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De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.
Pande S, Majethia P, Nair K, Rao LP, Mascarenhas S, Kaur N, do Rosario MC, Neethukrishna K, Chaurasia A, Hunakunti B, Jadhav N, Xavier S, Kumar J, Bhat V, Bhavani GS, Narayanan DL, Yatheesha BL, Patil SJ, Nampoothiri S, Kamath N, Aroor S, Bhat Y R, Lewis LE, Sharma S, Bajaj S, Sankhyan N, Siddiqui S, Nayak SS, Bielas S, Girisha KM, Shukla A. Pande S, et al. Among authors: kamath n. Eur J Hum Genet. 2023 Dec 20. doi: 10.1038/s41431-023-01513-7. Online ahead of print. Eur J Hum Genet. 2023. PMID: 38114583
Chromobacterium violaceum septicemia.
Shenoy S, Baliga S, Wilson G, Kamath N. Shenoy S, et al. Among authors: kamath n. Indian J Pediatr. 2002 Apr;69(4):363-4. doi: 10.1007/BF02723225. Indian J Pediatr. 2002. PMID: 12019559
Kawasaki syndrome in coastal India.
Kamath N, Shenoy R. Kamath N, et al. Indian Pediatr. 2007 Aug;44(8):623-4. Indian Pediatr. 2007. PMID: 17827642 Free article. No abstract available.
SIADH complicating deep neck abscess in infancy.
Shenoy RD, Nair S, Kamath N. Shenoy RD, et al. Among authors: kamath n. Int J Pediatr Otorhinolaryngol. 2005 Aug;69(8):1113-6. doi: 10.1016/j.ijporl.2005.02.012. Epub 2005 Mar 21. Int J Pediatr Otorhinolaryngol. 2005. PMID: 16005353
Recurrent and novel GLB1 mutations in India.
Bidchol AM, Dalal A, Trivedi R, Shukla A, Nampoothiri S, Sankar VH, Danda S, Gupta N, Kabra M, Hebbar SA, Bhat RY, Matta D, Ekbote AV, Puri RD, Phadke SR, Gowrishankar K, Aggarwal S, Ranganath P, Sharda S, Kamate M, Datar CA, Bhat K, Kamath N, Shah H, Krishna S, Gopinath PM, Verma IC, Nagarajaram HA, Satyamoorthy K, Girisha KM. Bidchol AM, et al. Among authors: kamath n. Gene. 2015 Aug 10;567(2):173-81. doi: 10.1016/j.gene.2015.04.078. Epub 2015 Apr 30. Gene. 2015. PMID: 25936995
156 results