Works by Das, Reena
Results: 144
The spread and internationalisation of South African retail chains and the implications of market power.
- Published in:
- International Review of Applied Economics, 2019, v. 33, n. 1, p. 30, doi. 10.1080/02692171.2019.1523855
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- Article
Thromboembolic complications in childhood nephrotic syndrome: a clinical profile.
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- Clinical & Experimental Nephrology, 2014, v. 18, n. 5, p. 803, doi. 10.1007/s10157-013-0917-2
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- Article
Folate and Vitamin B12 Status in Women of Reproductive Age in Rural Haryana, India: Estimating Population‐Based Prevalence for Neural Tube Defects.
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- Birth Defects Research, 2024, v. 116, n. 8, p. 1, doi. 10.1002/bdr2.2390
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- Article
Unearthing the genotype‐inhibitor phenotype association in severe haemophilia A: A north Indian cohort study.
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- Haemophilia, 2024, v. 30, n. 2, p. 410, doi. 10.1111/hae.14948
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- Article
Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect.
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- Haemophilia, 2023, v. 29, n. 2, p. 591, doi. 10.1111/hae.14730
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- Article
Clericuzio‐type poikiloderma with neutropenia in a patient from India.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 1, p. 278, doi. 10.1002/ajmg.a.61943
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- Article
First reported co‐occurrence of "GATA1‐mutated X‐linked thrombocytopenia with thalassemia (XLTT)" with heterozygous β‐thalassemia.
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- International Journal of Laboratory Hematology, 2023, v. 45, n. 6, p. 999, doi. 10.1111/ijlh.14130
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- Article
β‐thalassemia intermedia mimicking β‐thalassemia trait: The importance of family studies and HBB genotyping in phenotypically ambiguous cases.
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- 2023
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- Letter to the Editor
Cold-type autoimmune hemolytic anaemia in a patient with primary bone marrow diffuse large B-cell lymphoma.
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- 2022
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- Case Study
A rare occurrence of haemophilia A in a female due to compound heterozygosity of a de novo missense variant (presenting as pseudohomozygous) in F8 gene with Xq28 deletion inherited from mother.
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- 2022
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- Publication type:
- Case Study
Hemoglobin Andrew‐Minneapolis‐Bijnor HBB:c.[413T>C;435G>C] in a complex genotype with β‐thalassemia trait: A diagnostic and management conundrum.
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- 2022
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- Publication type:
- Letter to the Editor
Identification of peripheral blood CD26+ leukemic stem cells has a potential role in the rapid diagnosis of chronic myeloid leukemia.
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- International Journal of Laboratory Hematology, 2022, v. 44, n. 3, p. 518, doi. 10.1111/ijlh.13807
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- Publication type:
- Article
The relative expression levels of CD148 and CD180 on clonal B cells and CD148/CD180 median fluorescence intensity ratios are useful in the characterization of mature B cell lymphoid neoplasms infiltrating blood and bone marrow – Results from a single centre pilot study
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- International Journal of Laboratory Hematology, 2021, v. 43, n. 5, p. 1123, doi. 10.1111/ijlh.13467
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- Article
The utility of fluorescence in situ hybridization testing in patients clinically suspected of myelodysplastic syndrome or myelodysplastic syndrome/myeloproliferative neoplasm overlap is limited in the absence of significant morphological dysplasia.
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- International Journal of Laboratory Hematology, 2020, v. 42, n. 6, p. e287, doi. 10.1111/ijlh.13322
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- Article
IMAGES IN HAEMATOLOGY The reticulin stain in bone marrow biopsies – beyond marrow fibrosis.
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- 2003
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- Publication type:
- Other
BUDD-CHIARI SYNDROME ASSOCIATED WITH HOMOZYGOUS FACTOR V LEIDEN MUTATION.
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- British Journal of Haematology, 1999, v. 105, n. 3, p. 842, doi. 10.1046/j.1365-2141.1999.01487.x
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- Article
Familial genotypic and phenotypic heterogeneity and its implications on genetic counseling exemplified in two cases of hereditary pyropoikilocytosis/erythrocytic spectrin‐linked hemolytic anemia masquerading as congenital dyserythropoietic anemia.
