE HEMOLYTIC ANEMIA | DIVYA T |
BHC-609 | COMPARISON OF H-SCORE VS. 2004 CRITERIA FOR DIAGNOSIS OF HLH | KOMAL KELA |
BHC-610 | HISTOPLASMOSIS IN AN IMMUNOCOMPETENT PATIENT: AN UNUSUAL PRESENTATION | SUGANDHA SUMMAN |
BHC-611 | MOYAMOYA SYNDROME IN A SICKLE CELL DISEASE | INDRANI MONDAL |
BHC-612 | A RARE SITE OF THROMBOSIS IN APLASTIC ANEMIA WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA | MANASWINEE MALLIK |
BHC-613 | UTILITY OF MENTZER’S INDEX IN IDENTIFYING THALASSEMIA TRAIT IN RESOURCE POOR SETTINGS | DIVYA DONEPUDI |
BHC-614 | A RARE BLEEDING DISORDER - : PROTHROMBIN DEFICIENCY | BANUKEERTHANA RAJASEKARAN |
BHC-615 | BONE MARROW EXAMINATION IN THE DIAGNOSIS OF INFECTIOUS PATHOLOGY: AN OFTEN UNDERUTILIZED DIAGNOSTIC TOOL | MONIKA MAHARJAN |
BHC-616 | AN UNUSUAL CASE OF CYTOMEGALOVIRUS (CMV) INDUCED NEUTROPENIA IN A 10 MONTH OLD MALE CHILD. | SAURABH SINGH |
BHC-617 | SECONDARY HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN A BRUCELLOSIS PATIENT - A RARE CASE REPORT | SONALIKA PRIYADARSHINI SAHOO |
BHC-618 | THE FROZEN CASTLE | PRIYATHERSINI NAGARAJAN |
BHC-619 | HEMOSTATIC MANAGEMENT IN A CASE OF GLANZMANN’S THROMBASTHENIA WITH REFRACTORY GI BLEED | CHAITANYA H BALAKRISHNAN |
BHC-620 | TRANSIENT ABNORMAL MYELOPOIESIS IN A DOWN’S SYNDROME BABY - A CASE REPORT | SAPNA PATEL MC |
BHC-621 | GETTING EVEN WITH EVAN'S | SUSHMA B |
BHC-622 | PARVOVIRAL INFECTION OF BONE MARROW MASQUERADING AS LYMPHOMA IN AN ANTI-PHOSPHOLIPID ANTIBODY (APLA) POSITIVE YOUNG MALE – A CASE REPORT | SHEELA DEVI CS |
BHC-623 | BILATERAL ADRENAL HAEMORRHAGE IN A CASE OF ANTIPHOSPHOLIPID ANTIBODY SYNDROME – AN UNUSUAL PRESENTATION | VERONICA LOBO |
BHC-624 | AGGRESSIVE HLH – A HAVOC IN DISSEMINATED TUBERCULOSIS | SOUMYA KANTI MANDAL |
BHC-625 | A STUDY OF ANTIPROTHROMBIN / ANTIPHOSPHATIDYL SERINE ANTIBODIES IN PATIENTS OF PEDIATRIC SYSTEMIC LUPUS ERYTHEMATOSUS. | SANJOLI CHUGH |
BHC-626 | HEMATOPATHOLOGICAL INSIGHTS INTO PITUITARY APOPLEXY SECONDARY TO PITUITARY ADENOMA | GUTTIKONDA SATHVIK |
BHC-627 | BONE MARROW AMYLOIDOSIS (AMYLOID LIGHT CHAIN) PRESENTING AS MASSIVE SPLENOMEGALY IN THE ELDERLY. AN INTERESTING CASE REPORT. | APARNA SINGH |
BHC-628 | PREVALENCE AND SPECTRUM OF HEMOGLOBINOPATHIES IN A TERTIARY CARE CENTRE OF UTTARAKHAND | DIVYA KUMARI |
BHC-629 | ALL TMA IS NOT TTP, AMONGST OTHERS, CONSIDER MALIGANANCY! | PANKHI DUTTA |
BHC-630 | AN UNUSUAL PRESENTATION OF DISSEMINATED TUBERCULOSIS ASSOCIATED WITH FLORID HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (HLH) SYNDROME | KRITIKA DEWAN |
