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Page 1
Clinical and genetic characterisation of a large Indian congenital myasthenic syndrome cohort.
Polavarapu K, Sunitha B, Töpf A, Preethish-Kumar V, Thompson R, Vengalil S, Nashi S, Bardhan M, Sanka SB, Huddar A, Unnikrishnan G, Arunachal G, Girija MS, Porter A, Azuma Y, Lorenzoni PJ, Baskar D, Anjanappa RM, Keertipriya M, Padmanabh H, Harikrishna GV, Laurie S, Matalonga L, Horvath R, Nalini A, Lochmüller H. Polavarapu K, et al. Among authors: baskar d. Brain. 2024 Jan 4;147(1):281-296. doi: 10.1093/brain/awad315. Brain. 2024. PMID: 37721175 Free PMC article.
A Rare Case of Eosinophilic Myelitis Due to Gnathostomiasis.
Baskar D, Nashi S, Reddy A, Vangayalapati S, Arshad F, Srijithesh PR, Kulkarni G, Alladi S, Wallop P, Ketboonlue T, Dekumyoy P. Baskar D, et al. Neurol India. 2022 Jan-Feb;70(1):395-398. doi: 10.4103/0028-3886.338692. Neurol India. 2022. PMID: 35263926 Free article.
Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India.
Nashi S, Polavarapu K, Bardhan M, Anjanappa RM, Preethish-Kumar V, Vengalil S, Padmanabha H, Geetha TS, Prathyusha PV, Ramprasad V, Joshi A, Chawla T, Unnikrishnan G, Sharma P, Huddar A, Uppilli B, Thomas A, Baskar D, Mathew S, Menon D, Arunachal G, Faruq M, Thangaraj K, Nalini A. Nashi S, et al. Among authors: baskar d. Neurogenetics. 2023 Jan;24(1):43-53. doi: 10.1007/s10048-022-00707-3. Epub 2022 Dec 29. Neurogenetics. 2023. PMID: 36580222
Classical Hirayama Disease Presenting as Progressive Spastic Quadriparesis.
Oommen AT, Vengalil S, Baskar D, Thomas A, Kulanthaivelu K, Bardhan M, Bhargava SS, Nalini A. Oommen AT, et al. Among authors: baskar d. Ann Indian Acad Neurol. 2023 May-Jun;26(3):308-310. doi: 10.4103/aian.aian_922_22. Epub 2023 Feb 23. Ann Indian Acad Neurol. 2023. PMID: 37538421 Free PMC article. No abstract available.
58 results