| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Adam Strzelczyk, Susanne Schubert-Bast, Thomas Bast, Ulrich Bettendorf, Barbara Fiedler, Hajo M Hamer, Arne Herting, Malin Kalski, Lara Kay, Matthias Kieslich, Karl Martin Klein, Gerhard Kluger, Gerhard Kurlemann, Thomas Mayer, Bernd A Neubauer, Tilman Polster, Sarah von Spiczak, Ulrich Stephani, Regina Trollmann, Adelheid Wiemer-Kruel, Markus Wolff, John Irwin, Joe Carroll, Clive Pritchard, Felix Roseno. A multicenter, matched case-control analysis comparing burden-of-illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany. Epilepsia. vol 60. issue 8. 2020-04-15. PMID:31247127. |
to compare direct and indirect costs and quality of life (qol) of pediatric and adult patients with dravet syndrome (ds), with drug-resistant epilepsy (dre) and in seizure remission (sr), and their caregivers, in germany. |
2020-04-15 |
2023-08-13 |
Not clear |
| Fu-Shan Kuo, Colin M Cleary, Joseph J LoTurco, Xinnian Chen, Daniel K Mulke. Disordered breathing in a mouse model of Dravet syndrome. eLife. vol 8. 2020-02-24. PMID:31025941. |
dravet syndrome (ds) is a form of epilepsy with a high incidence of sudden unexpected death in epilepsy (sudep). |
2020-02-24 |
2023-08-13 |
mouse |
| Naohiro Ohshita, Kaname Tsuji, Hiroaki Yoshida, Hiroki Shibata, Yoshiko Matsuda, Yasuo M Tsutsumi, Yoshihiro Momot. Anesthetic Management of Patient With Dravet Syndrome: A Case Report. Anesthesia progress. vol 66. issue 3. 2020-02-17. PMID:31545672. |
dravet syndrome (ds) is a rare and severe form of epilepsy that begins in infancy. |
2020-02-17 |
2023-08-13 |
Not clear |
| Zhigang Liu, Xingguang Ye, Peixiu Qiao, Weiyao Luo, Yanling Wu, Yun He, Pingming Ga. G327E mutation in SCN9A gene causes idiopathic focal epilepsy with Rolandic spikes: a case report of twin sisters. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 40. issue 7. 2020-01-13. PMID:30834459. |
phenotypes of scn9a mutations include febrile seizures (fs), genetic epilepsy with febrile seizures plus (gefs+), and dravet syndrome (ds), which pose challenges in clinical treatment. |
2020-01-13 |
2023-08-13 |
Not clear |
| M M Rahman, K Fatem. Seizures in Down Syndrome: An Update. Mymensingh medical journal : MMJ. vol 28. issue 3. 2019-10-21. PMID:31391451. |
rates of epilepsy in ds range from 1-13%. |
2019-10-21 |
2023-08-13 |
Not clear |
| M M Rahman, K Fatem. Seizures in Down Syndrome: An Update. Mymensingh medical journal : MMJ. vol 28. issue 3. 2019-10-21. PMID:31391451. |
sex distribution for epilepsy in children with ds varies. |
2019-10-21 |
2023-08-13 |
Not clear |
| M M Rahman, K Fatem. Seizures in Down Syndrome: An Update. Mymensingh medical journal : MMJ. vol 28. issue 3. 2019-10-21. PMID:31391451. |
the pharmacological treatment of epilepsy in ds is same as that of other patients diagnosed with epilepsy. |
2019-10-21 |
2023-08-13 |
Not clear |
| M M Rahman, K Fatem. Seizures in Down Syndrome: An Update. Mymensingh medical journal : MMJ. vol 28. issue 3. 2019-10-21. PMID:31391451. |
the diagnosis, classification and treatment of epilepsy in ds follow the guidelines applied to the general population. |
2019-10-21 |
2023-08-13 |
Not clear |
| M M Rahman, K Fatem. Seizures in Down Syndrome: An Update. Mymensingh medical journal : MMJ. vol 28. issue 3. 2019-10-21. PMID:31391451. |
review of literatures from 1960 to 2017 and electronically identified articles on epilepsy in down syndrome in children in english are searched from internet and pub med to describe features of seizures in children with ds. |
2019-10-21 |
2023-08-13 |
Not clear |
| Gustavo Wandresen, Fernanda Sgarbi, Renato Nisihar. Management of contraceptives and menstrual complaints in patients with Down syndrome. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology. vol 35. issue 2. 2019-08-12. PMID:30324830. |
however, individuals with ds may have a higher incidence of other disorders related to menstruation, such as hypothyroidism, epilepsy and use of anticonvulsants. |
2019-08-12 |
2023-08-13 |
Not clear |
| Federica Lotti, Ursula Geronzi, Salvatore Gross. Electroencephalographic and epilepsy findings in mecp2 duplication syndrome. A family study. Brain & development. vol 41. issue 5. 2019-07-26. PMID:30642617. |
mecp2 duplication syndrome (mecp2 ds) is an x-linked disorder characterized by early-onset hypotonia, poor speech development, recurrent respiratory infections, epilepsy and progressive spasticity. |
2019-07-26 |
2023-08-13 |
Not clear |
