| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Vaishali Satpute Janve, Lyndsey L Anderson, Dilara Bahceci, Nicole A Hawkins, Jennifer A Kearney, Jonathon C Arnol. The Heat Sensing Trpv1 Receptor Is Not a Viable Anticonvulsant Drug Target in the Frontiers in pharmacology. vol 12. 2021-06-05. PMID:34079465. |
the heat sensing trpv1 receptor is not a viable anticonvulsant drug target in the cannabidiol has been approved for the treatment of drug-resistant childhood epilepsies including dravet syndrome (ds). |
2021-06-05 |
2023-08-13 |
Not clear |
| Tommaso Lo Barco, Nicole Chemaly, Theo Teng, Francesca Darra, Rima Nabbou. Head circumferences of patients with Dravet syndrome show growth slowdown. Epilepsy & behavior : E&B. vol 111. 2021-03-16. PMID:32702652. |
to investigate the head growth trajectories in a pediatric population with ds, a retrospective analysis of medical records of patients with ds was performed in 2 epilepsy centers. |
2021-03-16 |
2023-08-13 |
human |
| Aline Kortas, Katharina Schiller, Gabriele Unterholzner, Markus Rauchenzaune. Accuracy of Flash Glucose Monitoring in a Patient with Dravet Syndrome on a Ketogenic Diet. Neuropediatrics. vol 51. issue 1. 2021-02-05. PMID:31529424. |
we herein report the case of a 3-year-old girl with severe myoclonic epilepsy of infancy known as dravet syndrome (ds) on a ketogenic diet (kd) whose glucose concentrations were controlled by using a flash glucose monitoring system. |
2021-02-05 |
2023-08-13 |
Not clear |
| Debopam Samant. Changing Landscape of Dravet Syndrome Management: An Overview. Neuropediatrics. vol 51. issue 2. 2021-02-05. PMID:32079034. |
dravet syndrome (ds), previously known as severe myoclonic epilepsy of infancy, is a severe developmental and epileptic encephalopathy caused by loss-of-function mutations in one copy of |
2021-02-05 |
2023-08-13 |
Not clear |
| Nicola Specchio, Nicola Pietrafusa, Viola Doccini, Marina Trivisano, Francesca Darra, Francesca Ragona, Alberto Cossu, Silvia Spolverato, Domenica Battaglia, Michela Quintiliani, Maria Luigia Gambardella, Anna Rosati, Davide Mei, Tiziana Granata, Bernardo Dalla Bernardina, Federico Vigevano, Renzo Guerrin. Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study. Epilepsia. vol 61. issue 11. 2021-02-03. PMID:32945537. |
dravet syndrome (ds) is a drug-resistant, infantile onset epilepsy syndrome with multiple seizure types and developmental delay. |
2021-02-03 |
2023-08-13 |
Not clear |
| Danielle M Boyce, Orrin Devinsky, Mary Anne Meski. Barriers to transition from pediatric to adult care for patients with Dravet syndrome: A focus group study of caregivers. Epilepsy & behavior : E&B. vol 109. 2021-02-01. PMID:32422576. |
caregivers of individuals with intellectual and developmental disabilities and epilepsy such as dravet syndrome (ds) must navigate a complex web of state and community services through the transition from child-centered to adult-oriented healthcare. |
2021-02-01 |
2023-08-13 |
human |
| Alex J Berry, Macide Yuksel, Barnaby J Proctor, Jacqueline Foon. Cognitive behavior therapy for comorbid dissociative seizures in patients with epilepsy. Epilepsy & behavior : E&B. vol 106. 2021-01-19. PMID:32169599. |
the main aim of this study was to assess the effectiveness of cognitive behavior therapy (cbt) for comorbid dissociative seizures (ds) in patients with epilepsy. |
2021-01-19 |
2023-08-13 |
Not clear |
| Mario Tombini, Giovanni Assenza, Livia Quintiliani, Lorenzo Ricci, Jacopo Lanzone, Martina Ulivi, Vincenzo Di Lazzar. Depressive symptoms and difficulties in emotion regulation in adult patients with epilepsy: Association with quality of life and stigma. Epilepsy & behavior : E&B. vol 107. 2021-01-18. PMID:32320931. |
the objective of the study was to assess depressive symptoms (ds) and difficulties in emotion regulation (er) in adult people with epilepsy (pwe) and their correlation with quality of life and stigmatization feelings of patients. |
2021-01-18 |
2023-08-13 |
Not clear |
| Ágnes Till, Judith Zima, Anett Fekete, Judit Bene, Márta Czakó, András Szabó, Béla Melegh, Kinga Hadzsie. Mutation spectrum of the SCN1A gene in a Hungarian population with epilepsy. Seizure. vol 74. 2020-11-16. PMID:31765958. |
the vast majority of mutations responsible for epilepsy syndromes such as genetic epilepsy with febrile seizures plus (gefs+) and dravet syndrome (ds) occur in the gene encoding the type 1 alpha subunit of neuronal voltage-gated sodium channel (scn1a). |
2020-11-16 |
2023-08-13 |
Not clear |
| Yukun Yuan, Heather A O'Malley, Melissa A Smaldino, Alexandra A Bouza, Jacob M Hull, Lori L Iso. Delayed maturation of GABAergic signaling in the Scn1a and Scn1b mouse models of Dravet Syndrome. Scientific reports. vol 9. issue 1. 2020-11-03. PMID:30996233. |
