| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Keiko Usui, Kiyohito Terada, Naotaka Usui, Kazumi Matsuda, Akihiko Kondo, Takayasu Tottori, Jun Shinozaki, Takashi Nagamine, Yushi Inou. Working memory deficit in drug-resistant epilepsy with an amygdala lesion. Epilepsy & behavior case reports. vol 10. 2020-09-30. PMID:30094180. |
this study compared temporal lobe epilepsy (tle) patients with amygdala lesion (al) without hippocampal sclerosis (hs) (tle-al) with patients with tle and hs without al (tle-hs). |
2020-09-30 |
2023-08-13 |
Not clear |
| Jose Eduardo Peixoto-Santos, Luciana Estefani Drumond de Carvalho, Ludmyla Kandratavicius, Paula Rejane Beserra Diniz, Renata Caldo Scandiuzzi, Roland Coras, Ingmar Blümcke, Joao Alberto Assirati, Carlos Gilberto Carlotti, Caio Cesar Marconato Simoes Matias, Carlos Ernesto Garrido Salmon, Antonio Carlos Dos Santos, Tonicarlo R Velasco, Marcio Flavio D Moraes, Joao Pereira Leit. Manual Hippocampal Subfield Segmentation Using High-Field MRI: Impact of Different Subfields in Hippocampal Volume Loss of Temporal Lobe Epilepsy Patients. Frontiers in neurology. vol 9. 2020-09-30. PMID:30524352. |
manual hippocampal subfield segmentation using high-field mri: impact of different subfields in hippocampal volume loss of temporal lobe epilepsy patients. |
2020-09-30 |
2023-08-13 |
Not clear |
| Jose Eduardo Peixoto-Santos, Luciana Estefani Drumond de Carvalho, Ludmyla Kandratavicius, Paula Rejane Beserra Diniz, Renata Caldo Scandiuzzi, Roland Coras, Ingmar Blümcke, Joao Alberto Assirati, Carlos Gilberto Carlotti, Caio Cesar Marconato Simoes Matias, Carlos Ernesto Garrido Salmon, Antonio Carlos Dos Santos, Tonicarlo R Velasco, Marcio Flavio D Moraes, Joao Pereira Leit. Manual Hippocampal Subfield Segmentation Using High-Field MRI: Impact of Different Subfields in Hippocampal Volume Loss of Temporal Lobe Epilepsy Patients. Frontiers in neurology. vol 9. 2020-09-30. PMID:30524352. |
in patients with temporal lobe epilepsy (tle), presurgical magnetic resonance imaging (mri) often reveals hippocampal atrophy, while neuropathological assessment indicates the different types of hippocampal sclerosis (hs). |
2020-09-30 |
2023-08-13 |
Not clear |
| Xu Zhao, Zhi-Qiang Zhou, Ying Xiong, Xu Chen, Ke Xu, Juan Li, Ying Hu, Xiao-Long Peng, Wen-Zhen Zh. Reduced Interhemispheric White Matter Asymmetries in Medial Temporal Lobe Epilepsy With Hippocampal Sclerosis. Frontiers in neurology. vol 10. 2020-09-30. PMID:31068889. |
reduced interhemispheric white matter asymmetries in medial temporal lobe epilepsy with hippocampal sclerosis. |
2020-09-30 |
2023-08-13 |
Not clear |
| Keiko Hatano, Takahiro Shimizu, Hideyuki Matsumoto, Ichiro Suzuki, Hideji Hashid. Dreamy State, Delusions, Audiovisual Hallucinations, and Metamorphopsia in a Lesional Lateral Temporal Lobe Epilepsy Followed by Ipsilateral Hippocampal Sclerosis. Case reports in neurology. vol 11. issue 2. 2020-09-30. PMID:31543805. |
dreamy state, delusions, audiovisual hallucinations, and metamorphopsia in a lesional lateral temporal lobe epilepsy followed by ipsilateral hippocampal sclerosis. |
2020-09-30 |
2023-08-13 |
Not clear |
| Larissa Kraus, Florian Hetsch, Ulf C Schneider, Helena Radbruch, Martin Holtkamp, Jochen C Meier, Pawel Fidzinsk. Dimethylethanolamine Decreases Epileptiform Activity in Acute Human Hippocampal Slices Frontiers in molecular neuroscience. vol 12. 2020-09-30. PMID:31551707. |
dimethylethanolamine decreases epileptiform activity in acute human hippocampal slices temporal lobe epilepsy (tle) is the most common form of focal epilepsy with about 30% of patients developing pharmacoresistance. |
2020-09-30 |
2023-08-13 |
human |
