Santhosh-Kumar R - Search Results

1

Sangeeth TA, Padmanabha H, Santhosh-Kumar R, Chandra SR, Dhar D, Mailankody P, Santosh V. Sangeeth TA, et al. Among authors: santhosh kumar r. J Pediatr. 2021 Apr;231:284-285. doi: 10.1016/j.jpeds.2020.12.017. Epub 2020 Dec 15. J Pediatr. 2021. PMID: 33333116 No abstract available.

2

Skin biopsy as an aid to diagnosis of disorders of the nervous system without cutaneous manifestations.

George M, Noone ML, Santhosh P, Santhoshkumar R, Sagar BKC, Mahadevan A. George M, et al. Int J Dermatol. 2021 Oct;60(10):1179-1182. doi: 10.1111/ijd.15513. Epub 2021 Mar 12. Int J Dermatol. 2021. PMID: 33709389 Review.

3

Electron microscopy in the diagnosis of skeletal muscle disorders: Its utility and limitations.

Santhoshkumar R, Narayanappa G. Santhoshkumar R, et al. Indian J Pathol Microbiol. 2022 May;65(Supplement):S291-S299. doi: 10.4103/ijpm.ijpm_1113_21. Indian J Pathol Microbiol. 2022. PMID: 35562161 Free article. Review.

4

Foot-and-mouth disease virus induces PERK-mediated autophagy to suppress the antiviral interferon response.

Ranjitha HB, Ammanathan V, Guleria N, Hosamani M, Sreenivasa BP, Dhanesh VV, Santhoshkumar R, Sagar BKC, Mishra BP, Singh RK, Sanyal A, Manjithaya R, Basagoudanavar SH. Ranjitha HB, et al. J Cell Sci. 2020 Jul 9;134(5):jcs240622. doi: 10.1242/jcs.240622. J Cell Sci. 2020. PMID: 32482793

5

Frontal lobe epilepsy with focal neuronal lipofuscinosis - Case report of a rare entity.

Mhatre R, Jagtap SA, Kurwale N, Santhoshkumar R, Deshmukh Y, Mahadevan A. Mhatre R, et al. Epilepsy Behav Rep. 2020 May 21;14:100369. doi: 10.1016/j.ebr.2020.100369. eCollection 2020. Epilepsy Behav Rep. 2020. PMID: 32743541 Free PMC article.

6

A Dominant C150Y Mutation in FHL1 Induces Structural Alterations in LIM2 Domain Causing Protein Aggregation In Human and Drosophila Indirect Flight Muscles.

Santhoshkumar R, Preethish-Kumar V, Mangalaparthi KK, Unni S, Padmanabhan B, T S KP, Nongthomba U, Atchayaram N, Narayanappa G. Santhoshkumar R, et al. J Mol Neurosci. 2021 Nov;71(11):2324-2335. doi: 10.1007/s12031-020-01777-4. Epub 2021 Jan 30. J Mol Neurosci. 2021. PMID: 33515430

7

[No title available]

[No authors listed] [No authors listed] PMID: 34005325

8

A Novel L1 Linker Mutation in DES Resulted in Total Absence of Protein.

Santhoshkumar R, Preethish-Kumar V, Polavarapu K, Reghunathan D, Chaudhari S, Satyamoorthy K, Vengalil S, Nashi S, Faruq M, Joshi A, Atchayaram N, Narayanappa G. Santhoshkumar R, et al. J Mol Neurosci. 2021 Dec;71(12):2468-2473. doi: 10.1007/s12031-021-01856-0. Epub 2021 Jun 9. J Mol Neurosci. 2021. PMID: 34106405

9

Neurodegeneration with brain iron accumulation: Characterization of clinical, radiological, and genetic features of pediatric patients from Southern India.

Bhardwaj NK, Gowda VK, Saini J, Sardesai AV, Santhoshkumar R, Mahadevan A. Bhardwaj NK, et al. Brain Dev. 2021 Nov;43(10):1013-1022. doi: 10.1016/j.braindev.2021.06.010. Epub 2021 Jul 14. Brain Dev. 2021. PMID: 34272103

10

Infection of human microglial cell line CHME-3 to study neuropathogenesis of chikungunya virus.

Qadri SW, Kumar N, Santhoshkumar R, Desai A, Ravi V, Venkataswamy MM. Qadri SW, et al. J Neurovirol. 2022 Jun;28(3):374-382. doi: 10.1007/s13365-022-01070-7. Epub 2022 Mar 29. J Neurovirol. 2022. PMID: 35352315

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