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

Year Number of Results
2006 1
2007 1
2008 3
2009 3
2010 3
2011 5
2012 10
2013 4
2014 9
2015 10
2016 10
2017 9
2018 7
2019 9
2020 11
2021 18
2022 22
2023 10
2024 8

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128 results

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Page 1
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.
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.
Novel Mutations in CRLF1: Case Reports with Crisponi Syndrome.
A R, Chandran S, Ghatak AR, Thomas N, Danda S. A R, et al. Among authors: danda s. Indian J Pediatr. 2022 Nov;89(11):1148-1150. doi: 10.1007/s12098-022-04263-4. Epub 2022 Aug 19. Indian J Pediatr. 2022. PMID: 35984556 Review.
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.
An Inherited Cause of Stroke Mimic in a Toddler.
Yoganathan S, Kumar M, Sushma L, Danda S, Thomas M. Yoganathan S, et al. Among authors: danda s. Indian J Pediatr. 2022 Jan;89(1):98. doi: 10.1007/s12098-021-03904-4. Epub 2021 Sep 1. Indian J Pediatr. 2022. PMID: 34468936 No abstract available.
Fumaric Aciduria: A Rare Cause of Refractory Epilepsy.
Yoganathan S, Srinivasaraghavan R, Kumar M, Kratz L, Mular S, Sudhakar SV, Malik P, Chandran M, Thomas M, Danda S. Yoganathan S, et al. Among authors: danda s. Ann Indian Acad Neurol. 2022 Jul-Aug;25(4):738-740. doi: 10.4103/aian.aian_47_22. Epub 2022 Sep 9. Ann Indian Acad Neurol. 2022. PMID: 36211164 Free PMC article. No abstract available.
Eye signs in a child with ROBO3 gene mutation.
Yoganathan S, Kumar M, Malhotra M, Joy P, Danda S, Thomas M, David KS, Jasper A, Selvin SST. Yoganathan S, et al. Among authors: danda s. Indian J Ophthalmol. 2022 Jul;70(7):2643-2644. doi: 10.4103/ijo.IJO_2065_21. Indian J Ophthalmol. 2022. PMID: 35791185 Free PMC article. No abstract available.
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.
128 results