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Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3.
Sim JC, Scerri T, Fanjul-Fernández M, Riseley JR, Gillies G, Pope K, van Roozendaal H, Heng JI, Mandelstam SA, McGillivray G, MacGregor D, Kannan L, Maixner W, Harvey AS, Amor DJ, Delatycki MB, Crino PB, Bahlo M, Lockhart PJ, Leventer RJ. Sim JC, et al. Among authors: kannan l. Ann Neurol. 2016 Jan;79(1):132-7. doi: 10.1002/ana.24502. Epub 2015 Dec 12. Ann Neurol. 2016. PMID: 26285051
Symptomatic neurocutaneous melanosis in a child.
Jain P, Kannan L, Kumar A, Sigamani E, Suri V, Basheer N, Suri A, Gulati S. Jain P, et al. Among authors: kannan l. JAMA Neurol. 2013 Apr;70(4):516. doi: 10.1001/jamaneurol.2013.2230. JAMA Neurol. 2013. PMID: 23420073 No abstract available.
Worcester drought syndrome - a form of bulbar cerebral palsy.
Jain P, Kannan L, Kumar A, Gulati S. Jain P, et al. Among authors: kannan l. Indian J Pediatr. 2013 May;80(5):436-7. doi: 10.1007/s12098-012-0932-4. Epub 2012 Dec 21. Indian J Pediatr. 2013. PMID: 23255080 No abstract available.
Role of Video-EEG in Children.
Kannan L, Jain P, Nayak D. Kannan L, et al. Indian J Pediatr. 2021 Oct;88(10):1007-1016. doi: 10.1007/s12098-020-03605-4. Epub 2021 Jan 4. Indian J Pediatr. 2021. PMID: 33394298 Review.
147 results