| Dinesh Upadhya, Maheedhar Kodali, Daniel Gitai, Olagide W Castro, Gabriele Zanirati, Raghavendra Upadhya, Sahithi Attaluri, Eeshika Mitra, Bing Shuai, Bharathi Hattiangady, Ashok K Shett. A Model of Chronic Temporal Lobe Epilepsy Presenting Constantly Rhythmic and Robust Spontaneous Seizures, Co-morbidities and Hippocampal Neuropathology. Aging and disease. vol 10. issue 5. 2020-09-30. PMID:31595192. |
a model of chronic temporal lobe epilepsy presenting constantly rhythmic and robust spontaneous seizures, co-morbidities and hippocampal neuropathology. |
2020-09-30 |
2023-08-13 |
human |
| Haiyu Liu, Kurt R Stover, Nila Sivanenthiran, Jonathan Chow, Chloe Cheng, Yapeng Liu, Stellar Lim, Chiping Wu, Donald F Weaver, James H Eubanks, Hongmei Song, Liang Zhan. Impaired Spatial Learning and Memory in Middle-Aged Mice with Kindling-Induced Spontaneous Recurrent Seizures. Frontiers in pharmacology. vol 10. 2020-09-30. PMID:31611787. |
we postulate that the extended hippocampal kindling in middle-aged mice may help explore epileptogenic mechanisms and comorbidities potentially relevant to new-onset temporal lobe epilepsy in adult and aging patients. |
2020-09-30 |
2023-08-13 |
mouse |
| b' G\\xc3\\xbcnay G\\xc3\\xbcl, Demet Yandim Ku\\xc5\\x9fcu, Mesude \\xc3\\x96zerden, Melek Kandemir, Fulya Eren, Bekir Tu\\xc4\\x9fcu, Cahit Keskinkili\\xc3\\xa7, Nalan Kayrak, Dursun Kirba\\xc5\\x9. Cognitive Outcome after Surgery in Patients with Mesial Temporal Lobe Epilepsy. Noro psikiyatri arsivi. vol 54. issue 1. 2020-09-29. PMID:28566958.' |
the aim of the present study was to evaluate the neuropsychological outcomes of patients with medically intractable unilateral mesial temporal lobe epilepsy (mtle) due to hippocampal sclerosis (hs) treated either by anterior temporal lobectomy (atl) or selective amygdalohippocampectomy (sah). |
2020-09-29 |
2023-08-13 |
Not clear |
| Silvia Colnaghi, Giorgio Beltrami, Guy Poloni, Anna Pichiecchio, Stefano Bastianello, Carlo Andrea Galimberti, Maurizio Versin. Parahippocampal Involvement in Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis: A Proof of Concept from Memory-Guided Saccades. Frontiers in neurology. vol 8. 2020-09-29. PMID:29163352. |
parahippocampal involvement in mesial temporal lobe epilepsy with hippocampal sclerosis: a proof of concept from memory-guided saccades. |
2020-09-29 |
2023-08-13 |
Not clear |
| Silvia Colnaghi, Giorgio Beltrami, Guy Poloni, Anna Pichiecchio, Stefano Bastianello, Carlo Andrea Galimberti, Maurizio Versin. Parahippocampal Involvement in Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis: A Proof of Concept from Memory-Guided Saccades. Frontiers in neurology. vol 8. 2020-09-29. PMID:29163352. |
mesial temporal lobe epilepsy with hippocampal sclerosis (mtle-hs) may involve extrahippocampal areas of structural damage and dysfunction. |
2020-09-29 |
2023-08-13 |
Not clear |
| Olagide W Castro, Dinesh Upadhya, Maheedhar Kodali, Ashok K Shett. Resveratrol for Easing Status Epilepticus Induced Brain Injury, Inflammation, Epileptogenesis, and Cognitive and Memory Dysfunction-Are We There Yet? Frontiers in neurology. vol 8. 2020-09-29. PMID:29180982. |
in many instances, over a period, the initial precipitating injury caused by se leads to temporal lobe epilepsy (tle), typified by spontaneous recurrent seizures, cognitive, memory and mood impairments associated with chronic inflammation, reduced neurogenesis, abnormal synaptic reorganization, and multiple molecular changes in the hippocampus. |
2020-09-29 |
2023-08-13 |
Not clear |
| José J Jarero-Basulto, Yadira Gasca-Martínez, Martha C Rivera-Cervantes, Mónica E Ureña-Guerrero, Alfredo I Feria-Velasco, Carlos Beas-Zarat. Interactions Between Epilepsy and Plasticity. Pharmaceuticals (Basel, Switzerland). vol 11. issue 1. 2020-09-29. PMID:29414852. |
