Hira JK - Search Results

1

β-thalassemia intermedia mimicking β-thalassemia trait: The importance of family studies and HBB genotyping in phenotypically ambiguous cases.

Singh N, Hira JK, Chhabra S, Das R, Khadwal AR, Sharma P. Singh N, et al. Among authors: hira jk. Int J Lab Hematol. 2023 Aug;45(4):609-612. doi: 10.1111/ijlh.14047. Epub 2023 Feb 22. Int J Lab Hematol. 2023. PMID: 36811326 No abstract available.

2

Hb M-Iwate in an Indian family.

Kumar GV, Sharma P, Chhabra S, Hira JK, Trehan A, Das R. Kumar GV, et al. Among authors: hira jk. Clin Chim Acta. 2015 Jun 15;446:192-4. doi: 10.1016/j.cca.2015.04.031. Epub 2015 Apr 27. Clin Chim Acta. 2015. PMID: 25931326

3

β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian Population.

Sreedharanunni S, Chhabra S, Hira JK, Bansal D, Sharma P, Das R. Sreedharanunni S, et al. Among authors: hira jk. Hemoglobin. 2015;39(5):362-5. doi: 10.3109/03630269.2015.1064004. Epub 2015 Aug 13. Hemoglobin. 2015. PMID: 26291970

4

High prevalence of VKORC1*3 (G9041A) genetic polymorphism in north Indians: A study on patients with cardiac disorders on acenocoumarol.

Sehgal T, Hira JK, Ahluwalia J, Das R, Vijayvergiya R, Rana SS, Varma N. Sehgal T, et al. Among authors: hira jk. Drug Discov Ther. 2015 Dec;9(6):404-10. doi: 10.5582/ddt.2015.01066. Drug Discov Ther. 2015. PMID: 26781925 Free article.

5

HbQ-India (HBA1:c.193G>C): hematological profiles and unique CE-HPLC findings of potential diagnostic utility in 65 cases.

Sharma S, Sharma P, Das R, Chhabra S, Hira JK. Sharma S, et al. Among authors: hira jk. Ann Hematol. 2017 Jul;96(7):1227-1229. doi: 10.1007/s00277-017-3020-z. Epub 2017 May 19. Ann Hematol. 2017. PMID: 28526955 No abstract available.

6

Misdiagnosis of double heterozygous ε^Gγ(^Aγδβ)⁰-thalassemia/β⁺⁺ thalassemia as homozygous β-thalassemia: A pitfall for molecular diagnostic laboratories.

Singh N, Hira JK, Chhabra S, Khadwal AR, Das R, Sharma P. Singh N, et al. Among authors: hira jk. Blood Cells Mol Dis. 2020 Mar;81:102394. doi: 10.1016/j.bcmd.2019.102394. Epub 2019 Nov 30. Blood Cells Mol Dis. 2020. PMID: 31821987 No abstract available.

7

HbH disease due to compound heterozygosity for hemoglobins Zürich-Albisrieden and Sallanches.

Sharma P, Das R, Khadwal AR, Karmakar I, Hira JK, Chhabra S. Sharma P, et al. Among authors: hira jk. Pediatr Blood Cancer. 2020 Apr;67(4):e28161. doi: 10.1002/pbc.28161. Epub 2020 Jan 13. Pediatr Blood Cancer. 2020. PMID: 31930682 No abstract available.

8

Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait.

Sharma P, Jandial A, Rajasekaran S, Das R, Chhabra S, Hira JK, Khadwal AR, Malhotra P, Sharma P. Sharma P, et al. Among authors: hira jk. Hemoglobin. 2020 May;44(3):211-213. doi: 10.1080/03630269.2020.1767128. Epub 2020 May 25. Hemoglobin. 2020. PMID: 32448026

9

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.

Shrestha O, Khadwal AR, Singhal M, Trehan A, Bansal D, Jain R, Pal A, Hira JK, Chhabra S, Malhotra P, Das R, Sharma P. Shrestha O, et al. Among authors: hira jk. Ann Hematol. 2020 Sep;99(9):2019-2026. doi: 10.1007/s00277-020-04176-2. Epub 2020 Jul 16. Ann Hematol. 2020. PMID: 32676731

10

Hb Brugg [HBA1:c.63C>A]: Report of an Ultra-Rare Variant Hemoglobin and Its Co-inheritance with Hb D-Punjab.

Sharma A, Das R, Khadwal AR, Hira JK, Chhabra S, Kumar V, Sharma P. Sharma A, et al. Among authors: hira jk. Indian J Hematol Blood Transfus. 2021 Apr;37(2):326-328. doi: 10.1007/s12288-020-01331-7. Epub 2020 Aug 10. Indian J Hematol Blood Transfus. 2021. PMID: 33867742 Free PMC article. No abstract available.

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