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Page 1
Mitochondrial DNA variations in Madras motor neuron disease.
Govindaraj P, Nalini A, Krishna N, Sharath A, Khan NA, Tamang R, Gourie-Devi M, Brown RH, Thangaraj K. Govindaraj P, et al. Among authors: nalini a. Mitochondrion. 2013 Nov;13(6):721-8. doi: 10.1016/j.mito.2013.02.003. Epub 2013 Feb 16. Mitochondrion. 2013. PMID: 23419391 Free PMC article.
Novel TCAP mutation c.32C>A causing limb girdle muscular dystrophy 2G.
Francis A, Sunitha B, Vinodh K, Polavarapu K, Katkam SK, Modi S, Bharath MM, Gayathri N, Nalini A, Thangaraj K. Francis A, et al. Among authors: nalini a. PLoS One. 2014 Jul 23;9(7):e102763. doi: 10.1371/journal.pone.0102763. eCollection 2014. PLoS One. 2014. PMID: 25055047 Free PMC article.
Disrupted structural connectome and neurocognitive functions in Duchenne muscular dystrophy: classifying and subtyping based on Dp140 dystrophin isoform.
Preethish-Kumar V, Shah A, Polavarapu K, Kumar M, Safai A, Vengalil S, Nashi S, Deepha S, Govindaraj P, Afsar M, Rajeswaran J, Nalini A, Saini J, Ingalhalikar M. Preethish-Kumar V, et al. Among authors: nalini a. J Neurol. 2022 Apr;269(4):2113-2125. doi: 10.1007/s00415-021-10789-y. Epub 2021 Sep 10. J Neurol. 2022. PMID: 34505932
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.
Van Haute L, O'Connor E, Díaz-Maldonado H, Munro B, Polavarapu K, Hock DH, Arunachal G, Athanasiou-Fragkouli A, Bardhan M, Barth M, Bonneau D, Brunetti-Pierri N, Cappuccio G, Caruana NJ, Dominik N, Goel H, Helman G, Houlden H, Lenaers G, Mention K, Murphy D, Nandeesh B, Olimpio C, Powell CA, Preethish-Kumar V, Procaccio V, Rius R, Rebelo-Guiomar P, Simons C, Vengalil S, Zaki MS, Ziegler A, Thorburn DR, Stroud DA, Maroofian R, Christodoulou J, Gustafsson C, Nalini A, Lochmüller H, Minczuk M, Horvath R. Van Haute L, et al. Among authors: nalini a. Nat Commun. 2023 Feb 23;14(1):1009. doi: 10.1038/s41467-023-36277-7. Nat Commun. 2023. PMID: 36823193 Free PMC article.
Family Caregivers' Experiences with Dying and Bereavement of Individuals with Motor Neuron Disease in India.
Warrier MG, Thomas PT, Sadasivan A, Balasubramaniam B, Vengalil S, Nashi S, Preethish-Kumar V, Polavarapu K, Mahajan NP, Chevula PCR, Nalini A. Warrier MG, et al. Among authors: nalini a. J Soc Work End Life Palliat Care. 2019 Apr-Jun;15(2-3):111-125. doi: 10.1080/15524256.2019.1645081. Epub 2019 Aug 2. J Soc Work End Life Palliat Care. 2019. PMID: 31373263
Novel TBK1 variant associated with Frontotemporal Dementia overlap syndrome.
Arshad F, Vengalil S, Nalini A, Polavarapu K, Shamim U, Jabeen S, Nagaraj C, Ramakrishnan S, Faruq M, Alladi S. Arshad F, et al. Among authors: nalini a. Acta Neurol Scand. 2022 Apr;145(4):399-406. doi: 10.1111/ane.13562. Epub 2021 Nov 28. Acta Neurol Scand. 2022. PMID: 34841512
220 results