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- Pediatric Blood & Cancer, 2021, v. 68, n. 10, p. 1, doi. 10.1002/pbc.29181
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- Article
HbH disease due to compound heterozygosity for hemoglobins Zürich-Albisrieden and Sallanches.
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- 2020
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- Publication type:
- Letter
Flow cytometric expression of Bcl-2, Mcl-1, and their ratios correlates with primary and secondary cytogenetic changes and their combinations in multiple myeloma.
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- Annals of Hematology, 2024, v. 103, n. 12, p. 5473, doi. 10.1007/s00277-024-06004-3
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- Publication type:
- Article
Pharmacogenetic guided versus standard warfarin dosing for routine clinical care with its pharmacoeconomic impact: a randomized controlled clinical trial.
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- Annals of Hematology, 2024, v. 103, n. 6, p. 2133, doi. 10.1007/s00277-024-05757-1
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- Publication type:
- Article
Concomitant large deletion and de novo duplication of factor VIII gene in an Indian patient with severe Hemophilia A.
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- Annals of Hematology, 2024, v. 103, n. 5, p. 1789, doi. 10.1007/s00277-024-05661-8
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- Publication type:
- Article
Hemoglobin Beth Israel [HBB:c.308A>G (p.Asn103Ser)]: an ultra-rare, low oxygen-affinity, non-methemoglobinemic hemoglobin diagnosed on targeted resequencing as cause of dominantly inherited benign cyanosis.
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- Annals of Hematology, 2022, v. 101, n. 12, p. 2799, doi. 10.1007/s00277-022-04989-3
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- Publication type:
- Article
Hemolytic erythrocytosis: an amalgamated phenotype from coinherited Chuvash polycythemia and G6PD Kerala-Kalyan with acquired transient stomatocytosis.
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- 2021
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- Publication type:
- Letter
Congenital dyserythropoietic anemia type IV with high fetal hemoglobin caused by heterozygous KLF1 p.Glu325Lys: first report in an Indian infant.
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- 2021
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- Publication type:
- Letter
A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemia.
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- Annals of Hematology, 2020, v. 99, n. 9, p. 2019, doi. 10.1007/s00277-020-04176-2
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- Publication type:
- Article
Randomized controlled trial of twice-daily versus alternate-day oral iron therapy in the treatment of iron-deficiency anemia.
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- 2020
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- Publication type:
- journal article
HbQ-India (HBA1:c.193G>C): hematological profiles and unique CE-HPLC findings of potential diagnostic utility in 65 cases.
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- 2017
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- Publication type:
- Letter
Hepatic and Cardiac Iron-load in Children on Long-term Chelation with Deferiprone for Thalassemia Major.
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- Indian Pediatrics, 2018, v. 55, n. 7, p. 573, doi. 10.1007/s13312-018-1299-z
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- Publication type:
- Article
Growth failure in hereditary spherocytosis and the effect of splenectomy.
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- Indian Pediatrics, 2017, v. 54, n. 7, p. 563, doi. 10.1007/s13312-017-1069-3
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- Publication type:
- Article
Hereditary Spherocytosis in Children: Profile and Post-splenectomy Outcome.
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- Indian Pediatrics, 2014, v. 51, n. 2, p. 139, doi. 10.1007/s13312-014-0348-5
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- Article
Isolation of a novel strain of Planomicrobium chinense from diesel contaminated soil of tropical environment.
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- Journal of Basic Microbiology, 2013, v. 53, n. 9, p. 723, doi. 10.1002/jobm.201200131
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- Publication type:
- Article
Prothrombotic gene polymorphisms and plasma factors in young north Indian survivors of acute myocardial infarction.
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- Journal of Thrombosis & Thrombolysis, 2012, v. 34, n. 2, p. 276, doi. 10.1007/s11239-012-0734-6
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- Publication type:
- Article
Thrombophilic risk factors are laterally associated with Apolipoprotein E gene polymorphisms in deep vein thrombosis patients: An Indian study.
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- Phlebology, 2019, v. 34, n. 5, p. 324, doi. 10.1177/0268355518802693
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- Publication type:
- Article
The inter-relationships between regulation and competition enforcement in the South African liquid fuels industry.