BHC-631 | DKMS BMST PATIENT FUNDING PROGRAM: GIVING HOPE FOR A HEALTHY FUTURE | RESHMA KUMARI MV |
BHC-632 | MOLECULAR SPECTRUM OF INHERITED PLATELET DISORDERS | RAJKUMAR VENKASTESAN |
BHC-633 | GENOMIC EVALUATION OF YOUNG PATIENTS WITH MYOCARDIAL INFARCTION | BIPIN KULKARNI |
BHC-634 | SHADES OF HEMOLYSIS: AN UNUSUAL ENCOUNTER BETWEEN TRAITS AND ANTIBODIES | SUMBUL MAZAHAR |
BHC-635 | A RARE OCCURRENCE OF HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN A SICKLE CELL DISEASE PATIENT LEADING TO UNFAVOURABLE NEUROSEQUELAE | ARINDAM MANDAL |
BHC-636 | GSTA1 DIPLOTYPES INFLUENCE INTRAVENOUS BUSULFAN PHARMACOKINETICS IN CHILDREN WITH BETA-THALASSEMIA MAJOR UNDERGOING MATCHED ALLOGENEIC HAEMATOPOIETIC STEM CELL TRANSPLANTATION | AGILA JAYARAMAN |
BHC-637 | A MODEL-INFORMED PRECISION OF ONCE-DAILY BUSULFAN DOSING IN PATIENTS UNDERGOING ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANTATION | RAJESH NAGARAJAN |
BHC-638 | ROLE OF TRANSMEMBRANE SERINE PROTEASE 6 GENE VARIANTS ON PATHOPHYSIOLOGY OF IRON DEFICIENCY ANEMIA | SANJAY PANDEY |
BHC-639 | CASE REPORT OF NIEMANN-PICK DISEASE TYPE A (NPD-A) | MARY PUSHPA MURMU MURMU |
BHC-640 | DIAGNOSTIC OUTCOME OF BONE MARROW EXAMINATION IN VARIOUS HEMATOLOGICAL DISORDER: AN EXPERIENCE FROM TERTIARY CARE HOSPITALI | VINITA PASWAN |
BHC-641 | EVALUATION OF RISK FACTORS COMPLICATING NONTRANSFUSION DEPENDENT THALASSEMIA. | ANIL KUMAR DASH |
BHC-642 | PREVALENCE OF BETA THALASSEMIA TRAIT ATTENDING ANTENATAL CHECKUP IN A TERTIARY REFERRAL HOSPITAL | ROMANCHIT UPADHYAYA |
BHC-643 | A COMPARATIVE COST ANALYSIS ASSESSING THE BURDEN OF COVID-19 ON PATIENTS UNDERGOING HEMATOPOIETIC STEM CELL TRANSPLANTATION AT A TERTIARY CARE CANCER CENTER IN EASTERN INDIA | MANIK GHOSH |
BHC-644 | SICKLE CELL DISEASE WITH SYSTEMIC LUPUS ERYTHEMATOSUS -A RARE CASE REPORT FROM WESTERN ODISHA . | BALKISHAN AGRAWALA |
BHC-645 | A CASE REPORT: VISCERAL LEISHMANIASIS (KALA-AZAR) | HELEN TUDU |
BHC-646 | LAPAROSCOPIC SPLENECTOMY IN BETA THALASSEMIA MAJOR PATIENTS: PROS AND CONS - A SINGLE CENTRE STUDY | SANIDHYA KUMAR MISHRA |
BHC-647 | THE AUTOIMMUNE HEPARIN?INDUCED THROMBOCYTOPENIA- FIRST CONFIRMED CASE IN INDIA | PALLAVI PRAKHAR |
BHC-648 | RARE CASE OF COMPOUND HETEROZYGOUS FOR HEREDITARY PERSISTENCE OF FOETAL HEMOGLOBIN AND BETA THALASSEMIA MIMICKING THALASSEMIA INTERMEDIA. | JAYITA DAS |