thus, in this review, we analysed some neuroplastic changes triggered in the hippocampus in response to seizure-induced neuronal damage and how these changes could lead to the establishment of temporal lobe epilepsy, the most common type of focal human epilepsy. |
2020-09-29 |
2023-08-13 |
human |
| Canan Güvenç, Patrick Dupont, Jan Van den Stock, Laura Seynaeve, Kathleen Porke, Eva Dries, Karen Van Bouwel, Johannes van Loon, Tom Theys, Karolien E Goffin, Wim Van Paessche. Correlation of neuropsychological and metabolic changes after epilepsy surgery in patients with left mesial temporal lobe epilepsy with hippocampal sclerosis. EJNMMI research. vol 8. issue 1. 2020-09-29. PMID:29651571. |
correlation of neuropsychological and metabolic changes after epilepsy surgery in patients with left mesial temporal lobe epilepsy with hippocampal sclerosis. |
2020-09-29 |
2023-08-13 |
Not clear |
| Steve C Danze. Contributions of Adult-Generated Granule Cells to Hippocampal Pathology in Temporal Lobe Epilepsy: A Neuronal Bestiary. Brain plasticity (Amsterdam, Netherlands). vol 3. issue 2. 2020-09-29. PMID:30151341. |
contributions of adult-generated granule cells to hippocampal pathology in temporal lobe epilepsy: a neuronal bestiary. |
2020-09-29 |
2023-08-13 |
Not clear |
| Steve C Danze. Contributions of Adult-Generated Granule Cells to Hippocampal Pathology in Temporal Lobe Epilepsy: A Neuronal Bestiary. Brain plasticity (Amsterdam, Netherlands). vol 3. issue 2. 2020-09-29. PMID:30151341. |
during the development of temporal lobe epilepsy, newly-generated hippocampal granule cells integrate abnormally into the brain. |
2020-09-29 |
2023-08-13 |
Not clear |
| Clarissa F Cavarsan, Jackeline Malheiros, Clement Hamani, Imad Najm, Luciene Covola. Is Mossy Fiber Sprouting a Potential Therapeutic Target for Epilepsy? Frontiers in neurology. vol 9. 2020-09-29. PMID:30555406. |
mesial temporal lobe epilepsy (mtle) caused by hippocampal sclerosis is one of the most frequent focal epilepsies in adults. |
2020-09-29 |
2023-08-13 |
Not clear |
| Clarissa F Cavarsan, Jackeline Malheiros, Clement Hamani, Imad Najm, Luciene Covola. Is Mossy Fiber Sprouting a Potential Therapeutic Target for Epilepsy? Frontiers in neurology. vol 9. 2020-09-29. PMID:30555406. |
in this review, we highlight the role of mossy fiber sprouting in seizure generation and hippocampal excitability and discuss the response of alternative treatment strategies in terms of mfs and spontaneous recurrent seizures in models of tle (temporal lobe epilepsy). |
2020-09-29 |
2023-08-13 |
Not clear |
| Camilo Espinosa-Jovel, Rafael Toledano, Adolfo Jiménez-Huete, Ángel Aledo-Serrano, Irene García-Morales, Pablo Campo, Antonio Gil-Nage. Olfactory function in focal epilepsies: Understanding mesial temporal lobe epilepsy beyond the hippocampus. Epilepsia open. vol 4. issue 3. 2020-09-29. PMID:31440730. |
olfactory function in focal epilepsies: understanding mesial temporal lobe epilepsy beyond the hippocampus. |
2020-09-29 |
2023-08-13 |
Not clear |
| Camilo Espinosa-Jovel, Rafael Toledano, Adolfo Jiménez-Huete, Ángel Aledo-Serrano, Irene García-Morales, Pablo Campo, Antonio Gil-Nage. Olfactory function in focal epilepsies: Understanding mesial temporal lobe epilepsy beyond the hippocampus. Epilepsia open. vol 4. issue 3. 2020-09-29. PMID:31440730. |
according to these data, we raised the hypothesis that in patients with mesial temporal lobe epilepsy associated with hippocampal sclerosis exists an interictal dysfunction of olfactory processing that could be more significant compared to patients with extra-hippocampal focal epilepsy and healthy controls. |
2020-09-29 |
2023-08-13 |
Not clear |