Similar articles for PMID: 31444242

Year	Number of Results
1947	1
1948	3
1949	2
1989	2
2011	3
2012	8
2013	6
2014	10
2015	15
2016	15
2017	16
2018	9
2019	15
2020	6
2021	17
2022	11
2023	2
2024	0

1

Dravet syndrome and parkinsonism: A case report investigating the dopaminergic system.

Deuel L, Collins AE, Maa EH, Barr JP, Kern DS. Deuel L, et al. Neurology. 2019 Sep 24;93(13):595-596. doi: 10.1212/WNL.0000000000008171. Epub 2019 Aug 23. Neurology. 2019. PMID: 31444242 No abstract available.

2

A novel variant in SCN1A gene associated with Dravet syndrome.

Pathirana B, Hettiarachchi D, Neththikumara NF, Ratnayake PD, Dissanayake V. Pathirana B, et al. Seizure. 2019 Jul;69:213-214. doi: 10.1016/j.seizure.2019.05.003. Epub 2019 May 10. Seizure. 2019. PMID: 31102827 Free article. No abstract available.

3

Broadening Neurologic Manifestations in Adult Patients With Dravet Syndrome.

Tsuji S. Tsuji S. Neurology. 2022 May 31;98(22):913-914. doi: 10.1212/WNL.0000000000200753. Epub 2022 Apr 13. Neurology. 2022. PMID: 35418455 No abstract available.

4

Should we still consider Dravet syndrome an epileptic encephalopathy?

Auvin S. Auvin S. Epilepsy Behav. 2014 Jul;36:80-1. doi: 10.1016/j.yebeh.2014.05.010. Epub 2014 Jun 2. Epilepsy Behav. 2014. PMID: 24892752 No abstract available.

5

Outcomes and comorbidities of SCN1A-related seizure disorders.

de Lange IM, Gunning B, Sonsma ACM, van Gemert L, van Kempen M, Verbeek NE, Sinoo C, Nicolai J, Knoers NVAM, Koeleman BPC, Brilstra EH. de Lange IM, et al. Epilepsy Behav. 2019 Jan;90:252-259. doi: 10.1016/j.yebeh.2018.09.041. Epub 2018 Dec 5. Epilepsy Behav. 2019. PMID: 30527252 Free article.

6

Genetic therapeutic advancements for Dravet Syndrome.

Chilcott E, Díaz JA, Bertram C, Berti M, Karda R. Chilcott E, et al. Epilepsy Behav. 2022 Jul;132:108741. doi: 10.1016/j.yebeh.2022.108741. Epub 2022 May 30. Epilepsy Behav. 2022. PMID: 35653814 Free article. Review.

7

Adult motor phenotype differentiates Dravet syndrome from Lennox-Gastaut syndrome and links SCN1A to early onset parkinsonian features.

Aljaafari D, Fasano A, Nascimento FA, Lang AE, Andrade DM. Aljaafari D, et al. Epilepsia. 2017 Mar;58(3):e44-e48. doi: 10.1111/epi.13692. Epub 2017 Feb 10. Epilepsia. 2017. PMID: 28186331

8

Early-onset eyelid stereotypies are a frequent and distinctive feature in Dravet syndrome.

Sala-Coromina J, Raspall-Chaure M, Marcé-Grau A, de la Ossa AM, Macaya A. Sala-Coromina J, et al. Seizure. 2021 Nov;92:155-157. doi: 10.1016/j.seizure.2021.08.020. Epub 2021 Sep 7. Seizure. 2021. PMID: 34521063 Free article.

9

Behavior problems and health-related quality of life in Dravet syndrome.

Sinoo C, de Lange IM, Westers P, Gunning WB, Jongmans MJ, Brilstra EH. Sinoo C, et al. Epilepsy Behav. 2019 Jan;90:217-227. doi: 10.1016/j.yebeh.2018.11.029. Epub 2018 Dec 19. Epilepsy Behav. 2019. PMID: 30578097

10

[Dravet syndrome and mitochondrial disease, are they comorbid pathologies?].

Cantarin-Extremera V, Ruiz-Falco Rojas ML, Garcia-Fernandez M, Duat-Rodriguez A, Lopez-Marin L, Calleja-Gero ML. Cantarin-Extremera V, et al. Rev Neurol. 2014 Nov 1;59(9):429-31. Rev Neurol. 2014. PMID: 25342058 Free article. Spanish. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

122 results

Results by year