All Relations between Amyotrophic Lateral Sclerosis and hippocampus

Publication Sentence Publish Date Extraction Date Species
Foteini Christidi, Efstratios Karavasilis, Michail Rentzos, Georgios Velonakis, Vasiliki Zouvelou, Sofia Xirou, Georgios Argyropoulos, Ioannis Papatriantafyllou, Varvara Pantolewn, Panagiotis Ferentinos, Nikolaos Kelekis, Ioannis Seimenis, Ioannis Evdokimidis, Peter Bed. Neuroimaging data indicate divergent mesial temporal lobe profiles in amyotrophic lateral sclerosis, Alzheimer's disease and healthy aging. Data in brief. vol 28. 2020-10-01. PMID:31921944. "hippocampal pathology in amyotrophic lateral sclerosis: selective vulnerability of subfields and their associated projections" [1]. 2020-10-01 2023-08-13 human
Foteini Christidi, Efstratios Karavasilis, Michail Rentzos, Georgios Velonakis, Vasiliki Zouvelou, Sofia Xirou, Georgios Argyropoulos, Ioannis Papatriantafyllou, Varvara Pantolewn, Panagiotis Ferentinos, Nikolaos Kelekis, Ioannis Seimenis, Ioannis Evdokimidis, Peter Bed. Neuroimaging data indicate divergent mesial temporal lobe profiles in amyotrophic lateral sclerosis, Alzheimer's disease and healthy aging. Data in brief. vol 28. 2020-10-01. PMID:31921944. amyotrophic lateral sclerosis and alzheimer's disease exhibit divergent hippocampal profiles. 2020-10-01 2023-08-13 human
Judith Machts, Stefan Vielhaber, Katja Kollewe, Susanne Petri, Joern Kaufmann, Mircea Ariel Schoenfel. Global Hippocampal Volume Reductions and Local CA1 Shape Deformations in Amyotrophic Lateral Sclerosis. Frontiers in neurology. vol 9. 2020-09-30. PMID:30079050. global hippocampal volume reductions and local ca1 shape deformations in amyotrophic lateral sclerosis. 2020-09-30 2023-08-13 Not clear
Judith Machts, Stefan Vielhaber, Katja Kollewe, Susanne Petri, Joern Kaufmann, Mircea Ariel Schoenfel. Global Hippocampal Volume Reductions and Local CA1 Shape Deformations in Amyotrophic Lateral Sclerosis. Frontiers in neurology. vol 9. 2020-09-30. PMID:30079050. there is increasing evidence for hippocampal involvement in amyotrophic lateral sclerosis (als). 2020-09-30 2023-08-13 Not clear
Eoin Finegan, Stacey Li Hi Shing, Rangariroyashe H Chipika, Mary C McKenna, Mark A Doherty, Jennifer C Hengeveld, Alice Vajda, Colette Donaghy, Russell L McLaughlin, Siobhan Hutchinson, Orla Hardiman, Peter Bed. Thalamic, hippocampal and basal ganglia pathology in primary lateral sclerosis and amyotrophic lateral sclerosis: Evidence from quantitative imaging data. Data in brief. vol 29. 2020-09-28. PMID:32055654. thalamic, hippocampal and basal ganglia pathology in primary lateral sclerosis and amyotrophic lateral sclerosis: evidence from quantitative imaging data. 2020-09-28 2023-08-13 human
Eoin Finegan, Stacey Li Hi Shing, Rangariroyashe H Chipika, Mary C McKenna, Mark A Doherty, Jennifer C Hengeveld, Alice Vajda, Colette Donaghy, Russell L McLaughlin, Siobhan Hutchinson, Orla Hardiman, Peter Bed. Thalamic, hippocampal and basal ganglia pathology in primary lateral sclerosis and amyotrophic lateral sclerosis: Evidence from quantitative imaging data. Data in brief. vol 29. 2020-09-28. PMID:32055654. a standardised, prospective, single-centre neuroimaging protocol was used to characterise thalamic, hippocampal and basal ganglia involvement in 33 patients with primary lateral sclerosis (pls), 100 patients with amyotrophic lateral sclerosis (als), and 117 healthy controls. 2020-09-28 2023-08-13 human
Evgeny Shlevkov, Himanish Basu, Mark-Anthony Bray, Zheng Sun, Wei Wei, Kaan Apaydin, Kyle Karhohs, Pin-Fang Chen, Janell L M Smith, Ole Wiskow, Kasper Roet, Xuan Huang, Kevin Eggan, Anne E Carpenter, Robin J Kleiman, Thomas L Schwar. A High-Content Screen Identifies TPP1 and Aurora B as Regulators of Axonal Mitochondrial Transport. Cell reports. vol 28. issue 12. 2020-09-10. PMID:31533043. pharmacological inhibition or small hairpin rna (shrna) knockdown of each target promotes mitochondrial axonal transport in rat hippocampal neurons and induced pluripotent stem cell (ipsc)-derived human cortical neurons and enhances mitochondrial transport in ipsc-derived motor neurons from an amyotrophic lateral sclerosis (als) patient bearing one copy of sod1 2020-09-10 2023-08-13 human
