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

Year Number of Results
1966 3
1968 1
1972 4
1978 2
1979 1
1982 3
1983 1
1984 3
1985 5
1986 3
1987 2
1988 7
1989 4
1990 2
1991 2
1992 2
1993 4
1994 4
1995 5
1996 11
1997 5
1998 4
1999 4
2000 6
2001 6
2002 2
2003 5
2004 8
2005 3
2006 9
2007 12
2008 14
2009 10
2010 22
2011 18
2012 21
2013 22
2014 21
2015 27
2016 30
2017 28
2018 33
2019 47
2020 48
2021 40
2022 47
2023 42
2024 11

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548 results

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Page 1
Showing results for narayanan v[au]
Your search for Narayanam V[au] retrieved no results
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Masnada S, Hedrich UBS, Gardella E, Schubert J, Kaiwar C, Klee EW, Lanpher BC, Gavrilova RH, Synofzik M, Bast T, Gorman K, King MD, Allen NM, Conroy J, Ben Zeev B, Tzadok M, Korff C, Dubois F, Ramsey K, Narayanan V, Serratosa JM, Giraldez BG, Helbig I, Marsh E, O'Brien M, Bergqvist CA, Binelli A, Porter B, Zaeyen E, Horovitz DD, Wolff M, Marjanovic D, Caglayan HS, Arslan M, Pena SDJ, Sisodiya SM, Balestrini S, Syrbe S, Veggiotti P, Lemke JR, Møller RS, Lerche H, Rubboli G. Masnada S, et al. Among authors: narayanan v. Brain. 2017 Sep 1;140(9):2337-2354. doi: 10.1093/brain/awx184. Brain. 2017. PMID: 29050392 Free article.
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity.
Ernst ME, Baugh EH, Thomas A, Bier L, Lippa N, Stong N, Mulhern MS, Kushary S, Akman CI, Heinzen EL, Yeh R, Bi W, Hanchard NA, Burrage LC, Leduc MS, Chong JSC, Bend R, Lyons MJ, Lee JA, Suwannarat P, Brilstra E, Simon M, Koopmans M, van Binsbergen E, Groepper D, Fleischer J, Nava C, Keren B, Mignot C, Mathieu S, Mancini GMS, Madan-Khetarpal S, Infante EM, Bluvstein J, Seeley A, Bachman K, Klee EW, Schultz-Rogers LE, Hasadsri L, Barnett S, Ellingson MS, Ferber MJ, Narayanan V, Ramsey K, Rauch A, Joset P, Steindl K, Sheehan T, Poduri A, Vasquez A, Ruivenkamp C, White SM, Pais L, Monaghan KG, Goldstein DB, Sands TT, Aggarwal V. Ernst ME, et al. Among authors: narayanan v. Epilepsia. 2021 Jul;62(7):e103-e109. doi: 10.1111/epi.16931. Epub 2021 May 26. Epilepsia. 2021. PMID: 34041744 Free PMC article.
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.
Zawerton A, Mignot C, Sigafoos A, Blackburn PR, Haseeb A, McWalter K, Ichikawa S, Nava C, Keren B, Charles P, Marey I, Tabet AC, Levy J, Perrin L, Hartmann A, Lesca G, Schluth-Bolard C, Monin P, Dupuis-Girod S, Guillen Sacoto MJ, Schnur RE, Zhu Z, Poisson A, El Chehadeh S, Alembik Y, Bruel AL, Lehalle D, Nambot S, Moutton S, Odent S, Jaillard S, Dubourg C, Hilhorst-Hofstee Y, Barbaro-Dieber T, Ortega L, Bhoj EJ, Masser-Frye D, Bird LM, Lindstrom K, Ramsey KM, Narayanan V, Fassi E, Willing M, Cole T, Salter CG, Akilapa R, Vandersteen A, Canham N, Rump P, Gerkes EH, Klein Wassink-Ruiter JS, Bijlsma