| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Michael LoPresti, Ataru Igarashi, Yaoki Sonohara, Sally Bowditc. The emotional burden of caring for patients with Lennox-Gastaut syndrome, Dravet syndrome, and tuberous sclerosis complex-associated epilepsy: A qualitative study in Japan. Epilepsy & behavior : E&B. vol 158. 2024-07-19. PMID:39029305. |
lennox-gastaut syndrome (lgs) and dravet syndrome (ds) are rare, childhood-onset conditions associated with severe, treatment-resistant epilepsy and developmental issues, including motor and cognitive impairment. |
2024-07-19 |
2024-07-22 |
Not clear |
| Michael LoPresti, Ataru Igarashi, Yaoki Sonohara, Sally Bowditc. The emotional burden of caring for patients with Lennox-Gastaut syndrome, Dravet syndrome, and tuberous sclerosis complex-associated epilepsy: A qualitative study in Japan. Epilepsy & behavior : E&B. vol 158. 2024-07-19. PMID:39029305. |
this cross-sectional, interview-based study examined the qualitative impact of caring for patients with lgs, ds, and tsc-associated epilepsy on caregivers in japan, from the perspective of both caregivers and physicians. |
2024-07-19 |
2024-07-22 |
Not clear |
| Robert T Wechsler, David E Burdette, Barry E Gidal, Ann Hyslop, Patricia E McGoldrick, Elizabeth A Thiele, James Valerian. Consensus panel recommendations for the optimization of EPIDIOLEX® treatment for seizures associated with Lennox-Gastaut syndrome, Dravet syndrome, and tuberous sclerosis complex. Epilepsia open. 2024-07-15. PMID:39007525. |
to establish consensus recommendations for epidiolex treatment optimization in lgs, ds, and tsc, a panel of seven hcps with expertise in epilepsy was convened. |
2024-07-15 |
2024-07-18 |
Not clear |
| Sandra Solaz, Elena Cardenal-Muñoz, Alicia Muñoz, Simona Giorgi, Federico V Pallardó, Carlos Romá-Mateo, José Ángel Aiba. Navigating Dravet syndrome in Spain: A cross-sectional study of diagnosis, management, and care coordination. Epilepsia open. 2024-07-10. PMID:38984594. |
dravet syndrome (ds) is a rare form of refractory epilepsy that begins in the first year of life. |
2024-07-10 |
2024-07-12 |
Not clear |
| Rui Dong, Ruifeng Jin, Hongwei Zhang, Haiyan Zhang, Min Xue, Yue Li, Kaihui Zhang, Yuqiang Lv, Xiaoying Li, Yi Liu, Zhongtao Ga. Genotypic and phenotypic characteristics of sodium channel-associated epilepsy in Chinese population. Journal of human genetics. 2024-06-16. PMID:38880818. |
scn1a variant carriers predominantly presented with dravet syndrome (ds) and genetic epilepsy with febrile seizures plus (gefs + ), featuring a heightened sensitivity to fever-induced seizures. |
2024-06-16 |
2024-06-19 |
human |
| Nga N Tran, James Liu, Tyler Bullock, David Flower. Respiratory Syncytial Virus in a Child With Dravet Syndrome: A Case Report. Cureus. vol 16. issue 4. 2024-06-03. PMID:38826591. |
the objective of this case report is to describe and document a case of respiratory syncytial virus (rsv) in a pediatric patient with dravet syndrome (ds), also known as severe myoclonic epilepsy of infancy. |
2024-06-03 |
2024-06-05 |
Not clear |
| Lisa M Clayton, Bahar Azadi, Claire Eldred, Galia Wilson, Robert Robinson, Sanjay M Sisodiy. Feeding Difficulties and Gastrostomy in Dravet Syndrome: A UK-Wide Survey and 2-Center Experience. Neurology. Clinical practice. vol 14. issue 3. 2024-05-13. PMID:38737515. |