J Mollink, M Hiemstra, K L Miller, I N Huszar, M Jenkinson, J Raaphorst, M Wiesmann, O Ansorge, M Pallebage-Gamarallage, A M van Cappellen van Walsu. White matter changes in the perforant path area in patients with amyotrophic lateral sclerosis. Neuropathology and applied neurobiology. vol 45. issue 6. 2020-08-31. PMID:31002412. the aim of this study was to test the hypothesis that white matter degeneration of the perforant path - as part of the papez circuit - is a key feature of amyotrophic lateral sclerosis (als), even in the absence of frontotemporal dementia (ftd) or deposition of ptdp-43 inclusions in hippocampal granule cells. 2020-08-31 2023-08-13 Not clear
Foteini Christidi, Efstratios Karavasilis, Michail Rentzos, Georgios Velonakis, Vasiliki Zouvelou, Sofia Xirou, Georgios Argyropoulos, Ioannis Papatriantafyllou, Varvara Pantolewn, Panagiotis Ferentinos, Nikolaos Kelekis, Ioannis Seimenis, Ioannis Evdokimidis, Peter Bed. Hippocampal pathology in amyotrophic lateral sclerosis: selective vulnerability of subfields and their associated projections. Neurobiology of aging. vol 84. 2020-08-06. PMID:31629116. hippocampal pathology in amyotrophic lateral sclerosis: selective vulnerability of subfields and their associated projections. 2020-08-06 2023-08-13 Not clear
Foteini Christidi, Efstratios Karavasilis, Michail Rentzos, Georgios Velonakis, Vasiliki Zouvelou, Sofia Xirou, Georgios Argyropoulos, Ioannis Papatriantafyllou, Varvara Pantolewn, Panagiotis Ferentinos, Nikolaos Kelekis, Ioannis Seimenis, Ioannis Evdokimidis, Peter Bed. Hippocampal pathology in amyotrophic lateral sclerosis: selective vulnerability of subfields and their associated projections. Neurobiology of aging. vol 84. 2020-08-06. PMID:31629116. although hippocampal involvement in amyotrophic lateral sclerosis (als) has been consistently highlighted by postmortem studies, memory impairment remains under-recognized and the involvement of specific hippocampal subfields and their connectivity patterns are poorly characterized in vivo. 2020-08-06 2023-08-13 Not clear
Yevgen Chornenkyy, David W Fardo, Peter T Nelso. Tau and TDP-43 proteinopathies: kindred pathologic cascades and genetic pleiotropy. Laboratory investigation; a journal of technical methods and pathology. vol 99. issue 7. 2020-06-25. PMID:30742063.  although tdp-43 proteinopathy was first described in the central nervous system of patients with amyotrophic lateral sclerosis (als) and in subtypes of frontotemporal dementia (ftd/ftld), tdp-43 proteinopathy is also present in chronic traumatic encephalopathy, cognitively impaired persons in advanced age with hippocampal sclerosis, huntington's disease, and other diseases. 2020-06-25 2023-08-13 human
Yuko Yamaguchi, Takashi Ayaki, Fangzhou Li, Atsushi Tsujimura, Masaki Kamada, Hidefumi Ito, Takakuni Maki, Nobukatsu Sawamoto, Makoto Urushitani, Ryosuke Takahash. Phosphorylated NF-κB subunit p65 aggregates in granulovacuolar degeneration and neurites in neurodegenerative diseases with tauopathy. Neuroscience letters. vol 704. 2020-02-05. PMID:30946927. in this study, we examined phosphorylated p65 (pp65), which is the activated form of a subunit of nuclear factor-kappa b (nf-κb), in the hippocampus of 21 autopsied cases, including ad, amyotrophic lateral sclerosis cases with optineurin mutation (als-optn), and a variety of other neurodegenerative disorder cases and normal controls. 2020-02-05 2023-08-13 Not clear
