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Neuroradiological findings in GAA-FGF14 ataxia (SCA27B): more than cerebellar atrophy.
Chen S, Ashton C, Sakalla R, Clement G, Planel S, Bonnet C, Lamont P, Kulanthaivelu K, Nalini A, Houlden H, Duquette A, Dicaire MJ, Iruzubieta Agudo P, Ruiz Martinez J, de Lucas EM, Berjon RS, Infante Ceberio J, Indelicato E, Boesch S, Synofzik M, Bender B, Danzi MC, Zuchner S, Pellerin D, Brais B, Renaud M, La Piana R. Chen S, et al. Among authors: nalini a. medRxiv [Preprint]. 2024 Feb 18:2024.02.16.24302945. doi: 10.1101/2024.02.16.24302945. medRxiv. 2024. PMID: 38405699 Free PMC article. Preprint.
Bing Neel syndrome presenting as isolated cranial nerve palsies - a case report.
Baskar D, Anudeep DDS, Vengalil S, Patavaradhan P, Kulanthaivelu K, Tiwari R, Nandeesh BN, Sitani K, Raja P, Mundlamuri RC, Yadav R, Nalini A. Baskar D, et al. Among authors: nalini a. eNeurologicalSci. 2024 May 15;35:100505. doi: 10.1016/j.ensci.2024.100505. eCollection 2024 Jun. eNeurologicalSci. 2024. PMID: 38784860 Free PMC article.
Spastic quadriparesis in Fabry disease: A diagnostic challenge.
Jha S, Vengalil S, Ravindranadh CM, Nalini A, Yadav R. Jha S, et al. Among authors: nalini a. Natl Med J India. 2023 Sep-Oct;36(5):340-341. doi: 10.25259/NMJI_MS_133_21. Natl Med J India. 2023. PMID: 38759977 No abstract available.
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: nalini 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: nalini 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.
Myotonic Dystrophy Type 1 (DM1): Clinical Characteristics and Disease Progression in a Large Cohort.
Chawla T, Reddy N, Jankar R, Vengalil S, Polavarapu K, Arunachal G, Preethish-Kumar V, Nashi S, Bardhan M, Rajeshwaran J, Afsar M, Warrier M, Thomas PT, Thennarasu K, Nalini A. Chawla T, et al. Among authors: nalini a. Neurol India. 2024 Jan 1;72(1):83-89. doi: 10.4103/neuroindia.NI_1432_20. Epub 2024 Feb 29. Neurol India. 2024. PMID: 38443007 Free article.
218 results