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- Journal of Energy in Southern Africa, 2015, v. 26, n. 1, p. 11, doi. 10.17159/2413-3051/2015/v26i1a2216
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- Publication type:
- Article
New approaches to supermarket supplier development programmes in Southern Africa.
- Published in:
- Development Southern Africa, 2021, v. 38, n. 1, p. 4, doi. 10.1080/0376835X.2020.1780565
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- Article
The implications for suppliers of the spread of supermarkets in southern Africa.
- Published in:
- Development Southern Africa, 2018, v. 35, n. 3, p. 334, doi. 10.1080/0376835X.2018.1452715
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- Article
The internationalisation of supermarkets and the nature of competitive rivalry in retailing in southern Africa.
- Published in:
- Development Southern Africa, 2018, v. 35, n. 3, p. 315, doi. 10.1080/0376835X.2017.1390440
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- Publication type:
- Article
Correlating clinical and laboratory diagnostic modalities in the diagnosis of epidermolysis bullosa in a resource‐poor setting.
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- Journal of Cutaneous Pathology, 2022, v. 49, n. 5, p. 454, doi. 10.1111/cup.14208
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- Publication type:
- Article
Severe hemophagocytic lymphohistiocytosis in adults-experience from an intensive care unit from North India.
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- Indian Journal of Critical Care Medicine, 2012, v. 16, n. 4, p. 198, doi. 10.4103/0972-5229.106501
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- Publication type:
- Article
ThalInd, a β-thalassemia and hemoglobinopathies database for India: defining a model country-specific and disease-centric bioinformatics resource.
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- Human Mutation, 2011, v. 32, n. 8, p. 887, doi. 10.1002/humu.21510
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- Publication type:
- Article
Role of blood and bone marrow examination in the diagnosis of mature lymphoid neoplasms in patients presenting with isolated splenomegaly.
- Published in:
- Hematology, 2015, v. 20, n. 9, p. 530, doi. 10.1179/1607845415Y.0000000005
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- Publication type:
- Article
Spectrum of diseases diagnosed on bone marrow examination of 285 infants in a single tertiary care center.
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- Hematology, 2015, v. 20, n. 3, p. 175, doi. 10.1179/1607845414Y.0000000184
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- Publication type:
- Article
Congenital dyserythropoietic anemia, type II with SEC23B exon 12 c.1385 A → G mutation, and pseudo-Gaucher cells in two siblings.
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- Hematology, 2015, v. 20, n. 2, p. 104, doi. 10.1179/1607845414Y.0000000166
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- Publication type:
- Article
Anemia in malignancies: Pathogenetic and diagnostic considerations.
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- Hematology, 2015, v. 20, n. 1, p. 18, doi. 10.1179/1607845414Y.0000000161
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- Publication type:
- Article
Spectrum of pure red cell aplasia in adult population of north-west India.
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- Hematology, 2008, v. 13, n. 2, p. 88, doi. 10.1179/102453308X315979
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- Publication type:
- Article
Investigation of persistent hypochromic microcytosis unmasks hemoglobin Evanston [α 14 (A12) Try→Arg] in a patient of cyclic thrombocytopenia preceding Takayasu's disease.
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- Hematology, 2005, v. 10, n. 5, p. 427, doi. 10.1080/10245330500214148
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- Publication type:
- Article
Serum iron indices in COVID‐19‐associated mucormycosis: A case–control study.
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- Mycoses, 2022, v. 65, n. 1, p. 120, doi. 10.1111/myc.13391
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- Publication type:
- Article
AUTOMATED RETICULOCYTE RESPONSE IS A GOOD PREDICTOR OF BONE-MARROW RECOVERY IN PEDIATRIC MALIGNANCIES.
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- Pediatric Hematology & Oncology, 2006, v. 23, n. 4, p. 299, doi. 10.1080/08880010600629502
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- Publication type:
- Article
HEMATOLOGICAL DISORDERS IN DOWN SYNDROME: Ten-Year Experience at a Tertiary Care Centre in North India.
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- Pediatric Hematology & Oncology, 2005, v. 22, n. 6, p. 507, doi. 10.1080/08880010591002350
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- Publication type:
- Article
Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait.
- Published in:
- European Journal of Haematology, 2005, v. 74, n. 4, p. 333, doi. 10.1111/j.1600-0609.2004.00390.x
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- Publication type:
- Article