Siris Patel
National Health Mission
Sambalpur, OR, India
Sambalpur, OR, India
Last Updated: 09/26/2026
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Found 26 publications
Influence of Alpha Thalassaemia on Hematological and Clinical Presentations in Patients of Sickle Cell-β-Thalassaemia with IVS I-5 (G→C) Mutation (HBB: C.20A > T/HBB: C.92 + 5G > C).
Journal: Hemoglobin
Published: October 31, 2025
Effect of α+ Thalassemia on the Severity of Plasmodium falciparum Malaria in Different Sickle Cell Genotypes in Indian Adults: A Hospital-Based Study.
Journal: Hemoglobin
Published: May 01, 2023
Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India.
Journal: Hemoglobin
Published: March 04, 2022
Iron profile of pregnant sickle cell anemia patients in Odisha, India.
Journal: Hematology, transfusion and cell therapy
Published: December 03, 2020
Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India.
Journal: Hemoglobin
Published: June 14, 2019
Pregnancy outcomes in women with sickle cell disease: a retrospective study from Eastern India.
Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: April 26, 2019
Association of fetal hemoglobin level with frequency of acute pain episodes in sickle cell disease (HbS-only phenotype) patients.
Journal: Blood cells, molecules & diseases
Published: September 06, 2018
Compound heterozygote of Hb DIran [HBB: c.67G>C, β 22(B4) Glu>Gln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India.
Journal: Hematology, transfusion and cell therapy
Published: September 01, 2017
Last Updated: 09/26/2026