Stefan Stamenković, Tanja Dučić, Vera Stamenković, Alexander Kranz, Pavle R Andju. Imaging of glial cell morphology, SOD1 distribution and elemental composition in the brainstem and hippocampus of the ALS hSOD1 Neuroscience. vol 357. 2018-05-22. PMID:28576725. imaging of glial cell morphology, sod1 distribution and elemental composition in the brainstem and hippocampus of the als hsod1 amyotrophic lateral sclerosis (als) is a neurodegenerative disorder affecting motor and cognitive domains of the cns. 2018-05-22 2023-08-13 Not clear
Koichi Okamot. Ubiquitin-positive tau-negative intraneuronal inclusions in dementia with motor neuron disease: The 50th Anniversary of Japanese Society of Neuropathology. Neuropathology : official journal of the Japanese Society of Neuropathology. vol 30. issue 5. 2016-02-17. PMID:20500451. we first reported ubiquitin-positive tau-negative intraneuronal inclusions in the hippocampal granular cell layer and entorhinal cortices in patients with amyotrophic lateral sclerosis (als). 2016-02-17 2023-08-12 Not clear
J Raaphorst, M J van Tol, M de Visser, A J van der Kooi, C B Majoie, L H van den Berg, B Schmand, D J Veltma. Prose memory impairment in amyotrophic lateral sclerosis patients is related to hippocampus volume. European journal of neurology. vol 22. issue 3. 2015-12-03. PMID:25557180. prose memory impairment in amyotrophic lateral sclerosis patients is related to hippocampus volume. 2015-12-03 2023-08-13 Not clear
Susanne Abdulla, Judith Machts, Jörn Kaufmann, Karina Patrick, Katja Kollewe, Reinhard Dengler, Hans-Jochen Heinze, Susanne Petri, Stefan Vielhaber, Peter J Nesto. Hippocampal degeneration in patients with amyotrophic lateral sclerosis. Neurobiology of aging. vol 35. issue 11. 2015-10-19. PMID:25004891. hippocampal degeneration in patients with amyotrophic lateral sclerosis. 2015-10-19 2023-08-13 Not clear
Henk-Jan Westeneng, Esther Verstraete, Renée Walhout, Ruben Schmidt, Jeroen Hendrikse, Jan H Veldink, Martijn P van den Heuvel, Leonard H van den Ber. Subcortical structures in amyotrophic lateral sclerosis. Neurobiology of aging. vol 36. issue 2. 2015-09-21. PMID:25281019. the aim of this study was to assess the involvement of deep gray matter, hippocampal subfields, and ventricular changes in patients with amyotrophic lateral sclerosis (als). 2015-09-21 2023-08-13 human
Geidy E Serrano, Marwan N Sabbagh, Lucia I Sue, Jose A Hidalgo, Julie A Schneider, Barry J Bedell, Vivianna M Van Deerlin, Eunran Suh, Haruhiko Akiyama, Abhinay D Joshi, Michael J Pontecorvo, Mark A Mintun, Thomas G Beac. Positive florbetapir PET amyloid imaging in a subject with frequent cortical neuritic plaques and frontotemporal lobar degeneration with TDP43-positive inclusions. Journal of Alzheimer's disease : JAD. vol 42. issue 3. 2015-08-25. PMID:24927705. abnormal neuronal accumulation and modification of tar dna binding protein 43 (tdp-43) have recently been discovered to be defining histopathological features of particular subtypes of frontotemporal dementia and amyotrophic lateral sclerosis, and are also common in aging, particularly coexisting with hippocampal sclerosis and alzheimer's disease pathology. 2015-08-25 2023-08-13 human
. Correction: The Wobbler mouse model of amyotrophic lateral sclerosis (ALS) displays hippocampal hyperexcitability, and reduced number of interneurons, but no presynaptic vesicle release impairments. PloS one. vol 10. issue 3. 2015-07-27. PMID:25806789. correction: the wobbler mouse model of amyotrophic lateral sclerosis (als) displays hippocampal hyperexcitability, and reduced number of interneurons, but no presynaptic vesicle release impairments. 2015-07-27 2023-08-13 mouse
Lauren D Stutzbach, Sharon X Xie, Adam C Naj, Roger Albin, Sid Gilman, Virginia M Y Lee, John Q Trojanowski, Bernie Devlin, Gerard D Schellenber. The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease. Acta neuropathologica communications. vol 1. 2015-03-31. PMID:24252572. recently, several groups noted upr activation in alzheimer's disease (ad), parkinson's disease (pd), amyotrophic lateral sclerosis, multiple system atrophy, and in the hippocampus and substantia nigra of psp subjects. 2015-03-31 2023-08-12 human