Devendra R[au] - Search Results

Year	Number of Results
2012	3
2014	2
2015	1
2017	3
2018	1
2019	5
2020	7
2021	2
2022	1
2023	1

1

Investigations of catalysis of urethane formation using organotin dicarboxylate.

Devendra R, Edmonds NR, Söhnel T. Devendra R, et al. Heliyon. 2020 May 28;6(5):e04074. doi: 10.1016/j.heliyon.2020.e04074. eCollection 2020 May. Heliyon. 2020. PMID: 32490256 Free PMC article.

2

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.

3

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

4

Successful management of Methemoglobinemia and G6PD deficiency in a patient posted for surgical excision of branchial cyst.

Arun VJ, Deorukhkar A, Rafi AM, Charles D, Devendra R, Innah SJ, Kedar P. Arun VJ, et al. Among authors: devendra r. Asian J Transfus Sci. 2022 Jan-Jun;16(1):128-131. doi: 10.4103/ajts.ajts_152_20. Epub 2022 May 26. Asian J Transfus Sci. 2022. PMID: 36199403 Free PMC article.

5

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

6

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.

7

Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders.

More TA, Dalal B, Devendra R, Warang P, Shankarkumar A, Kedar P. More TA, et al. Among authors: devendra r. Cytometry B Clin Cytom. 2020 May;98(3):238-249. doi: 10.1002/cyto.b.21857. Epub 2019 Nov 21. Cytometry B Clin Cytom. 2020. PMID: 31750618 Free article.

8

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

9

Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family.

Dongerdiye R, Sampagar A, Devendra R, Warang P, Kedar P. Dongerdiye R, et al. Among authors: devendra r. BMC Med Genomics. 2021 Jul 28;14(1):191. doi: 10.1186/s12920-021-01038-2. BMC Med Genomics. 2021. PMID: 34321014 Free PMC article.

10

Gravity driven deterministic lateral displacement for particle separation in microfluidic devices.

Devendra R, Drazer G. Devendra R, et al. Anal Chem. 2012 Dec 18;84(24):10621-7. doi: 10.1021/ac302074b. Epub 2012 Nov 29. Anal Chem. 2012. PMID: 23137317

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