Bardhan M - Search Results

1

Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations.

Sanga S, Ghosh A, Kumar K, Polavarapu K, Preethish-Kumar V, Vengalil S, Nashi S, Bardhan M, Arunachal G, Raju S, Gayathri N, Biswas NK, Chakrabarti S, Nalini A, Roy S, Acharya M. Sanga S, et al. Among authors: bardhan m. Eur J Neurol. 2021 Mar;28(3):992-1003. doi: 10.1111/ene.14616. Epub 2020 Nov 26. Eur J Neurol. 2021. PMID: 33124102

2

An overview of the therapeutic strategies for neoplastic meningitis due to breast cancer: when and why?

Bardhan M, Dey D, Suresh V, Javed B, Venur VA, Joe N, Kalidindi R, Ozair A, Khan M, Mahtani R, Lo S, Odia Y, Ahluwalia MS. Bardhan M, et al. Expert Rev Neurother. 2024 Jan-Jun;24(1):77-103. doi: 10.1080/14737175.2023.2293223. Epub 2024 Jan 8. Expert Rev Neurother. 2024. PMID: 38145503 Review.

3

Immunological and inflammatory effects of infectious diseases in circadian rhythm disruption and future therapeutic directions.

Huang H, Mehta A, Kalmanovich J, Anand A, Bejarano MC, Garg T, Khan N, Tonpouwo GK, Shkodina AD, Bardhan M. Huang H, et al. Among authors: bardhan m. Mol Biol Rep. 2023 Apr;50(4):3739-3753. doi: 10.1007/s11033-023-08276-w. Epub 2023 Jan 19. Mol Biol Rep. 2023. PMID: 36656437 Free PMC article. Review.

4

Exploring Health Care Disparities in Genetic Testing and Research for Hereditary Cardiomyopathy: Current State and Future Perspectives.

Huang H, Verma J, Mok V, Bharadwaj HR, Alrawashdeh MM, Aratikatla A, Sudan S, Talukder S, Habaka M, Tse G, Bardhan M. Huang H, et al. Among authors: bardhan m. Glob Med Genet. 2024 Feb 1;11(1):36-47. doi: 10.1055/s-0044-1779469. eCollection 2024 Jan. Glob Med Genet. 2024. PMID: 38304308 Free PMC article. Review.

5

Zavegepant for Acute Treatment of Migraine: A Systematic Review and Meta-analysis of Randomized Controlled Trials.

Suresh V, Bardhan M, Dave T, Shamim MA, Suresh D, Satish P, Dhakal B, Bhonsale A, Roy P, Padhi BK, Monteith T. Suresh V, et al. Among authors: bardhan m. Clin Neuropharmacol. 2024 May-Jun 01;47(3):72-81. doi: 10.1097/WNF.0000000000000588. Clin Neuropharmacol. 2024. PMID: 38743600

6

The advent of RNA-based therapeutics for metabolic syndrome and associated conditions: a comprehensive review of the literature.

Huang HYR, Badar S, Said M, Shah S, Bharadwaj HR, Ramamoorthy K, Alrawashdeh MM, Haroon F, Basit J, Saeed S, Aji N, Tse G, Roy P, Bardhan M. Huang HYR, et al. Among authors: bardhan m. Mol Biol Rep. 2024 Apr 5;51(1):493. doi: 10.1007/s11033-024-09457-x. Mol Biol Rep. 2024. PMID: 38580818 Review.

7

Pharmacological and Non-pharmacological Approaches for the Management of Neuropathic Pain in Multiple Sclerosis.

Shkodina AD, Bardhan M, Chopra H, Anyagwa OE, Pinchuk VA, Hryn KV, Kryvchun AM, Boiko DI, Suresh V, Verma A, Delva MY. Shkodina AD, et al. Among authors: bardhan m. CNS Drugs. 2024 Mar;38(3):205-224. doi: 10.1007/s40263-024-01072-5. Epub 2024 Feb 29. CNS Drugs. 2024. PMID: 38421578 Review.

8

Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes - A recognizable clinical phenotype.

Polavarapu K, Vengalil S, Preethish-Kumar V, Arunachal G, Nashi S, Mohan D, Chawla T, Bardhan M, Nandeesh B, Gupta P, Gowda VK, Lochmüller H, Nalini A. Polavarapu K, et al. Among authors: bardhan m. Eur J Paediatr Neurol. 2021 Mar;31:54-60. doi: 10.1016/j.ejpn.2021.02.005. Epub 2021 Feb 16. Eur J Paediatr Neurol. 2021. PMID: 33631708

9

Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome.

Bardhan M, Polavarapu K, Bevinahalli NN, Veeramani PK, Anjanappa RM, Arunachal G, Shingavi L, Vengalil S, Nashi S, Chawla T, Nagabushana D, Mohan D, Horvath R, Nishino I, Atchayaram N. Bardhan M, et al. J Hum Genet. 2021 Aug;66(8):813-823. doi: 10.1038/s10038-021-00913-1. Epub 2021 Mar 12. J Hum Genet. 2021. PMID: 33712684

10

Correction: Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome.

Bardhan M, Polavarapu K, Bevinahalli NN, Preethish-Kumar V, Anjanappa RM, Arunachal G, Shingavi L, Vengalil S, Nashi S, Chawla T, Nagabushana D, Mohan D, Horvath R, Nishino I, Nalini A. Bardhan M, et al. J Hum Genet. 2021 Aug;66(8):841. doi: 10.1038/s10038-021-00920-2. J Hum Genet. 2021. PMID: 33767318 No abstract available.

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