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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.
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.
Cri du chat syndrome: a series of five cases.
Dangare HM, Oommen SP, Sheth AN, Koshy B, Roshan R, Thomas MM, Danda S, Srivastava VM. Dangare HM, et al. Among authors: danda s. Indian J Pathol Microbiol. 2012 Oct-Dec;55(4):501-5. doi: 10.4103/0377-4929.107791. Indian J Pathol Microbiol. 2012. PMID: 23455788
Menkes disease and response to copper histidine: An Indian case series.
Yoganathan S, Sudhakar SV, Arunachal G, Thomas M, Subramanian A, George R, Danda S. Yoganathan S, et al. Among authors: danda s. Ann Indian Acad Neurol. 2017 Jan-Mar;20(1):62-68. doi: 10.4103/0972-2327.199907. Ann Indian Acad Neurol. 2017. PMID: 28298846 Free PMC article.
156 results