BHC-649 | ISOLATED MARROW TUBERCULOSIS - A HIDDEN CAUSE OF CYTOPENIAS. | MADHUSMITA MANGARAJ |
BHC-650 | A USABILITY STUDY ASSESSING HANDLING AND PREFERENCE OF THE CONCIZUMAB PEN-INJECTOR IN PATIENTS WITH HAEMOPHILIA AND CAREGIVERS | RANJAN KM |
BHC-651 | DYNAMICS OF STEM CELLS IN PERIPHERAL BLOOD (PB) DURING STEM CELL MOBILIZATIONS FOR STEM CELL TRANSPLANTATIONS, A SINGLE INSTITUTIONAL EXPERIENCE | DEBI PRASAD JENA |
BHC-653 | LEISHMANIASIS IN A KNOWN CASE OF SICKLE CELL TRAIT WITH SECONDARY HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS – A RARE CASE REPORT | MUKESH KUMAR PRADHAN |
BHC-654 | A CASE REPORT ON NUMB CHIN SYNDROME IN SICKLE CELL DISEASE | PRATYUSH KUMAR PANDA |
BHC-655 | MANAGING INTRACRANIAL HAEMORRHAGE IN PATIENTS WITH HAEMOPHILIA: AN EXPERIENCE FROM A TERTIARY CARE CENTRE | HARSHIT KHURANA |
BHC-656 | A RARE CASE OF ACUTE SOFT SKULL SYNDROME IN SICKLE CELL DISEASE PATIENT | SUCHISMITA MISRA |
BHC-657 | CLINICAL PROFILE, TREATMENT PATTERNS AND QUALITY OF LIFE IN CANCER PATIENTS WITH VENOUS THROMBOEMBOLISM | PRASHUN UPADHAYA |
BHC-658 | RARE PRESENTATION OF EXTENSIVE ERYTHEMATOUS MACULOPAPULAR SKIN LESIONS POST CLADRIBINE THERAPY IN HAIRY CELL LEUKEMIA (HCL). | NEHA MOTWANI |
BHC-659 | CLINICAL PROFILE, TREATMENT PRACTICES AND RESPONSE IN PAROXYSMAL NOCTURNAL HEMOGLOBINURIA CASES | GOUTHAM KRISHNA |
BHC-660 | RESPONSE OF RITUXIMAB IN STEROID RESISTANT IMMUNE THROMBOCYTOPENIC PURPURA - A RETROSPECTIVE STUDY | LIPSA NAYAK |
BHC-661 | CEREBRAL VENOUS SINUS THROMBOSIS IN IMMUNE THROMBOCYTOPENIA PATIENTS TREATED WITH THROMBOPOIETIN RECEPTOR AGONIST: A CASE REPORT | ADITYA DEBUKA |
BHC-662 | PRIMARY DIAGNOSIS OF LUPUS ERYTHEMATOSUS IN BONE MARROW | GIFTA CATHARINE |
BHC-663 | ADULT-ONSET EVANS SYNDROME | SHANTILATA SINGH |
BHC-664 | A RARE CASE OF SECONDARY IMMUNE MEDIATED THROMBOCYTOPENIA IN H.PYLORI POSITIVE PATIENT | MANOJ KUMAR MALIK |
BHC-665 | A RARE ENCOUNTER: UNRAVELING A CASE OF THROMBOTIC THROMBOCYTOPENIC PURPURA | SREENATH S |
BHC-666 | THREE CASES OF HYPEREOSINOPHILIC SYNDROME WITH CLONAL T CELLS AND DIFFERENT CLINICAL COURSES: A DIAGNOSTIC CONUNDRUM | AISHWARYA KARTHIKEYAN |
BHC-667 | SPECTRUM OF HAEMOGLOBIN F (FETAL) AND HAEMOGLOBIN S (SICKLE) LEVEL IN SICKLE CELL HOMOZYGOUS PATIENTS (ARAB INDIAN HAPLOTYPE) ;IN SINGLE INSTITUTION EXPERIENCES | RASHMI RANJAN BHOI |
BHC-668 | CHARACTERIZATION OF 40 NOVEL HLA CLASS I AND CLASS II ALLELES IDENTIFIED IN UMBILICAL CORD BLOOD (UCB) UNITS | SUREKA RAJENDRAN |
