Network abnormalities and interneuron dysfunction in Alzheimer disease

Cites (261)

Items 201–261 of 261

1. Amyloid-β-Induced Action Potential Desynchronization and Degradation of Hippocampal Gamma Oscillations Is Prevented by Interference with Peptide Conformation Change and Aggregation
   Firoz Roshan Kurudenkandy, Misha Y. Zilberter, Henrik Biverstål, Jenny Presto, Dmytro Honcharenko, Roger Strömberg, Jan Johansson, Bengt G. Winblad, André Fisahn · 2014 · Journal of Neuroscience
2. A new mechanism for antiepileptic drug action: vesicular entry may mediate the effects of levetiracetam
   Anna L. Meehan, Xiaofeng Yang, Brian D. McAdams, Li‐Lian Yuan, Steven M. Rothman · 2011 · Journal of Neurophysiology
3. Seizures in dominantly inherited Alzheimer disease
   Aline Zaréa, Camille Charbonnier, Anne Rovelet‐Lecrux, Gaël Nicolas, Stéphane Rousseau, Alaina Borden, Jérémie Pariente, Isabelle Le Ber, Florence Pasquier, Maïté Formaglio et al. · 2016 · Neurology
4. Neuronal Structure is Altered by Amyloid Plaques
   Tara L. Spires‐Jones, Bradley T. Hyman · 2004 · Reviews in the Neurosciences
5. Epileptic Seizures in Alzheimer Disease
   Andras Attila Horvath, Anna Szűcs, Gábor Barcs, Jeffrey L. Noebels, Anita Kamondi · 2016 · Alzheimer Disease & Associated Disorders
6. Orchestrated experience-driven Arc responses are disrupted in a mouse model of Alzheimer's disease
   Rudinskiy, Nikita, Hawkes, Jonathan M, Betensky, Rebecca A, Eguchi, Megumi, Yamaguchi, Shun, Spires-Jones, Tara L, Hyman, Bradley T · 2012 · Nature Neuroscience
7. Neuronal Network Oscillations in Neurodegenerative Diseases
   Volker Nimmrich, Andreas Draguhn, Nikolai Axmacher · 2015 · NeuroMolecular Medicine
8. Neuroinflammation in Alzheimer’s Disease: from Pathogenesis to a Therapeutic Target
   Sanjay W. Pimplikar · 2014 · Journal of Clinical Immunology
9. Altered deactivation in individuals with genetic risk for Alzheimer's disease
   Persson, J., Lind, J., Larsson, A., Ingvar, M., Sleegers, K., Van Broeckhoven, C., Adolfsson, R., Nilsson, L.-G., Nyberg, L. · 2008 · Neuropsychologia
10. Hyperexcitability and epileptic seizures in a model of frontotemporal dementia
    Ana M. García-Cabrero, Rosa Guerrero, Beatriz G. Giráldez, Marı́a Llorens-Martı́n, Jesús Ávila, José María Serratosa, Marina P. Sánchez · 2013 · Neurobiology of Disease
11. Accelerated aging of the GABAergic septohippocampal pathway and decreased hippocampal rhythms in a mouse model of Alzheimer's disease
    Rubio, Sara E., Vega‐Flores, Germán, Martínez, Albert, Bosch, Carles, Pérez‐Mediavilla, Alberto, Río, Joaquín del, Gruart, Agnès, Delgado‐García, José María, Soriano, Eduardo, Pascual, Marta · 2012 · The FASEB Journal
12. Brivaracetam, but not ethosuximide, reverses memory impairments in an Alzheimer’s disease mouse model
    Haakon B. Nygaard, Adam C. Kaufman, Tomoko Sekine-Konno, Linda L. Huh, Hilary Going, Samantha J. Feldman, Mikhail A. Kostylev, Stephen M. Strittmatter · 2015 · Alzheimer s Research & Therapy
13. Sodium Channel Cleavage Is Associated with Aberrant Neuronal Activity and Cognitive Deficits in a Mouse Model of Alzheimer's Disease
    Brian F. Corbett, Steven C. Leiser, Huai‐Ping Ling, Reka Nagy, Nathalie Breysse, Xiaohong Zhang, Anupam Hazra, Jon T. Brown, Andrew D. Randall, Andrew Wood et al. · 2013 · Journal of Neuroscience
14. Apolipoprotein E4 produced in GABAergic interneurons causes learning and memory deficits in mice
    Knoferle, Johanna, Yoon, Seo Yeon, Walker, David, Leung, Laura, Gillespie, Anna K., Tong, Leslie M., Bien-Ly, Nga, Huang, Yadong · 2014 · The Journal of Neuroscience
15. Evidence for dysregulated high-frequency oscillations during sensory processing in medication-naïve, first episode schizophrenia
