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Alex C. Bender, Ph.D. - Publications

Institution:
Dartmouth College, Hanover, NH, United States
Area:
epilepsy, pediatrics
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Bender AC, Jaleel A, Pellerin KR, Moguilner S, Sarkis R, Cash SS, Lam A. Altered Sleep Micro-architecture and Cognitive Impairment in Patients With Temporal Lobe Epilepsy. Neurology. PMID 37848332 DOI: 10.1212/WNL.0000000000207942  0.393
2020 Sakkaki S, Barrière S, Bender AC, Scott RC, Lenck-Santini PP. Focal Dorsal Hippocampal Nav1.1 Knock Down Alters Place Cell Temporal Coordination and Spatial Behavior. Cerebral Cortex (New York, N.Y. : 1991). PMID 32377688 DOI: 10.1093/Cercor/Bhaa101  0.601
2017 Bender AC, Austin AM, Grodstein F, Bynum JP. Executive function, episodic memory, and Medicare expenditures. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 28174070 DOI: 10.1016/J.Jalz.2016.12.013  0.486
2016 Bender AC, Luikart BW, Lenck-Santini PP. Cognitive Deficits Associated with Nav1.1 Alterations: Involvement of Neuronal Firing Dynamics and Oscillations. Plos One. 11: e0151538. PMID 26978272 DOI: 10.1371/Journal.Pone.0151538  0.683
2013 Bender AC, Natola H, Ndong C, Holmes GL, Scott RC, Lenck-Santini PP. Focal Scn1a knockdown induces cognitive impairment without seizures. Neurobiology of Disease. 54: 297-307. PMID 23318929 DOI: 10.1016/J.Nbd.2012.12.021  0.656
2012 Bender AC, Morse RP, Scott RC, Holmes GL, Lenck-Santini PP. SCN1A mutations in Dravet syndrome: impact of interneuron dysfunction on neural networks and cognitive outcome. Epilepsy & Behavior : E&B. 23: 177-86. PMID 22341965 DOI: 10.1016/J.Yebeh.2011.11.022  0.665
2012 Holmes GL, Bender AC, Wu EX, Scott RC, Lenck-Santini PP, Morse RP. Maturation of EEG oscillations in children with sodium channel mutations. Brain & Development. 34: 469-77. PMID 21940124 DOI: 10.1016/J.Braindev.2011.08.009  0.617
2010 Rosas HD, Lee SY, Bender AC, Zaleta AK, Vangel M, Yu P, Fischl B, Pappu V, Onorato C, Cha JH, Salat DH, Hersch SM. Altered white matter microstructure in the corpus callosum in Huntington's disease: implications for cortical "disconnection". Neuroimage. 49: 2995-3004. PMID 19850138 DOI: 10.1016/J.Neuroimage.2009.10.015  0.362
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