Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Karoni Dutt"'
Autor:
Bin Tang, Karoni Dutt, Ligia Papale, Raffaella Rusconi, Anupama Shankar, Jessica Hunter, Sergio Tufik, Frank H. Yu, William A. Catterall, Massimo Mantegazza, Alan L. Goldin, Andrew Escayg
Publikováno v:
Neurobiology of Disease, Vol 35, Iss 1, Pp 91-102 (2009)
Mutations in the voltage-gated sodium channel SCN1A are responsible for a number of seizure disorders including Generalized Epilepsy with Febrile Seizures Plus (GEFS+) and Severe Myoclonic Epilepsy of Infancy (SMEI). To determine the effects of SCN1A
Externí odkaz:
https://doaj.org/article/efa7f28a105f467082a33230c92c7409
Autor:
Andrew Escayg, George Andrew S Inglis, Alan L. Goldin, Sandra M. Garraway, Xiangmin Xu, Karoni Dutt, Steven F. Grieco, Lujia Chen, Jacquelyn T. Thelin, Jennifer C. Wong, Shangrila Parvin
Publikováno v:
Neuropsychopharmacology
Patients with SCN8A epileptic encephalopathy exhibit a range of clinical features, including multiple seizure types, movement disorders, and behavioral abnormalities, such as developmental delay, mild-to-severe intellectual disability, and autism. Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::657e06f61c4383bc86d759a12dde4dd0
https://pubmed.ncbi.nlm.nih.gov/33658654
https://pubmed.ncbi.nlm.nih.gov/33658654
Autor:
Ligia A. Papale, Karoni Dutt, Sandra L. Helmers, Alan L. Goldin, Stacey B. B. Dutton, Andrew Escayg
Publikováno v:
Dutton, SBB; Dutt, K; Papale, LA; Helmers, S; Goldin, AL; & Escayg, A. (2017). Early-life febrile seizures worsen adult phenotypes in Scn1a mutants. EXPERIMENTAL NEUROLOGY, 293, 159-171. doi: 10.1016/j.expneurol.2017.03.026. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/2d6880qf
Mutations in the voltage-gated sodium channel (VGSC) gene SCN1A, encoding the Nav1.1 channel, are responsible for a number of epilepsy disorders including genetic epilepsy with febrile seizures plus (GEFS+) and Dravet syndrome (DS). Patients with SCN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d22cd3d7c5aa5f5e7c0acbaae6ffefa7
https://europepmc.org/articles/PMC5538963/
https://europepmc.org/articles/PMC5538963/
Autor:
Alan L. Goldin, Frank G. Lin, Ligia A. Papale, Robert C. Liu, Karoni Dutt, Anupama Shankar, Andrew Escayg, Christopher D. Makinson, Arthur J. Barela
Publikováno v:
Makinson, CD; Dutt, K; Lin, F; Papale, LA; Shankar, A; Barela, AJ; et al.(2016). An Scn1a epilepsy mutation in Scn8a alters seizure susceptibility and behavior. Experimental Neurology, 275, 46-58. doi: 10.1016/j.expneurol.2015.09.008. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/11t2366n
Experimental neurology, vol 275 Pt 1, iss 0 1
Experimental neurology, vol 275 Pt 1, iss 0 1
© 2015 Elsevier Inc. Understanding the role of SCN8A in epilepsy and behavior is critical in light of recently identified human SCN8A epilepsy mutations. We have previously demonstrated that Scn8amedand Scn8amed-jomice carrying mutations in the Scn8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a59eeae6b4a2e060db2ef33184cc1609
https://escholarship.org/uc/item/11t2366n
https://escholarship.org/uc/item/11t2366n
Autor:
Sergio Tufik, Frank H. Yu, Andrew Escayg, Bin Tang, Anupama Shankar, Ligia A. Papale, Jessica Ezzell Hunter, Karoni Dutt, Raffaella Rusconi, William A. Catterall, Alan L. Goldin, Massimo Mantegazza
Publikováno v:
Neurobiology of Disease, Vol 35, Iss 1, Pp 91-102 (2009)
Mutations in the voltage-gated sodium channel SCN1A are responsible for a number of seizure disorders including Generalized Epilepsy with Febrile Seizures Plus (GEFS+) and Severe Myoclonic Epilepsy of Infancy (SMEI). To determine the effects of SCN1A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d1b85c295a19e0e5bae97a305dea0e0
http://www.sciencedirect.com/science/article/pii/S0969996109000849
http://www.sciencedirect.com/science/article/pii/S0969996109000849
Autor:
Stacey B. B. Dutton, Sergio Tufik, Georgius de Haan, Alan L. Goldin, Melinda S. Martin, Ligia A. Papale, Andrew Escayg, Anupama Shankar, Karoni Dutt, Miriam H. Meisler, Tallie Z. Baram, Céline Dubé
Voltage-gated sodium channels are required for the initiation and propagation of action potentials. Mutations in the neuronal voltage-gated sodium channel SCN1A are associated with a growing number of disorders including generalized epilepsy with feb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d1b4c0d54d3b4907244f5a8777ebeb4
https://europepmc.org/articles/PMC2843231/
https://europepmc.org/articles/PMC2843231/