    Sun, Limin, Castellanos, Nazareth, Grützner, Christine, Koethe, Dagmar, Rivolta, Davide, Wibral, Michael, Kranaster, Laura, Singer, Wolf, Leweke, Markus F., Uhlhaas, Peter J. · 2013 · Schizophrenia Research
16. Cortical Excitatory State and Variability in Human Brain Rhythms
    Herbert H. Jasper · 1936 · Science
17. APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage
    Anne Rovelet‐Lecrux, Thierry Frébourg, Hannu J. Tuominen, Kari Majamaa, Dominique Campion, Anne Marja Remes · 2007 · Journal of Neurology Neurosurgery & Psychiatry
18. Neurodegeneration in Alzheimer's disease: caspases and synaptic element interdependence
    Dale E. Bredesen · 2009 · Molecular Neurodegeneration
19. EEG alterations in non-demented individuals related to apolipoprotein E genotype and to risk of Alzheimer disease
    Н.В. Пономарева, Г. И. Коровайцева, Evgeny Ivanovich Rogaev · 2007 · Neurobiology of Aging
20. Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series
    Daniel McNaughton, William D. Knight, Rita João Guerreiro, Natalie Sarah Ryan, Jessica Lowe, Mark Poulter, David Joseph Nicholl, John Hardy, Tamás Révész, James S Lowe et al. · 2010 · Neurobiology of Aging
21. Hilar GABAergic Interneuron Activity Controls Spatial Learning and Memory Retrieval
    Yaisa S. Andrews-Zwilling, Anna K. Gillespie, Alexxai V. Kravitz, Alexandra Nelson, Nino Devidze, Iris Lo, Seo Yeon Yoon, Nga Bien‐Ly, Karen L. Ring, Daniel Zwilling et al. · 2012 · PLoS ONE
22. Epileptic Discharges Affect the Default Mode Network – fMRI and Intracerebral EEG Evidence
    Firas Fahoum, Rina Zelmann, Louise Tyvaert, François Dubeau, Jean Gotman · 2013 · PLoS ONE
23. Clinical comparison of Alzheimer's disease in pedigrees with the codon 717 Val→Ile mutation in the amyloid precursor protein gene
    MICHAEL J. MULLAN, Shoji Tsuji, T. Miki, Tomohiro Katsuya, Satoshi Naruse, K. Kaneko, T. Shimizu, Takeshi Kojima, Imaharu Nakano, Toshio Ogihara et al. · 1993 · Neurobiology of Aging
24. Spike bursts increase amyloid-β 40/42 ratio by inducing a presenilin-1 conformational change
    Iftach Dolev, Hilla Fogel, Hila Milshtein-Parush, Yevgeny Berdichevsky, Noa Lipstein, Nils Brose, Neta Gazit, Inna Slutsky · 2013 · Nature Neuroscience
25. Increased Cortical and Thalamic Excitability in Freely Moving APPswe/PS1dE9 Mice Modeling Epileptic Activity Associated with Alzheimer's Disease
    Kestutis Gurevicius, Arto Lipponen, Heikki Tanila · 2012 · Cerebral Cortex
26. Enkephalin Elevations Contribute to Neuronal and Behavioral Impairments in a Transgenic Mouse Model of Alzheimer's Disease
    William J. Meilandt, Gui-Qiu Yu, Jeannie Chin, Erik D. Roberson, Jorge J. Palop, Tiffany Z. Wu, Kimberly A. Scearce-Levie, Lennart Mucke · 2008 · Journal of Neuroscience
27. Network oscillations modulate interictal epileptiform spike rate during human memory
    Joseph Y. Matsumoto, Matt Stead, Michał Tomasz Kucewicz, Andrew J. Matsumoto, Pierce A. Peters, Benjamin H. Brinkmann, Jane C. Danstrom, Stephan J. Goerss, W. Richard Marsh, Fred B. Meyer et al. · 2013 · Brain
28. 40-Hz steady state response in Alzheimer's disease and mild cognitive impairment
    Jeroen A. van Deursen, Eric F. P. M. Vuurman, Vivianne H.J.M. van Kranen-Mastenbroek, Frans R.J. Verhey, Wim J. Riedel · 2009 · Neurobiology of Aging
29. Impairment of hippocampal gamma (γ)‐frequency oscillations in vitro in mice overexpressing human amyloid precursor protein (APP)
    Joanne E. Driver, Claudia Racca, Mark O. Cunningham, Stephen K. Towers, Ceri H. Davies, Miles A. Whittington, Fiona E. N. LeBeau · 2007 · European Journal of Neuroscience