E, Hoffer MJV, Vargas M, Wojcik A, Cherik F, Francannet C, Rosenfeld JA, Machol K, Scott DA, Bacino CA, Wang X, Clark GD, Bertoli M, Zwolinski S, Thomas RH, Akay E, Chang RC, Bressi R, Sanchez Russo R, Srour M, Russell L, Goyette AE, Dupuis L, Mendoza-Londono R, Karimov C, Joseph M, Nizon M, Cogné B, Kuechler A, Piton A; Deciphering Developmental Disorder Study; Klee EW, Lefebvre V, Clark KJ, Depienne C. Zawerton A, et al. Among authors: narayanan v. Genet Med. 2020 Mar;22(3):524-537. doi: 10.1038/s41436-019-0657-0. Epub 2019 Oct 3. Genet Med. 2020. PMID: 31578471 Free PMC article.
Treatise of Thanatology.
Narayanan V. Narayanan V. Indian J Palliat Care. 2021 Oct-Dec;27(4):580-582. doi: 10.25259/IJPC_106_21. Epub 2021 Oct 28. Indian J Palliat Care. 2021. PMID: 34898956 Free PMC article. No abstract available.
Nano-Therapeutics to Treat Acne Vulgaris.
Chakraborty N, Narayanan V, Gautam HK. Chakraborty N, et al. Among authors: narayanan v. Indian J Microbiol. 2022 Jun;62(2):167-174. doi: 10.1007/s12088-022-01001-4. Epub 2022 Jan 29. Indian J Microbiol. 2022. PMID: 35462720 Free PMC article. Review.
GABRG2 Variants Associated with Febrile Seizures.
Hernandez CC, Shen Y, Hu N, Shen W, Narayanan V, Ramsey K, He W, Zou L, Macdonald RL. Hernandez CC, et al. Among authors: narayanan v. Biomolecules. 2023 Feb 22;13(3):414. doi: 10.3390/biom13030414. Biomolecules. 2023. PMID: 36979350 Free PMC article.
Friedreich's ataxia.
Alper G, Narayanan V. Alper G, et al. Among authors: narayanan v. Pediatr Neurol. 2003 May;28(5):335-41. doi: 10.1016/s0887-8994(03)00004-3. Pediatr Neurol. 2003. PMID: 12878293 Review.
Misleading "non-rasayanas".
Kukkupuni SK, Narayanan VS. Kukkupuni SK, et al. Among authors: narayanan vs. Pharmacogn Rev. 2015 Jan-Jun;9(17):84-5. doi: 10.4103/0973-7847.156359. Pharmacogn Rev. 2015. PMID: 26009698 Free PMC article. No abstract available.
Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders.
Burglen L, Van Hoeymissen E, Qebibo L, Barth M, Belnap N, Boschann F, Depienne C, De Clercq K, Douglas AGL, Fitzgerald MP, Foulds N, Garel C, Helbig I, Held K, Horn D, Janssen A, Kaindl AM, Narayanan V, Prager C, Rupin-Mas M, Afenjar A, Zhao S, Ramaekers VT, Ruggiero SM, Thomas S, Valence S, Van Maldergem L, Rohacs T, Rodriguez D, Dyment D, Voets T, Vriens J. Burglen L, et al. Among authors: narayanan v. Elife. 2023 Jan 17;12:e81032. doi: 10.7554/eLife.81032. Elife. 2023. PMID: 36648066 Free PMC article.
Silver Nanomaterials for Wound Dressing Applications.
Krishnan PD, Banas D, Durai RD, Kabanov D, Hosnedlova B, Kepinska M, Fernandez C, Ruttkay-Nedecky B, Nguyen HV, Farid A, Sochor J, Narayanan VHB, Kizek R. Krishnan PD, et al. Among authors: narayanan vhb. Pharmaceutics. 2020 Aug 28;12(9):821. doi: 10.3390/pharmaceutics12090821. Pharmaceutics. 2020. PMID: 32872234 Free PMC article. Review.
548 results