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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 2
2001 2
2005 1
2006 1
2007 2
2008 3
2009 3
2010 4
2011 6
2012 10
2013 7
2014 11
2015 11
2016 13
2017 10
2018 11
2019 9
2020 12
2021 21
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2025 13

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176 results

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Page 1
Proband only exome sequencing in 403 Indian children with neurodevelopmental disorders: Diagnostic yield, utility and challenges in a resource-limited setting.
Pranav Chand R, Vinit W, Vaidya V, Iyer AS, Shelke M, Aggarwal S, Magar S, Danda S, Moirangthem A, Phadke SR, Goyal M, Ranganath P, Mistri M, Shah P, Shah N, Kotecha UH. Pranav Chand R, et al. Among authors: danda s. Eur J Med Genet. 2023 May;66(5):104730. doi: 10.1016/j.ejmg.2023.104730. Epub 2023 Feb 15. Eur J Med Genet. 2023. PMID: 36801247 Review.
Restrictive Dermopathy.
Dutta AK, Danda S. Dutta AK, et al. Among authors: danda s. Pediatr Neonatol. 2016 Jun;57(3):259. doi: 10.1016/j.pedneo.2015.09.005. Epub 2015 Oct 28. Pediatr Neonatol. 2016. PMID: 26627141 Free article. No abstract available.
Authors' response.
Danda S, Thomas BM, Paramshivam G, Thomas R, Mathew J, Danda D. Danda S, et al. Indian J Med Res. 2020 Oct;152(4):430-431. doi: 10.4103/0971-5916.305172. Indian J Med Res. 2020. PMID: 33380712 Free PMC article. No abstract available.
Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from India.
Nagarajan B, Gowda VK, Yoganathan S, Sharawat IK, Srivastava K, Vora N, Badheka R, Danda S, Kalane U, Kaur A, Madaan P, Mehta S, Negi S, Panda PK, Rajadhyaksha S, Saini AG, Saini L, Shah S, Srinivasan VM, Suthar R, Thomas M, Vyas S, Sankhyan N, Sahu JK. Nagarajan B, et al. Among authors: danda s. Epilepsia Open. 2023 Dec;8(4):1383-1404. doi: 10.1002/epi4.12811. Epub 2023 Aug 25. Epilepsia Open. 2023. PMID: 37583270 Free PMC article.
SGCE Myoclonus-Dystonia: An Inherited Movement Disorder.
Yoganathan S, Kumar M, Sharma S, Patel S, Danda S, Thomas M. Yoganathan S, et al. Among authors: danda s. Neurology. 2022 Feb 15;98(7):289. doi: 10.1212/WNL.0000000000013209. Epub 2021 Dec 14. Neurology. 2022. PMID: 34906973 No abstract available.
Oculodigital Sign: A Clinical Clue for Diagnosis.
Yoganathan S, Kumar M, John D, Danda S, Oommen SP, Umakant SB, Thomas M. Yoganathan S, et al. Among authors: danda s. Ann Indian Acad Neurol. 2022 May-Jun;25(3):560-561. doi: 10.4103/aian.aian_755_21. Epub 2022 May 3. Ann Indian Acad Neurol. 2022. PMID: 35936593 Free PMC article. No abstract available.
KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literature.
Yoganathan S, Whitney R, Thomas M, Danda S, Chettali AM, Prasad AN, Farhan SMK, AlSowat D, Abukhaled M, Aldhalaan H, Gowda VK, Kinhal UV, Bylappa AY, Konanki R, Lingappa L, Parchuri BM, Appendino JP, Scantlebury MH, Cunningham J, Hadjinicolaou A, El Achkar CM, Kamate M, Menon RN, Jose M, Riordan G, Kannan L, Jain V, Manokaran RK, Chau V, Donner EJ, Costain G, Minassian BA, Jain P. Yoganathan S, et al. Among authors: danda s. Epilepsia. 2024 Mar;65(3):709-724. doi: 10.1111/epi.17880. Epub 2024 Jan 17. Epilepsia. 2024. PMID: 38231304
Van der Woude Syndrome: IRF6 Mutations.
Sunny AP, Arunachal G, Danda S. Sunny AP, et al. Among authors: danda s. Indian J Pediatr. 2019 Nov;86(11):1070-1071. doi: 10.1007/s12098-019-03058-4. Epub 2019 Aug 29. Indian J Pediatr. 2019. PMID: 31468312 No abstract available.
Childhood Neurological Disorders With Hyperhomocystinemia: A Case-Based Review.
Yoganathan S, Bhasin H, Garg D, Malik P, Saini AG, Chandran M, Korula S, Arunachal G, Danda S, Thomas M, Oommen SP, Sharma S. Yoganathan S, et al. Among authors: danda s. Pediatr Neurol. 2023 Sep;146:26-30. doi: 10.1016/j.pediatrneurol.2023.06.003. Epub 2023 Jun 13. Pediatr Neurol. 2023. PMID: 37413720
176 results