| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| Hao Deng, Wen Zheng, Zhi Son. The genetics and molecular biology of fever-associated seizures or epilepsy. Expert reviews in molecular medicine. vol 20. 2018-12-13. PMID:29661262. |
it is common in infants and children, and generally includes febrile seizures (fs), febrile seizures plus (fs+), dravet syndrome (ds) and genetic epilepsy with febrile seizures plus (gefsp). |
2018-12-13 |
2023-08-13 |
Not clear |
| Stéphane Auvin, Mohamed Jeljeli, Béatrice Desnous, Nadia Soussi-Yanicostas, Pascal Dournaud, Ghislaine Sterker. Altered vaccine-induced immunity in children with Dravet syndrome. Epilepsia. vol 59. issue 4. 2018-12-11. PMID:29512885. |
we provide new insight into immune mechanisms associated with ds that might guide research for the development of new immunotherapeutic agents in this epilepsy syndrome. |
2018-12-11 |
2023-08-13 |
Not clear |
| M Morimoto, S Shimakawa, T Hashimoto, T Kitaoka, S Kyotan. Marked efficacy of combined three-drug therapy (Sodium Valproate, Topiramate and Stiripentol) in a patient with Dravet syndrome. Journal of clinical pharmacy and therapeutics. vol 43. issue 4. 2018-10-15. PMID:29265387. |
dravet syndrome (ds) is an intractable epilepsy syndrome. |
2018-10-15 |
2023-08-13 |
Not clear |
| Anna Tagliabue, Cinzia Ferraris, Francesca Uggeri, Claudia Trentani, Simona Bertoli, Valentina de Giorgis, Pierangelo Veggiotti, Marina Ell. Short-term impact of a classical ketogenic diet on gut microbiota in GLUT1 Deficiency Syndrome: A 3-month prospective observational study. Clinical nutrition ESPEN. vol 17. 2018-06-18. PMID:28361745. |
the classical ketogenic diet (kd) is a high-fat, very low-carbohydrate normocaloric diet used for drug-resistant epilepsy and glucose transporter 1 deficiency syndrome (glut1 ds). |
2018-06-18 |
2023-08-13 |
Not clear |
| Joshua S Kaplan, Nephi Stella, William A Catterall, Ruth E Westenbroe. Cannabidiol attenuates seizures and social deficits in a mouse model of Dravet syndrome. Proceedings of the National Academy of Sciences of the United States of America. vol 114. issue 42. 2018-06-18. PMID:28973916. |
here we show that cannabidiol (cbd) effectively reduced seizures and autistic-like social deficits in a well-validated mouse genetic model of dravet syndrome (ds), a severe childhood epilepsy disorder caused by loss-of-function mutations in the brain voltage-gated sodium channel na |
2018-06-18 |
2023-08-13 |
mouse |
| An-Sofie Schoonjans, Fabienne Marchau, Bernard P Paelinck, Lieven Lagae, Arnold Gammaitoni, Milka Pringsheim, Martin G Keane, Berten Ceuleman. Cardiovascular safety of low-dose fenfluramine in Dravet syndrome: a review of its benefit-risk profile in a new patient population. Current medical research and opinion. vol 33. issue 10. 2018-03-19. PMID:28704161. |
dravet syndrome (ds) is a rare, treatment-resistant epilepsy syndrome for which current treatment regimens are often ineffective. |
2018-03-19 |
2023-08-13 |
Not clear |
| An-Sofie Schoonjans, Fabienne Marchau, Bernard P Paelinck, Lieven Lagae, Arnold Gammaitoni, Milka Pringsheim, Martin G Keane, Berten Ceuleman. Cardiovascular safety of low-dose fenfluramine in Dravet syndrome: a review of its benefit-risk profile in a new patient population. Current medical research and opinion. vol 33. issue 10. 2018-03-19. PMID:28704161. |
fenfluramine is currently in development for treatment of ds, based on reports in the 1980s and 1990s of its anti-epileptic activity in pediatric patients with intractable epilepsy. |
2018-03-19 |
2023-08-13 |
Not clear |
| A Schoonjans, B P Paelinck, F Marchau, B Gunning, A Gammaitoni, B S Galer, L Lagae, B Ceuleman. Low-dose fenfluramine significantly reduces seizure frequency in Dravet syndrome: a prospective study of a new cohort of patients. European journal of neurology. vol 24. issue 2. 2017-12-21. PMID:27790834. |
dravet syndrome (ds) is a severe, drug-resistant epilepsy. |
2017-12-21 |
2023-08-13 |
Not clear |
| Marina Trivisano, Nicola Pietrafusa, Vincenzo di Ciommo, Simona Cappelletti, Luca de Palma, Alessandra Terracciano, Enrico Bertini, Federico Vigevano, Nicola Specchi. PCDH19-related epilepsy and Dravet Syndrome: Face-off between two early-onset epilepsies with fever sensitivity. Epilepsy research. vol 125. 2017-12-18. PMID:27371789. |
aim of this study is to compare pcdh19-related epilepsy and dravet syndrome (ds) in order to find out differences between these two infantile epilepsies with fever sensitivity. |
2017-12-18 |
2023-08-13 |
Not clear |