30. Presenilin-1 mutation Alzheimer's disease: A genetic epilepsy syndrome?
    Andrew J. Larner · 2011 · Epilepsy & Behavior
31. p38 MAP kinase-mediated NMDA receptor-dependent suppression of hippocampal hypersynchronicity in a mouse model of Alzheimer’s disease
    Arne Ittner, Amadeus Gladbach, Josefine Bertz, Lisa S. Suh, Lars Matthias Ittner · 2014 · Acta Neuropathologica Communications
32. Phenotypic Profile of Early-Onset Familial Alzheimer's Disease Caused by Presenilin-1 E280A Mutation
    Sepulveda-Falla, Diego, Glatzel, Markus, Lopera, Francisco · 2012 · Journal of Alzheimer's Disease
33. Familial Alzheimer's disease A pedigree with a mis-sense mutation in the amyloid precursor protein gene (amyloid precursor protein 717 valine → glycine)
    Angus M Kennedy, Sarah Newman, Andrew McCaddon, Joanna A. Ball, Penelope K. Roques, MICHAEL J. MULLAN, John Hardy, Marie‐Christine Chartier‐Harlin, Richard S. J. Frackowiak, Elizabeth K. Warrington et al. · 1993 · Brain
34. Altered Theta Oscillations and Aberrant Cortical Excitatory Activity in the 5XFAD Model of Alzheimer’s Disease
    Siwek, Magdalena Elisabeth, Müller, Ralf, Henseler, Christina, Trog, Astrid, Lundt, Andreas, Wormuth, Carola, Broich, Karl, Ehninger, Dan, Weiergräber, Marco, Papazoglou, Anna · 2015 · Neural Plasticity
35. Seizures and dementia in the elderly: Nationwide Inpatient Sample 1999–2008
    Dean Sherzai, Travis E. Losey, Sonia Vega, Ayesha Z. Sherzai · 2014 · Epilepsy & Behavior
36. New Criteria for Alzheimer Disease and Mild Cognitive Impairment
    Andrew E. Budson, Paul R. Solomon · 2012 · The Neurologist
37. Network dysfunction in<i>α</i>‐synuclein transgenic mice and human Lewy body dementia
    Morris, Meaghan, Sanchez, Pascal E., Verret, Laure, Beagle, Alexander J., Guo, Weikun, Dubal, Dena, Ranasinghe, Kamalini G., Koyama, Akihiko, Ho, Kaitlyn, Yu, Gui‐Qiu et al. · 2015 · Annals of Clinical and Translational Neurology
38. fMRI activation during episodic encoding and metacognitive appraisal across the lifespan: Risk factors for Alzheimer's disease
    Mehul Alkesh Trivedi, Taylor W. Schmitz, Michele L. Ries, Timothy Hess, Michele E. Fitzgerald, Craig Atwood, Howard A. Rowley, Sanjay Asthana, Mark A. Sager, Sterling C. Johnson · 2007 · Neuropsychologia
39. Default mode network alterations during language task performance in children with benign epilepsy with centrotemporal spikes (BECTS)
    Nadine Oser, Martina Hubacher, Karsten Specht, Alexandre Datta, Peter Weber, Iris‐Katharina Penner · 2014 · Epilepsy & Behavior
40. A Large Swedish Family With Alzheimer's Disease With a Codon 670/671 Amyloid Precursor Protein Mutation
    Karin Axelman · 1994 · Archives of Neurology
41. Anti-Aβ antibodies incapable of reducing cerebral Aβ oligomers fail to attenuate spatial reference memory deficits in J20 mice
    Alexandra J. Mably, Wen Liu, Jessica M. Mc Donald, Jean‐Cosme Dodart, Frédérique Bard, Cynthia Ann Lemere, Brian O’Nuallain, Dominic M. Walsh · 2015 · Neurobiology of Disease