BHC-669 | INFECTIONS IN BONE MARROW- AN INSTITUTIONAL STUDY | MONALISHA NAYAK |
BHC-670 | PREVALENCE OF ACUTE TRANSFUSION ASSOCIATED COMPLICATIONS IN CHILDREN WITH ?-THALASSEMIA MAJOR IN A TERTIARY CARE CENTER IN NORTH INDIA: A PROSPECTIVE STUDY | ALKA YADAV |
BHC-671 | STUDY OF INHIBITOR IN PWH- A RECEIVING F-VIII CONCENTRATION (PLASMA DERIVED) | RENUKA SAHOO |
BHC-672 | AN UNUSUAL CASE OF GENERALISED LYMPHADENOPATHY WITH PURPURA | IRSHAD ALI K M |
BHC-673 | UNUSUAL CASE PRESENTATION OF GAUCHER DISEASE IN AN ADULT | METAANKSHA AHUJA |
BHC-674 | ISOLATED OSTEOSCLEROSIS VS LATE INACTIVE PAGET’S DISEASE- A DIAGNOSTIC DILEMMA. | TANYA AGGARWAL |
BHL-801 | HBA2 LEVELS IN IRON DEFICIENCY - CAN IRON DEFICIENCY MASK THALASSEMIA SCREENING ? | PREETI TRIPATHI |
BHL-802 | ASSESSMENT OF BLAST FLAG IN ADVIA 2120I CELL COUNTER BY PERIPHERAL BLOOD SMEAR EXAMINATION | BABU PILLAI |
BHL-803 | MOLECULAR WORKUP IS ESSENTIAL IN BORDERLINE HAEMOGLOBIN A? | ANJUMAN ASHOK |
BHL-804 | COMPARISON BETWEEN ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA) AND CHEMILUMINESCENCE IMMUNOASSAY (CLIA) FOR THE DETECTION OF TRANSFUSION TRANSMITTED DISEASE (TTD) MARKERS IN BLOOD DONORS | MAYANK KUMAR |
BHL-805 | ASSESSMENT OF PERIPHERAL BLOOD SMEARS THAT WERE AUTOMATICALLY STAINED BY STAINZ PLUS TO THOSE THAT WERE MANUALLY STAINED IN A TERTIARY CARE FACILITY | SWATI VAYKAR |
BHL-806 | APPLYING SIX SIGMA APPROACH TO MONITOR PERFORMANCE OF INTERNAL QUALITY CONTROL IN HEMATOLOGY LABORATORY OF A TERTIARY CARE CENTER – LESSONS LEARNT. | SHIVALI SEHGAL |
BHL-807 | DIAGNOSTIC ACCURACY OF AUTOMATED FRAGMENTED RED CELL (FRC) COUNTING IN HEMOLYTIC ANEMIA-DO POIKILOCYTES AND MICROCYTES INTERFERE? | RAJALAKSHMI RAJASHEKAR |
BHL-808 | APLASTIC ANAEMIA AS A RARE PRESENTATION IN HYPER-IGE SYNDROME (JOB SYNDROME) | SWATI SHARMA |
BHL-809 | FLAER AS A STANDALONE DIAGNOSTIC REAGENT IN PAROXYSMAL NOCTURNAL HEMOGLOBINURIA TESTING: A CALL FOR GUIDELINE REASSESSMENT AND PRACTICE EVOLUTION | PARVEEN BOSE |
BHL-810 | REFRIGERATION OF EDTA SAMPLES BETWEEN 0 TO 4 HOURS SHOWS THAT SAMPLES STAY VIABLE UPTO 24 HOURS FOR CBC ANALYSIS | PRIYANK DOODANI |
BHL-811 | RENAL OSTEODYSTROPHY-BONE MARROW BIOPSY: A CASE REPORT | ADITYA NARAYAN MONDAL |
BHL-812 | TO STUDY THE SPECTRUM OF RED CELL INDICES IN BETA THALASSEMIA ( TRAIT) | PADMALOCHAN DWIBEDY |
BHL-813 | DIAGNOSTIC UTILITY OF PLATELET PARAMETERS FOR SCREENING OF DYSLIPIDEMIC PATIENTS | SAYANTANI GHOSH HAZRA |