dravet syndrome (ds) is one of the most common monogenic epilepsies. |
2024-05-13 |
2024-05-27 |
Not clear |
| Osama Y Muthaffar, Ahmed K Bamaga, Anas S Alyazidi, Layan S Baaishrah, Hussain A Alkhalifah, Rafah B Hariri, Maya S Khider, Sereen A Alahmad. Efficacy and tolerability of perampanel in pediatric patients with Dravet syndrome. Translational pediatrics. vol 13. issue 4. 2024-05-08. PMID:38715666. |
in 1978, charlotte dravet first described a form of epilepsy termed dravet syndrome (ds). |
2024-05-08 |
2024-05-27 |
Not clear |
| Yingchun Xu, Deng Chen, Ling Li. Optimal dose of fenfluramine in adjuvant treatment of drug-resistant epilepsy: evidence from randomized controlled trials. Frontiers in neurology. vol 15. 2024-04-09. PMID:38590719. |
several clinical trials have suggested that fenfluramine (ffa) is effective for the treatment of epilepsy in dravet syndrome (ds) and lennox-gastaut syndrome (lgs). |
2024-04-09 |
2024-04-11 |
Not clear |
| Michael LoPresti, Ataru Igarashi, Yaoki Sonohara, Sally Bowditc. A quantitative cross-sectional study of the burden of caring for patients with Lennox-Gastaut syndrome, Dravet syndrome, and tuberous sclerosis complex-associated epilepsy in Japan. Epilepsy & behavior : E&B. vol 154. 2024-03-31. PMID:38555725. |
lennox-gastaut syndrome (lgs), dravet syndrome (ds), and tuberous sclerosis complex (tsc)-associated epilepsy are rare conditions associated with severe childhood-onset epilepsy. |
2024-03-31 |
2024-04-03 |
Not clear |
| Amber Postma, Crista A Minderhoud, Wim M Otte, Floor E Jansen, W B Gunning, Judith S Verhoeven, Marian J Jongmans, Janneke R Zinkstok, Eva H Brilstr. Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes. Epilepsy & behavior : E&B. vol 154. 2024-03-21. PMID:38513571. |
a pathogenic variant in scn1a can result in a spectrum of phenotypes, including dravet syndrome (ds) and genetic epilepsy with febrile seizures plus (gefs + ) syndrome. |
2024-03-21 |
2024-03-24 |
Not clear |
| Nicholas Aderinto, Gbolahan Olatunji, Emmanuel Kokori, Yusuf Ismaila Ajayi, Olumide Akinmoju, Abiola Samuel Ayedun, Oluwapelumi Ikeoluwa Ayoola, Noah Oluwaseun Aderint. The efficacy and safety of cannabidiol (CBD) in pediatric patients with Dravet Syndrome: a narrative review of clinical trials. European journal of medical research. vol 29. issue 1. 2024-03-19. PMID:38500226. |
dravet syndrome (ds) is a rare and severe form of childhood epilepsy that is often refractory to conventional antiepileptic drugs. |
2024-03-19 |
2024-03-21 |
Not clear |
| Declan Gallagher, Eduardo Pérez-Palma, Tobias Bruenger, Ismael Ghanty, Eva Brilstra, Berten Ceulemans, Nicole Chemaly, Iris de Lange, Christel Depienne, Renzo Guerrini, Davide Mei, Rikke S Møller, Rima Nabbout, Brigid M Regan, Amy L Schneider, Ingrid E Scheffer, An-Sofie Schoonjans, Joseph D Symonds, Sarah Weckhuysen, Sameer M Zuberi, Dennis Lal, Andreas Brunklau. Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsies. Epilepsia. 2024-02-27. PMID:38410936. |
scn1a variants are associated with epilepsy syndromes ranging from mild genetic epilepsy with febrile seizures plus (gefs+) to severe dravet syndrome (ds). |
2024-02-27 |
2024-03-02 |
Not clear |