42. Basal GABA regulates GABA(B)R conformation and release probability at single hippocampal synapses.
    Tal Laviv, I. Riven, Iftach Dolev, Irena Vertkin, B. Balana, P. Slesinger, I. Slutsky · 2010 · Neuron
43. Clinical Course of Patients with Familial Early-Onset Alzheimer’s Disease Potentially Lacking Senile Plaques Bearing the E693Δ Mutation in Amyloid Precursor Protein
    Hiroyuki Shimada, Suzuka Ataka, Takami Tomiyama, Hajime Takechi, Hiroshi Mori, Takami Miki · 2011 · Dementia and Geriatric Cognitive Disorders
44. Wide Range of Disease Onset in a Family With Alzheimer Disease and a His163Tyr Mutation in the Presenilin-1 Gene
    Karin Axelman, Hans Basun, Lars Lannfelt · 1998 · Archives of Neurology
45. Therapeutic potential of NaV1.1 activators
    Henrik S. Jensen, Morten Grunnet, Jesper F. Bastlund · 2014 · Trends in Pharmacological Sciences
46. The developmental changes of Nav1.1 and Nav1.2 expression in the human hippocampus and temporal lobe
    Wang, Wenze, Takashima, Sachio, Segawa, Yoshie, Itoh, Masayuki, Shi, Xiuyu, Hwang, Su-Kyeong, Nabeshima, Kazuki, Takeshita, Morishige, Hirose, Shinichi · 2011 · Brain Research
47. Oxygen Level and LFP in Task-Positive and Task-Negative Areas: Bridging BOLD fMRI and Electrophysiology
    William J. Bentley, Jingfeng M. Li, Abraham Z. Snyder, Marcus E. Raichle, Lawrence H. Snyder · 2014 · Cerebral Cortex
48. Emergence of a seizure phenotype in aged apolipoprotein epsilon 4 targeted replacement mice
    Hunter, Jesse M., Cirrito, John R., Restivo, Jessica L., Kinley, Robert D., Sullivan, Patrick M., Holtzman, David M., Koger, Deanna, Delong, Cynthia, Lin, Suizhen, Zhao, Lingzhi et al. · 2012 · Brain Research
49. An African American family with early-onset Alzheimer disease and an APP (T714I) mutation
    Terri A. Edwards-Lee, John Matthew Ringman, Julia A. Chung, John S. Werner, Angharad R. Morgan, Peter St George‐Hyslop, Paul M. Thompson, Rebecca A. Dutton, Anton Mlikotic, Ekaterina A. Rogaeva et al. · 2005 · Neurology
50. Functional changes in glutamate transporters and astrocyte biophysical properties in a rodent model of focal cortical dysplasia
    Susan L. Campbell, John J. Hablitz, Michelle Lynne Olsen · 2014 · Frontiers in Cellular Neuroscience
51. Modulation of behavioral networks by selective interneuronal inactivation
    M J Schmidt, Szatmár Horváth, Philip J. Ebert, Jeremy L. Norris, Erin H. Seeley, Jacquelyn Ann Brown, Levente Gellért, Monika Everheart, Krassimira A. Garbett, T. W. Grice et al. · 2013 · Molecular Psychiatry
52. Amyloid Beta 1-42 Inhibits Entorhinal Cortex Activity in the Beta-Gamma Range: Role of GSK-3
    Fernando Peña‐Ortega, Angeles Solis-Cisneros, Benito Ordaz · 2012 · Current Alzheimer Research
53. Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy
    Anne Marja Remes, Saara Finnilä, Helinä Mononen, Hannu J. Tuominen, R. Takalo, Riitta Herva, Kari Majamaa · 2004 · Neurology
54. Shift in interictal relative gamma power as a novel biomarker for drug response in two mouse models of absence epilepsy
    Atul Maheshwari, Rachel L. Marks, Katherine M. Yu, Jeffrey L. Noebels · 2015 · Epilepsia
55. Medial temporal lobe default mode functioning and hippocampal structure as vulnerability indicators for schizophrenia: A MRI study of non-psychotic adolescent first-degree relatives
    Larry J. Seidman, Isabelle M. Rosso, Heidi W. Thermenos, Nikos Makris, Richard J. Juelich, John D. E. Gabrieli, Stephen V. Faraone, Ming T. Tsuang, Susan Whitfield · 2014 · Schizophrenia Research
56. Familial Alzheimer Disease: A Large, Multigeneration German Kindred
    Peter Frommelt, Ralf Schnabel, Wolfgang Kiihne · 1991 · Alzheimer Disease & Associated Disorders
57. Atypical early-onset Alzheimer's disease caused by the Iranian APP mutation
    Suzanne Granhøj Lindquist, Jørgen Erik Nielsen, Jette Stokholm, M. Schwartz, Mustafa Batbayli, Martin Ballegaard, Jesper Erdal, Katja Krabbe, Gunhild Waldemar · 2008 · Journal of the Neurological Sciences
58. Early onset Alzheimer's disease in a South American pedigree from Argentina
    Carlos Alberto Mangone, E. M. Castaño, Efrat Levy, G. Abiusi, Thomas Wısnıewskı, Maria Risoleta Freire Marques, E. Faccio, Philip B. Gorelick, Blas Frangione, Roberto E.P. Sica · 1995 · Acta Neurologica Scandinavica
59. A second family with familial AD and the V717L APP mutation has a later age at onset
    Alison K. Godbolt, Jon A. Beck, J. C. Collinge · 2006 · Neurology
60. The E280A Presenilin Mutation Reduces Voltage-Gated Sodium Channel Levels in Neuronal Cells
    Doo Yeon Kim, Mary H. Wertz, Vivek Gautam, Carla D’Avanzo, Raja Bhattacharyya, Dora M. Kovacs · 2013 · Neurodegenerative Diseases
61. Phenotypical difference of Amyloid Precursor Protein (APP) V717L mutation in Japanese family
    Masao Abe, Naomi Sonobe, Ryuji Fukuhara · 2012 · BMC Neurology