Detalhe da pesquisa
1.
Multi-criteria decision making to validate performance of RBC-based formulae to screen [Formula: see text]-thalassemia trait in heterogeneous haemoglobinopathies.
BMC Med Inform Decis Mak
; 24(1): 5, 2024 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38167309
2.
Hematological and genetic profiles of persons with co-inherited heterozygous ß-thalassemia and supernumerary α-globin genes.
Eur J Haematol
; 110(5): 510-517, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36598439
3.
Prognostic significance of extramedullary disease (EMD) detected on pre-transplant 18F-FDG PET/CT in patients with multiple myeloma: Results of PIPET-M trial.
Med J Armed Forces India
; 79(6): 672-678, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37981939
4.
Evaluation of a flow cytometric test for G6PD-deficient erythrocytes.
Trop Med Int Health
; 26(4): 462-468, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33415798
5.
Hematological characteristics, cytogenetic features, and post-induction measurable residual disease in thymic stromal lymphopoietin receptor (TSLPR) overexpressed B-cell acute lymphoblastic leukemia in an Indian cohort.
Ann Hematol
; 100(8): 2031-2041, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34159401
6.
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 ß-thalassemia.
Ann Hematol
; 99(9): 2019-2026, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32676731
7.
Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/ß-Thalassemia Trait.
Hemoglobin
; 44(3): 211-213, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32448026
8.
Misdiagnosis of double heterozygous εGγ(Aγδß)0-thalassemia/ß++ thalassemia as homozygous ß-thalassemia: A pitfall for molecular diagnostic laboratories.
Blood Cells Mol Dis
; 81: 102394, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31821987
9.
HbH disease due to compound heterozygosity for hemoglobins Zürich-Albisrieden and Sallanches.
Pediatr Blood Cancer
; 67(4): e28161, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31930682
10.
18F-FDG PET/CT in Graft Versus Host Disease-Associated Polymyositis.
Clin Nucl Med
; 45(2): e106-e107, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31693622
11.
Anomaly of iliac veins: a rare cause of transient hepatic attenuation difference in a child.
Pediatr Radiol
; 39(11): 1242-5, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19672587
12.
ß-thalassemia intermedia mimicking ß-thalassemia trait: The importance of family studies and HBB genotyping in phenotypically ambiguous cases.
Int J Lab Hematol
; 45(4): 609-612, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36811326
13.
First reported co-occurrence of "GATA1-mutated X-linked thrombocytopenia with thalassemia (XLTT)" with heterozygous ß-thalassemia.
Int J Lab Hematol
; 45(6): 999-1002, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37382348
14.
Chronic eosinophilic leukemia with recurrent STAT5B N642H mutation-An entity with features of myelodysplastic syndrome/ myeloproliferative neoplasm overlap.
Leuk Res
; 112: 106753, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34856508
15.
The frequency, hematological characteristics, and end-of induction residual disease in B-acute lymphoblastic leukemia with BCR-ABL1-like chimeric gene fusions in a high-risk cohort from India.
Leuk Lymphoma
; 63(10): 2474-2478, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34027795
16.
Hb Brugg [HBA1:c.63C>A]: Report of an Ultra-Rare Variant Hemoglobin and Its Co-inheritance with Hb D-Punjab.
Indian J Hematol Blood Transfus
; 37(2): 326-328, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33867742
17.
Molecular Characterization of G6PD Deficiency at a North Indian Centre: Implications for Diagnostic Testing Laboratories in Different Regions of India.
Indian J Hematol Blood Transfus
; 36(4): 766-768, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-33100726