| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| Soraya Martín-Suárez, Oihane Abiega, Ana Ricobaraza, Rubén Hernandez-Alcoceba, Juan Manuel Encina. Alterations of the Hippocampal Neurogenic Niche in a Mouse Model of Dravet Syndrome. Frontiers in cell and developmental biology. vol 8. 2020-09-28. PMID:32793597. |
we here analyze for the first time the alterations of the neurogenic niche in a novel mouse model of dravet syndrome (ds), a genetic encephalopathy with severe epilepsy in infancy and multiple neurological comorbidities. |
2020-09-28 |
2023-08-13 |
mouse |
| Daniel J Kats, Katherine J Roche, Brian G Skotk. Epileptic spasms in individuals with Down syndrome: A review of the current literature. Epilepsia open. vol 5. issue 3. 2020-09-28. PMID:32913943. |
epilepsy can occur in individuals with down syndrome (ds), with epileptic spasms representing the most frequent seizure type in this population. |
2020-09-28 |
2023-08-13 |
Not clear |
| Daniel J Kats, Katherine J Roche, Brian G Skotk. Epileptic spasms in individuals with Down syndrome: A review of the current literature. Epilepsia open. vol 5. issue 3. 2020-09-28. PMID:32913943. |
according to available literature, the global clinic-based lifetime prevalence of epilepsy in individuals with ds ranged from 1.6% to 23.1%, with epileptic spasms representing 6.7%-66.7% of these cases. |
2020-09-28 |
2023-08-13 |
Not clear |
| Daniel J Kats, Katherine J Roche, Brian G Skotk. Epileptic spasms in individuals with Down syndrome: A review of the current literature. Epilepsia open. vol 5. issue 3. 2020-09-28. PMID:32913943. |
generally, children with ds and epileptic spasms tend to be more responsive to treatment and have better outcomes than children with epileptic spasms of unknown etiology (ie, without ds), in terms of response and relapse rates as well as the development of intractable epilepsy (eg, lennox-gastaut syndrome). |
2020-09-28 |
2023-08-13 |
Not clear |
| Jens Schuster, Loora Laan, Joakim Klar, Zhe Jin, Mikael Huss, Sergiy Korol, Feria Hikmet Noraddin, Maria Sobol, Bryndis Birnir, Niklas Dah. Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulated pathways for chromatin remodeling and neurodevelopment. Neurobiology of disease. vol 132. 2020-08-06. PMID:31445158. |
dravet syndrome (ds) is an early onset refractory epilepsy typically caused by de novo heterozygous variants in scn1a encoding the α-subunit of the neuronal sodium channel na |
2020-08-06 |
2023-08-13 |
Not clear |
| Christine S Cheah, Brian N Lundstrom, William A Catterall, John C Oakle. Impairment of Sharp-Wave Ripples in a Murine Model of Dravet Syndrome. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 39. issue 46. 2020-06-30. PMID:31537705. |
dravet syndrome (ds) is a severe early-onset epilepsy associated with heterozygous loss-of-function mutations in |
2020-06-30 |
2023-08-13 |
Not clear |
| Masaya Katagiri, Koji Iida, Kumatoshi Ishihara, Dileep Nair, Kana Harada, Kota Kagawa, Go Seyama, Akira Hashizume, Takashi Kuramoto, Ryosuke Hanaya, Kazunori Arita, Kaoru Kuris. Anti-seizure effect and neuronal activity change in the genetic-epileptic model rat with acute and chronic vagus nerve stimulation. Epilepsy research. vol 155. 2020-05-26. PMID:31277035. |
noda epileptic rat (ner) is genetic epilepsy model rat which exhibits spontaneous generalized tonic-clonic seizure (gtc) approximately once per 30 h and frequent dialeptic seizure (ds). |
2020-05-26 |
2023-08-13 |
rat |
| Sara K Trowbridge, Christopher J Yuskaitis, Nicole Baumer, Mark Libenson, Sanjay P Prabhu, Chellamani Harin. Brain MRI abnormalities in patients with infantile spasms and Down syndrome. Epilepsy & behavior : E&B. vol 92. 2020-05-25. PMID:30616066. |
infantile spasms (is) are the most frequent epilepsy syndrome in children with down syndrome (ds). |
2020-05-25 |
2023-08-13 |
Not clear |
| Raymond E A Sanchez, Ivana L Bussi, Miriam Ben-Hamo, Carlos S Caldart, William A Catterall, Horacio O De La Iglesi. Circadian regulation of sleep in a pre-clinical model of Dravet syndrome: dynamics of sleep stage and siesta re-entrainment. Sleep. vol 42. issue 12. 2020-05-11. PMID:31346614. |
dravet syndrome (ds) is an intractable epilepsy accompanied by disturbed sleep. |
2020-05-11 |
2023-08-13 |
mouse |
| Jens Schuster, Ambrin Fatima, Maria Sobol, Feria Hikmet Norradin, Loora Laan, Niklas Dah. Generation of three human induced pluripotent stem cell (iPSC) lines from three patients with Dravet syndrome carrying distinct SCN1A gene mutations. Stem cell research. vol 39. 2020-04-27. PMID:31400703. |
dravet syndrome (ds) is a childhood epilepsy syndrome caused by heterozygous mutations in the scn1a gene encoding voltage-gated sodium channel na |
2020-04-27 |
2023-08-13 |
human |
| Francesca Darra, Domenica Battaglia, Charlotte Dravet, Mara Patrini, Francesca Offredi, Daniela Chieffo, Elena Piazza, Elena Fontana, Giorgia Olivieri, Ida Turrini, Bernardo Dalla Bernardina, Tiziana Granata, Francesca Ragon. Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults. Epilepsia. vol 60 Suppl 3. 2020-04-23. PMID:31904122. |
the study confirms that the global outcome of ds is poor in most cases, albeit epilepsy severity decreases throughout adulthood. |
2020-04-23 |
2023-08-13 |
Not clear |