| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Lore Wyers, Karen Verheyen, Berten Ceulemans, An-Sofie Schoonjans, Kaat Desloovere, Patricia Van de Walle, Ann Halleman. The mechanics behind gait problems in patients with Dravet Syndrome. Gait & posture. vol 84. 2021-07-16. PMID:33445141. |
dravet syndrome (ds) is a developmental and epileptic encephalopathy starting in infancy and characterised by treatment resistant epilepsy with cognitive impairment and progressive motor dysfunction. |
2021-07-16 |
2023-08-13 |
Not clear |
| Wesley T Kerr, Xingruo Zhang, Chloe E Hill, Emily A Janio, Andrea M Chau, Chelsea T Braesch, Justine M Le, Jessica M Hori, Akash B Patel, Corinne H Allas, Amir H Karimi, Ishita Dubey, Siddhika S Sreenivasan, Norma L Gallardo, Janar Bauirjan, Eric S Hwang, Emily C Davis, Shannon R D'Ambrosio, Mona Al Banna, Andrew Y Cho, Sandra R Dewar, Jerome Engel, Jamie D Feusner, John M Ster. Epilepsy, dissociative seizures, and mixed: Associations with time to video-EEG. Seizure. vol 86. 2021-07-12. PMID:33601302. |
video-electroencephalographic monitoring (vem) is a core component to the diagnosis and evaluation of epilepsy and dissociative seizures (ds)-also known as functional or psychogenic seizures-but vem evaluation often occurs later than recommended. |
2021-07-12 |
2023-08-13 |
Not clear |
| Miren Altuna, Sandra Giménez, Juan Forte. Epilepsy in Down Syndrome: A Highly Prevalent Comorbidity. Journal of clinical medicine. vol 10. issue 13. 2021-07-11. PMID:34202784. |
individuals with down syndrome (ds) have an increased risk for epilepsy during the whole lifespan, but especially after age 40 years. |
2021-07-11 |
2023-08-13 |
Not clear |
| Miren Altuna, Sandra Giménez, Juan Forte. Epilepsy in Down Syndrome: A Highly Prevalent Comorbidity. Journal of clinical medicine. vol 10. issue 13. 2021-07-11. PMID:34202784. |
the increase in the number of individuals with ds living into late middle age due to improved health care is resulting in an increase in epilepsy prevalence in this population. |
2021-07-11 |
2023-08-13 |
Not clear |
| Miren Altuna, Sandra Giménez, Juan Forte. Epilepsy in Down Syndrome: A Highly Prevalent Comorbidity. Journal of clinical medicine. vol 10. issue 13. 2021-07-11. PMID:34202784. |
this late onset epilepsy is linked to the development of symptomatic alzheimer's disease (ad), which is the main comorbidity in adults with ds with a cumulative incidence of more than 90% of adults by the seventh decade. |
2021-07-11 |
2023-08-13 |
Not clear |
| Miren Altuna, Sandra Giménez, Juan Forte. Epilepsy in Down Syndrome: A Highly Prevalent Comorbidity. Journal of clinical medicine. vol 10. issue 13. 2021-07-11. PMID:34202784. |
more than 50% of patients with ds and ad dementia will most likely develop epilepsy, which in this context has a specific clinical presentation in the form of generalized myoclonic epilepsy. |
2021-07-11 |
2023-08-13 |
Not clear |
| Miren Altuna, Sandra Giménez, Juan Forte. Epilepsy in Down Syndrome: A Highly Prevalent Comorbidity. Journal of clinical medicine. vol 10. issue 13. 2021-07-11. PMID:34202784. |
raised awareness and a better understanding of epilepsy in ds from families, caregivers and clinicians could enable earlier diagnoses and better treatments for individuals with ds. |
2021-07-11 |
2023-08-13 |
Not clear |
| Simona Lattanzi, Francesco Brigo, Eugen Trinka, Gaetano Zaccara, Pasquale Striano, Cinzia Del Giovane, Mauro Silvestrin. Adjunctive Cannabidiol in Patients with Dravet Syndrome: A Systematic Review and Meta-Analysis of Efficacy and Safety. CNS drugs. vol 34. issue 3. 2021-06-11. PMID:32040850. |
dravet syndrome (ds) is one of the most severe forms of drug-resistant epilepsy and available interventions fail to control seizures in most patients. |
2021-06-11 |
2023-08-13 |
Not clear |
| Piero Pavone, Xena Giada Pappalardo, Simona D Marino, Laura Sciuto, Giovanni Corsello, Martino Ruggieri, Enrico Parano, Maria Piccione, Raffaele Falsaperl. A novel GABRB3 variant in Dravet syndrome: Case report and literature review. Molecular genetics & genomic medicine. vol 8. issue 11. 2021-06-07. PMID:32945607. |
mutations in gabrb3 have been identified in subjects with different types of epilepsy and epileptic syndromes, including west syndrome (ws), dravet syndrome (ds), lennox-gastaut syndrome (lgs), myoclonic-atonic epilepsy (mae), and others. |
2021-06-07 |
2023-08-13 |
human |
| 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 |