dravet syndrome (ds) is a catastrophic developmental and epileptic encephalopathy characterized by severe, pharmacoresistant seizures and the highest risk of sudden unexpected death in epilepsy (sudep) of all epilepsy syndromes. |
2020-11-03 |
2023-08-13 |
mouse |
| Rima Nabbout, Elizabeth A Thiel. The role of cannabinoids in epilepsy treatment: a critical review of efficacy results from clinical trials. Epileptic disorders : international epilepsy journal with videotape. vol 22. issue S1. 2020-11-02. PMID:31916540. |
results of these trials led to the fda and ema approval respectively in 2018 and 2019 for the treatment of seizures associated with two rare epilepsies: lennox-gastaut syndrome (lgs) or dravet syndrome (ds) in patients two years of age and older. |
2020-11-02 |
2023-08-13 |
Not clear |
| Paul G Hatini, Kathryn G Common. Serotonin abnormalities in Dravet syndrome mice before and after the age of seizure onset. Brain research. vol 1724. 2020-10-29. PMID:31445030. |
dravet syndrome (ds) is a genetic form of severe epilepsy often associated with mutation of the scn1a gene encoding the voltage gated sodium channel nav1.1. |
2020-10-29 |
2023-08-13 |
mouse |
| Ana Ricobaraza, Lucia Mora-Jimenez, Elena Puerta, Rocio Sanchez-Carpintero, Ana Mingorance, Julio Artieda, Maria Jesus Nicolas, Guillermo Besne, Maria Bunuales, Manuela Gonzalez-Aparicio, Noemi Sola-Sevilla, Miguel Valencia, Ruben Hernandez-Alcoceb. Epilepsy and neuropsychiatric comorbidities in mice carrying a recurrent Dravet syndrome SCN1A missense mutation. Scientific reports. vol 9. issue 1. 2020-10-28. PMID:31578435. |
dravet syndrome (ds) is an encephalopathy with epilepsy associated with multiple neuropsychiatric comorbidities. |
2020-10-28 |
2023-08-13 |
mouse |
| Mahmut Aslan, Bilge Ozgor, Serkan Kirik, Serdal Gungo. A Novel Journal of pediatric neurosciences. vol 15. issue 2. 2020-10-13. PMID:33042244. |
a novel dravet syndrome (ds) is characterized by severe infant-onset myoclonic epilepsy with delayed psychomotor development and increased premature mortality. |
2020-10-13 |
2023-08-13 |
Not clear |
| Arsalan Anwar, Sidra Saleem, Urvish K Patel, Kogulavadanan Arumaithurai, Preeti Mali. Dravet Syndrome: An Overview. Cureus. vol 11. issue 6. 2020-10-01. PMID:31497436. |
dravet syndrome (ds), also known as severe myoclonic epilepsy of infancy (smei), is one of the rare early childhood intractable epileptic encephalopathies associated with pleomorphic seizure activity, cognitive decline, motor, and behavioral abnormalities. |
2020-10-01 |
2023-08-13 |
Not clear |
| Arsalan Anwar, Sidra Saleem, Urvish K Patel, Kogulavadanan Arumaithurai, Preeti Mali. Dravet Syndrome: An Overview. Cureus. vol 11. issue 6. 2020-10-01. PMID:31497436. |
due to drug-refractory epilepsy in ds, many more therapies are being investigated to increase the longevity of patients. |
2020-10-01 |
2023-08-13 |
Not clear |
| b' Anna-Marieta Moise, Linda Leary, Lola C Morgan, Alex M Papanastassiou, C \\xc3\\x81kos Szab\\xc3\\xb. Ictal laughter and crying: Should they be classified as automatisms? Epilepsy & behavior case reports. vol 7. 2020-09-30. PMID:28239548.' |
dacrystic seizures (ds), characterized by ictal crying, also have been reported in hypothalamic lesions and focal epilepsy. |
2020-09-30 |
2023-08-13 |
Not clear |
| Carlos G Aguirre-Velázque. Report from a Survey of Parents Regarding the Use of Cannabidiol Neurology research international. vol 2017. 2020-09-30. PMID:28392943. |
of the 43 mexican cases, the diagnoses were as follows: 20 cases (47%) had lennox-gastaut syndrome (lgs); 13 cases (30%) had unspecified refractory epilepsy (ure); 8 cases (19%) had west syndrome (ws); 1 case (2%) had doose syndrome (ds); and 1 case (2%) had ohtahara syndrome (os). |
2020-09-30 |
2023-08-13 |
Not clear |
| Frida A Teran, YuJaung Kim, Megan S Crotts, Eduardo Bravo, Katlynn J Emaus, George B Richerso. Time of Day and a Ketogenic Diet Influence Susceptibility to SUDEP in Frontiers in neurology. vol 10. 2020-09-29. PMID:30984098. |
dravet syndrome (ds) is a severe childhood-onset epilepsy commonly caused by mutations in the |
2020-09-29 |
2023-08-13 |
Not clear |
| Shenhai Liu, Zhe Jin, Yiling Zhang, ShiKuo Rong, Wenxin He, Kuisheng Sun, Din Wan, Junming Huo, Lifei Xiao, Xinxiao Li, Na Ding, Feng Wang, Tao Su. The Glucagon-Like Peptide-1 Analogue Liraglutide Reduces Seizures Susceptibility, Cognition Dysfunction and Neuronal Apoptosis in a Mouse Model of Dravet Syndrome. Frontiers in pharmacology. vol 11. 2020-09-28. PMID:32184723. |
dravet syndrome (ds) is a refractory epilepsy typically caused by heterozygous mutations of the |
2020-09-28 |
2023-08-13 |
mouse |