| YuJaung Kim, Eduardo Bravo, Caitlin K Thirnbeck, Lori A Smith-Mellecker, Se Hee Kim, Brian K Gehlbach, Linda C Laux, Xiuqiong Zhou, Douglas R Nordli, George B Richerso. Severe peri-ictal respiratory dysfunction is common in Dravet syndrome. The Journal of clinical investigation. vol 128. issue 3. 2019-07-15. PMID:29329111. |
dravet syndrome (ds) is a severe childhood-onset epilepsy commonly due to mutations of the sodium channel gene scn1a. |
2019-07-15 |
2023-08-13 |
mouse |
| YuJaung Kim, Eduardo Bravo, Caitlin K Thirnbeck, Lori A Smith-Mellecker, Se Hee Kim, Brian K Gehlbach, Linda C Laux, Xiuqiong Zhou, Douglas R Nordli, George B Richerso. Severe peri-ictal respiratory dysfunction is common in Dravet syndrome. The Journal of clinical investigation. vol 128. issue 3. 2019-07-15. PMID:29329111. |
patients with ds have a high risk of sudden unexplained death in epilepsy (sudep), widely believed to be due to cardiac mechanisms. |
2019-07-15 |
2023-08-13 |
mouse |
| Claudia Sinoo, Iris Marie-Louise de Lange, Paul Westers, Willem Boudewijn Gunning, Marian Jacqueline Jongmans, Eva Henriëtte Brilstr. Behavior problems and health-related quality of life in Dravet syndrome. Epilepsy & behavior : E&B. vol 90. 2019-07-09. PMID:30578097. |
the current study aimed to give more insight into (1) the prevalence of a wide range of specific behavior difficulties and aspects of health-related quality of life (hrqol) in patients with ds compared with the general population (gp) and patients with epilepsy without ds, (2) the relations between these behavior problems and different aspects of hrqol, and (3) the associations between seizure frequency, cognitive impairment (ci), behavior problems, and hrqol, based on a conceptual model. |
2019-07-09 |
2023-08-13 |
Not clear |
| Dilsad Turkdogan, Gulten Thomas, Birsen Demire. Ketogenic diet as a successful early treatment modality for SCN2A mutation. Brain & development. vol 41. issue 4. 2019-06-17. PMID:30415926. |
scn2a mutations have been described in a very broad spectrum of clinical phenotypes including benign (familial) neonatal/infantile seizures and early infantile epileptic encephalopathies (eiee) as ohtahara syndrome (os), dravet syndrome (ds), epilepsy of infancy with migrating focal seizures and west syndrome (ws). |
2019-06-17 |
2023-08-13 |
Not clear |
| Kelly G Knupp, Elaine C Wirrel. Treatment Strategies for Dravet Syndrome. CNS drugs. vol 32. issue 4. 2019-05-30. PMID:29594870. |
dravet syndrome (ds) is a medically refractory epilepsy that onsets in the first year of life with prolonged seizures, often triggered by fever. |
2019-05-30 |
2023-08-13 |
Not clear |
| S Lattanzi, E Trinka, E Russo, P Striano, R Citraro, M Silvestrini, F Brig. Cannabidiol as adjunctive treatment of seizures associated with Lennox-Gastaut syndrome and Dravet syndrome. Drugs of today (Barcelona, Spain : 1998). vol 55. issue 3. 2019-05-20. PMID:30938373. |
lennox-gastaut syndrome (lgs) and dravet syndrome (ds) are severe, refractory epilepsy syndromes with onset in early childhood. |
2019-05-20 |
2023-08-13 |
human |
| Benjamin Andreas Berk, Rowena Mary Anne Packer, Tsz Hong Law, Holger Andreas Vol. Investigating owner use of dietary supplements in dogs with idiopathic epilepsy. Research in veterinary science. vol 119. 2019-04-30. PMID:30064067. |
some diets have been shown to have a positive impact upon the seizure activity in dogs with idiopathic epilepsy (ie), while other diets and dietary supplements (ds), although marketed as providing health benefits, lack conclusive scientific evidence on their actual beneficial effects. |
2019-04-30 |
2023-08-13 |
dog |
| Benjamin Andreas Berk, Rowena Mary Anne Packer, Tsz Hong Law, Holger Andreas Vol. Investigating owner use of dietary supplements in dogs with idiopathic epilepsy. Research in veterinary science. vol 119. 2019-04-30. PMID:30064067. |
we propose that use of ds should be considered and monitored by veterinary surgeons in epilepsy management. |
2019-04-30 |
2023-08-13 |
dog |
| An-Sofie Schoonjans, Shauni De Keersmaecker, Maxime Van Bouwel, Berten Ceuleman. More daytime sleepiness and worse quality of sleep in patients with Dravet Syndrome compared to other epilepsy patients. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. vol 23. issue 1. 2019-02-27. PMID:30340858. |
in this study we explored the sleep behavior in ds and compared the prevalence of sleep problems with other epilepsy patients. |
2019-02-27 |
2023-08-13 |
Not clear |