MH-961 | ASSESSING THE INFLUENCE OF FACTOR XIII VAL34LEU POLYMORPHISM IN INDIAN MYOCARDIALINFARCTION PATIENTS | RAVI RANJAN |
MH-962 | UNLOCKING VEXAS SYNDROME IN INDIA: DECIPHERING CLINICAL AND LABORATORY PROFILES THROUGH A MULTIFACETED CASE SERIES | AADYA KERKAR |
MH-963 | DUAL EFFECT OF HYDRALAZINE AS DEMETHYLATING AGENT OF CLOCK GENES AND DIFFERENTIAL REGULATOR OF ACUTE MYELOID LEUKAEMIA ASSOCIATED GENES. | MINAKSHI SEN |
MH-964 | MODULATING EFFECT OF BCL11A (RS11886868) GENE VARIANT ON THE PHENOTYPE OF SICKLE CELL ANAEMIA PATIENTS: A TERTIARY CARE EXPERIENCE | HARERAM PANDEY |
MH-965 | EXPLORING IGHV MUTATION STATUS AND STEREOTYPED SUBSETS IN CHRONIC LYMPHOCYTIC LEUKAEMIA (CLL): A COMPARATIVE STUDY USING SANGER SEQUENCING VERSUS CAPTURE BASED NEXT GENERATION SEQUENCING (NGS) | SHRUTI CHAUDHARY |
MH-966 | A MULTIFACETED APPROACH TO ICF SYNDROME: INVESTIGATING KARYOTYPE, IMMUNOPHENOTYPING, AND MOLECULAR FINDINGS | MANOJ V T |
MH-967 | SPECTRUM OF RARE GENETIC CAUSES OF INHERITED CYANOSIS: A CASE SERIES FROM A TERTIARY-CARE CENTRE | AISHWARYA KARTHIKEYAN |
MH-968 | MUTATIONAL SPECTRUM OF NON-DELETIONAL ALPHA THALASSAEMIA IN TERTIARY CARE SETTING | NEELAGANDAN KAMALANATHAN |
MH-969 | GENE DOSAGE QUANTITATIVE MULTIPLEX FLUORESCENT PCR AS A SCREENING TOOL FOR DETECTION OF DELETION IN DELTA-BETA THALASSEMIA | SENTHIL KUMAR GOVINDA SWAMY |
MH-970 | PEDIATRIC AML WITH CONCOMITANT DDX41 & NPM1 MUTATION: AN EXTREMELY RARE ASSOCIATION | PRATEEK DAS |
MH-971 | MYELOID NEOPLASMS WITH GERMLINE GATA2 MUTATION: A DIAGNOSTIC CONUNDRUM. | PRATEEK DAS |
MH-972 | UNRAVELING IBRUTINIB RESISTANCE IN CHRONIC LYMPHOCYTIC LEUKEMIA: A CASE STUDY ON THE ROLE OF BRUTON TYROSINE KINASE MUTATION | DEBAJANI NATHI |
MH-973 | A CASE OF CONGENITAL ERYTHROCYTOSIS CAUSED BY A NOVEL EGLN1 VARIANT – FIRST REPORT OF ECYT3 FROM INDIA | KAJOL |
MH-974 | CYSTATIN F A POTENTIAL DIAGNOSTIC BIOMARKER IN ACUTE PROMYELOCYTIC LEUKEMIA | HAMENTH KUMAR PALANI |
MH-975 | PREVALENCE OF JAK2V617F MUTATION, ITS ALLELE BURDEN IN HEPATIC VENOUS OUTFLOW TRACT OBSTRUCTION AND EXTRAHEPATIC PORTAL VENOUS OBSTRUCTION PATIENTS. A TERTIARY CARE CENTRE STUDY. | SUMAN LATA |
MH-976 | NANO VARIANT OF BCR-ABL TRANSCRIPT PRESENTING WITH ATYPICAL FEATURES: A REPORT OF TWO CASES. | PRATEEK DAS |
MH-977 | A RARE THREE-WAY COMPLEX TRANSLOCATION WITH VARIANT PHILADELPHIA CHROMOSOME T(4;9:22)(P16;Q34;Q11.2) IN A CHRONIC MYELOID LEUKEMIA PATIENT | BIBHAS KAR |
BHC-675 | INTERESTING CASE OF SLE WITH REFRACTORY HYPOPLASTIC ANEMIA | VINAYA GOPALASWAMY |