| Andrew Whitfield, Emma Leighton, Heather Boagey, Maria Ot. Dual diagnosis of epilepsy and dissociative seizures: Prescription patterns, feasibility and safety of rationalising antiseizure medication. Epilepsy & behavior : E&B. vol 152. 2024-01-26. PMID:38277845. |
patients with a dual-diagnosis of epilepsy and dissociative seizures (ds) have received far less attention than those with single pathology. |
2024-01-26 |
2024-01-29 |
Not clear |
| Jingyi Tong, Tingting Ji, Ting Liu, Jiaqi Liu, Yibin Chen, Zongjun Li, Na Lu, Qifu L. Efficacy and safety of six new antiseizure medications for adjunctive treatment of focal epilepsy and epileptic syndrome: A systematic review and network meta-analysis. Epilepsy & behavior : E&B. vol 152. 2024-01-26. PMID:38277848. |
this study aimed to evaluate the efficacy and safety of six new antiseizure medications (asms) for adjunctive treatment in adult patients with focal epilepsy and adolescents with dravet syndrome (ds), lennox-gastaut syndrome (lgs), or tuberous sclerosis complex (tsc). |
2024-01-26 |
2024-01-29 |
Not clear |
| Hueng-Chuen Fan, Ming-Tao Yang, Lung-Chang Lin, Kuo-Liang Chiang, Chuan-Mu Che. Clinical and Genetic Features of Dravet Syndrome: A Prime Example of the Role of Precision Medicine in Genetic Epilepsy. International journal of molecular sciences. vol 25. issue 1. 2024-01-11. PMID:38203200. |
dravet syndrome (ds), also known as severe myoclonic epilepsy of infancy, is a rare and drug-resistant form of developmental and epileptic encephalopathies, which is both debilitating and challenging to manage, typically arising during the first year of life, with seizures often triggered by fever, infections, or vaccinations. |
2024-01-11 |
2024-01-13 |
Not clear |
| Clarissa Corniello, Fedele Dono, Giacomo Evangelista, Astrid Thomas, Marco Onofrj, Stefano L Sens. Diagnosis and treatment of status epilepticus in Down Syndrome (DS): A case report and systematic literature review. Seizure. vol 114. 2023-12-15. PMID:38101201. |
epilepsy is one of the most frequent neurological comorbidities in patients with down syndrome (ds). |
2023-12-15 |
2023-12-18 |
Not clear |
| Nguyen Hong Nhu Y Trinh, Amy Susan Reid, Barbara Robertso. Perioperative considerations for adult patients with Dravet syndrome in regional centres. BMJ case reports. vol 16. issue 12. 2023-12-06. PMID:38056933. |
dravet syndrome (ds) is a rare and intractable severe form of epilepsy presenting in infancy with frequent prolonged myoclonic seizures and neurodevelopmental impairment, associated with a |
2023-12-06 |
2023-12-10 |
Not clear |
| Carla Ballesteros-Sayas, Alicia Muñoz-Montero, Simona Giorgi, Elena Cardenal-Muñoz, Eulalia Turón-Viñas, Federico Pallardó, José Ángel Aiba. Non-pharmacological therapeutic needs in people with Dravet syndrome. Epilepsy & behavior : E&B. vol 150. 2023-11-30. PMID:38035538. |
ds is characterised by a drug-resistant epilepsy and by cognitive and behavioural disturbances. |
2023-11-30 |
2023-12-10 |
Not clear |
| P Whyte-Fagundes, A Vance, A Carroll, F Figueroa, C Manukyan, S C Baraba. Testing of putative antiseizure drugs in a preclinical Dravet syndrome zebrafish model. bioRxiv : the preprint server for biology. 2023-11-28. PMID:38014342. |
dravet syndrome (ds) is a severe genetic epilepsy primarily caused by |
2023-11-28 |
2023-11-29 |
zebrafish |