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Page 1
Partial loss of desmin expression due to a leaky splice site variant in the human DES gene is associated with neuromuscular transmission defects.
Polavarapu K, O'Neil D, Thompson R, Spendiff S, Nandeesh B, Vengalil S, Huddar A, Baskar D, Arunachal G, Kotambail A, Bhatia S, Tumulu SK, Matalonga L, Töpf A, Laurie S, Zeldin J, Nashi S, Unnikrishnan G, Nalini A, Lochmüller H. Polavarapu K, et al. Among authors: huddar a. Neuromuscul Disord. 2024 Mar 22;39:10-18. doi: 10.1016/j.nmd.2024.03.011. Online ahead of print. Neuromuscul Disord. 2024. PMID: 38669730
Qualitative and Quantitative Electrocardiogram Parameters in a Large Cohort of Children with Duchenne Muscle Dystrophy in Comparison with Age-Matched Healthy Subjects: A Study from South India.
Girija MS, Menon D, Polavarapu K, Preethish-Kumar V, Vengalil S, Nashi S, Keertipriya M, Bardhan M, Thomas PT, Kiran VR, Nishadham V, Sadasivan A, Huddar A, Unnikrishnan GK, Inbaraj G, Krishnamurthy A, Kramer BW, Sathyaprabha TN, Nalini A. Girija MS, et al. Among authors: huddar a. Ann Indian Acad Neurol. 2024 Jan-Feb;27(1):53-57. doi: 10.4103/aian.aian_989_23. Epub 2024 Feb 6. Ann Indian Acad Neurol. 2024. PMID: 38495238 Free PMC article.
Monomelic Amyotrophy/Hirayama Disease: Surgical Outcome in a Large Cohort of Indian Patients.
Vengalil S, Pruthi N, Bhat D, Uppar AM, Polavarapu K, Preethish-Kumar V, Nashi S, Rajesh S, Aswini NS, Behera BP, Vandhiyadevan GD, Prasad C, Baskar D, Kulanthaivelu K, Saravanan A, Kandavel T, Nishadham V, Huddar A, Unnikrishnan G, Thomas A, Keerthipriya MS, Sanka SB, Manjunath N, Valasani RK, Bardhan M, Nalini A. Vengalil S, et al. Among authors: huddar a. World Neurosurg. 2024 Mar;183:e88-e97. doi: 10.1016/j.wneu.2023.11.087. Epub 2023 Nov 23. World Neurosurg. 2024. PMID: 38006932
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: huddar a. Brain. 2024 Jan 4;147(1):281-296. doi: 10.1093/brain/awad315. Brain. 2024. PMID: 37721175
Acute Fatal Leukoencephalopathic Presentation of CADASIL.
Huddar A, Seshagiri DV, Nandeesh B, Kulanthaivelu K, Gorantla P, Kenchaiah R. Huddar A, et al. Can J Neurol Sci. 2023 May 19:1-3. doi: 10.1017/cjn.2023.54. Online ahead of print. Can J Neurol Sci. 2023. PMID: 37203454 No abstract available.
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: huddar a. Neurogenetics. 2023 Jan;24(1):43-53. doi: 10.1007/s10048-022-00707-3. Epub 2022 Dec 29. Neurogenetics. 2023. PMID: 36580222
PET-MRI in idiopathic inflammatory myositis: a comparative study of clinical and immunological markers with imaging findings.
Girija MS, Tiwari R, Vengalil S, Nashi S, Preethish-Kumar V, Polavarapu K, Kulanthaivelu K, Arbind A, Bardhan M, Huddar A, Unnikrishnan G, Kiran VR, Chawla T, Nandeesh B, Nagaraj C, Nalini A. Girija MS, et al. Among authors: huddar a. Neurol Res Pract. 2022 Oct 10;4(1):49. doi: 10.1186/s42466-022-00213-9. Neurol Res Pract. 2022. PMID: 36210472 Free PMC article.
Cross-Sectional Area Reference Values of Nerves in the Upper and Lower Extremities using Ultrasonography in the Indian Population.
Sindhu DM, Huddar A, Saini J, Vengalil S, Nashi S, Bardhan M, Unnikrishnan G, Rajula RR, Kandavel T, Bathala L, Visser LH, Nalini A. Sindhu DM, et al. Among authors: huddar a. Ann Indian Acad Neurol. 2022 May-Jun;25(3):449-456. doi: 10.4103/aian.aian_727_21. Epub 2022 Apr 1. Ann Indian Acad Neurol. 2022. PMID: 35936619 Free PMC article.
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