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Page 1
Morvan's Syndrome with Myasthenia Gravis: An Autoimmune or Paraneoplastic Association?
Menon D, Chakkera P, Jha S, Kumar BP, Anjusha JSS, Sena MC, Rao S, Arshad F, Nashi S, Vengalil S, Alladi S, Nalini A. Menon D, et al. Ann Indian Acad Neurol. 2024 Sep 1;27(5):612-615. doi: 10.4103/aian.aian_391_24. Epub 2024 Sep 20. Ann Indian Acad Neurol. 2024. PMID: 39445897 Free PMC article. No abstract available.
DYT30 due to VPS16 Mutation: An Etiology of Childhood-Onset Generalized Dystonia.
Shashi S, Nashi S, Arunachal G, Venkatachalam N, Padmanabha H, Mailankody P, Menon D, Arshad F, Alladi S, Mathuranath P, Mahale RR. Shashi S, et al. Among authors: menon d. Ann Indian Acad Neurol. 2023 May-Jun;26(3):286-288. doi: 10.4103/aian.aian_59_23. Epub 2023 Apr 20. Ann Indian Acad Neurol. 2023. PMID: 37538408 Free PMC article. No abstract available.
Atypical Presentation of Tangier Disease-Expanding the Clinical Spectrum.
Baskar D, Vengalil S, Nashi S, Menon D, Bevinahalli N N, Thomas A, Bardhan M, Sanka SB, Manjunath N, Nalini A. Baskar D, et al. Among authors: menon d. J Clin Neuromuscul Dis. 2023 Sep 1;25(1):42-45. doi: 10.1097/CND.0000000000000453. J Clin Neuromuscul Dis. 2023. PMID: 37611269
A novel DHTKD1 gene mutation with ALS like presentation: a case report.
Menon D, Nashi S, Mohanty M, Dubbal R, Mk F, Vengalil S, Thomas A, Kumar V, Baskar D, Arunachal G, Nalini A. Menon D, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2024 May;25(3-4):413-415. doi: 10.1080/21678421.2023.2273366. Epub 2023 Oct 25. Amyotroph Lateral Scler Frontotemporal Degener. 2024. PMID: 37880984
Sensory Neuropathy in Spinocerebellar Ataxia Type 14: A Novel Phenotype.
Nashi S, Singh R, Menon D, Arshad F, Alladi S, Mahale RR. Nashi S, et al. Among authors: menon d. Ann Indian Acad Neurol. 2023 Jul-Aug;26(4):591-593. doi: 10.4103/aian.aian_324_23. Epub 2023 Jun 8. Ann Indian Acad Neurol. 2023. PMID: 37970274 Free PMC article. No abstract available.
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: menon d. 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.
Phenotype-Genotype Correlation of a Cohort of Patients with Congenital Myopathy: A Single Centre Experience from India.
Harikrishna GV, Padmanabha H, Polavarapu K, Anjanappa RM, Preethish-Kumar V, Nandeesh BN, Vengalil S, Nashi S, Baskar D, Thomas A, Bardhan M, Arunachal G, Menon D, Sanka SB, Manjunath N, Nalini A. Harikrishna GV, et al. Among authors: menon d. J Neuromuscul Dis. 2024;11(5):935-957. doi: 10.3233/JND-230021. J Neuromuscul Dis. 2024. PMID: 38968056 Free PMC article.
1,372 results