Devendra R - Search Results

1

Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations.

Devendra R, Gupta V, Shanmugam R, Singh MPSS, Patel P, Valecha N, Mishra N, Ahmed N, Hoti SL, Hegde HV, Warang P, Chiddarwar A, Kedar P, Mayekar P, Mukherjee MB. Devendra R, et al. Infect Genet Evol. 2020 Dec;86:104597. doi: 10.1016/j.meegid.2020.104597. Epub 2020 Oct 16. Infect Genet Evol. 2020. PMID: 33069889

2

Does novel P5'N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?

Warang P, Devendra R, Chiddarwar A, Gupta V, Mirgal D, Jadli A, Mohite A, Kedar P, Mukherjee M. Warang P, et al. Among authors: devendra r. Blood Cells Mol Dis. 2017 Jul;66:8-10. doi: 10.1016/j.bcmd.2017.07.002. Epub 2017 Jul 20. Blood Cells Mol Dis. 2017. PMID: 28756180 No abstract available.

3

G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India.

Devendra R, Gupta V, Biradar SS, Bhat P, Hegde S, Hoti SL, Mukherjee MB, Hegde HV. Devendra R, et al. Ann Hum Biol. 2020 Feb;47(1):55-58. doi: 10.1080/03014460.2019.1699954. Epub 2019 Dec 13. Ann Hum Biol. 2020. PMID: 31833391

4

A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant.

Devendra R, Warang P, Gupta V, Chiddarwar A, Kedar P, Agarwal MB, Mukherjee MB. Devendra R, et al. Indian J Hematol Blood Transfus. 2019 Apr;35(2):399-401. doi: 10.1007/s12288-018-1049-3. Epub 2018 Dec 6. Indian J Hematol Blood Transfus. 2019. PMID: 30988594 Free PMC article. No abstract available.

5

Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?

Warang P, Devendra R, D'Silva S, Chiddarwar A, Kedar P, Ghosh K, Colah R, Mukherjee MB. Warang P, et al. Among authors: devendra r. Ann Hematol. 2015 Jan;94(1):169-71. doi: 10.1007/s00277-014-2123-z. Epub 2014 Jun 20. Ann Hematol. 2015. PMID: 24947795 No abstract available.

6

Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A).

Dongerdiye R, Kamat P, Jain P, Warang P, Devendra R, Wasekar N, Sharma R, Mhaskar K, Madkaikar MR, Manglani MV, Kedar PS. Dongerdiye R, et al. Among authors: devendra r. J Clin Pathol. 2019 Jun;72(6):393-398. doi: 10.1136/jclinpath-2019-205718. Epub 2019 Mar 27. J Clin Pathol. 2019. PMID: 30918013

7

Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction.

Kedar PS, Dongerdiye R, Chilwirwar P, Gupta V, Chiddarwar A, Devendra R, Warang P, Prasada H, Sampagar A, Bhat S, Chandrakala S, Madkaikar M. Kedar PS, et al. Among authors: devendra r. Indian J Pediatr. 2019 Aug;86(8):692-699. doi: 10.1007/s12098-019-02928-1. Epub 2019 Apr 27. Indian J Pediatr. 2019. PMID: 31030358

8

Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia.

Gupta V, Kulkarni A, Warang P, Devendra R, Chiddarwar A, Kedar P. Gupta V, et al. Among authors: devendra r. Hum Mutat. 2020 Apr;41(4):737-748. doi: 10.1002/humu.23973. Epub 2020 Jan 30. Hum Mutat. 2020. PMID: 31898843

9

Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.

More TA, Dongerdiye R, Devendra R, Warang PP, Kedar PS. More TA, et al. Among authors: devendra r. Ann Hematol. 2020 Apr;99(4):715-727. doi: 10.1007/s00277-020-03955-1. Epub 2020 Feb 28. Ann Hematol. 2020. PMID: 32112123

10

Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family.

Dongerdiye R, Jagadeesh S, Suresh B, Rajendran A, Devendra R, Warang P, Kedar PS. Dongerdiye R, et al. Among authors: devendra r. J Clin Pathol. 2021 Oct;74(10):620-624. doi: 10.1136/jclinpath-2020-206960. Epub 2020 Dec 25. J Clin Pathol. 2021. PMID: 33361148 Review.

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