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Novel insights into the genetic profile of hereditary spastic paraplegia in India.
Narendiran S, Debnath M, Shivaram S, Kannan R, Sharma S, Christopher R, Seshagiri DV, Jain S, Purushottam M, Mangalore S, Bharath RD, Bindu PS, Sinha S, Taly AB, Nagappa M. Narendiran S, et al. Among authors: sinha s. J Neurogenet. 2022 Mar;36(1):21-31. doi: 10.1080/01677063.2022.2064463. Epub 2022 May 2. J Neurogenet. 2022. PMID: 35499206
Treating mania in Wilson's disease with lithium.
Loganathan S, Nayak R, Sinha S, Taly AB, Math S, Varghese M. Loganathan S, et al. Among authors: sinha s. J Neuropsychiatry Clin Neurosci. 2008 Fall;20(4):487-9. doi: 10.1176/jnp.2008.20.4.487. J Neuropsychiatry Clin Neurosci. 2008. PMID: 19196936 No abstract available.
Cranial MRI in acute hyperammonemic encephalopathy.
Bindu PS, Sinha S, Taly AB, Christopher R, Kovoor JM. Bindu PS, et al. Among authors: sinha s. Pediatr Neurol. 2009 Aug;41(2):139-42. doi: 10.1016/j.pediatrneurol.2009.02.012. Pediatr Neurol. 2009. PMID: 19589465
6,470 results