168 related articles for article (PubMed ID: 34002542)
1. Loss-of-function variants in K
Soh MS; Bagnall RD; Bennett MF; Bleakley LE; Mohamed Syazwan ES; Phillips AM; Chiam MDF; McKenzie CE; Hildebrand M; Crompton D; Bahlo M; Semsarian C; Scheffer IE; Berkovic SF; Reid CA
Ann Clin Transl Neurol; 2021 Jul; 8(7):1422-1432. PubMed ID: 34002542
[TBL] [Abstract][Full Text] [Related]
2. Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases.
Tu E; Bagnall RD; Duflou J; Semsarian C
Brain Pathol; 2011 Mar; 21(2):201-8. PubMed ID: 20875080
[TBL] [Abstract][Full Text] [Related]
3. Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy.
Bagnall RD; Crompton DE; Petrovski S; Lam L; Cutmore C; Garry SI; Sadleir LG; Dibbens LM; Cairns A; Kivity S; Afawi Z; Regan BM; Duflou J; Berkovic SF; Scheffer IE; Semsarian C
Ann Neurol; 2016 Apr; 79(4):522-34. PubMed ID: 26704558
[TBL] [Abstract][Full Text] [Related]
4. Systematic Review of the Genetics of Sudden Unexpected Death in Epilepsy: Potential Overlap With Sudden Cardiac Death and Arrhythmia-Related Genes.
Chahal CAA; Salloum MN; Alahdab F; Gottwald JA; Tester DJ; Anwer LA; So EL; Murad MH; St Louis EK; Ackerman MJ; Somers VK
J Am Heart Assoc; 2020 Jan; 9(1):e012264. PubMed ID: 31865891
[TBL] [Abstract][Full Text] [Related]
5. Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing.
Coll M; Allegue C; Partemi S; Mates J; Del Olmo B; Campuzano O; Pascali V; Iglesias A; Striano P; Oliva A; Brugada R
Int J Legal Med; 2016 Mar; 130(2):331-9. PubMed ID: 26423924
[TBL] [Abstract][Full Text] [Related]
6. Genetic variants in incident SUDEP cases from a community-based prospective cohort with epilepsy.
Ge Y; Ding D; Zhu G; Kwan P; Wang W; Hong Z; Sander JW
J Neurol Neurosurg Psychiatry; 2020 Feb; 91(2):126-131. PubMed ID: 31776209
[TBL] [Abstract][Full Text] [Related]
7. Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the
Smith JL; Tester DJ; Hall AR; Burgess DE; Hsu CC; Elayi SC; Anderson CL; January CT; Luo JZ; Hartzel DN; Mirshahi UL; Murray MF; Mirshahi T; Ackerman MJ; Delisle BP
Circ Arrhythm Electrophysiol; 2018 May; 11(5):e005859. PubMed ID: 29752375
[TBL] [Abstract][Full Text] [Related]
8. Rare sudden unexpected death in epilepsy SCN5A variants cause changes in channel function implicating cardiac arrhythmia as a cause of death.
Soh MS; Bagnall RD; Semsarian C; Scheffer IE; Berkovic SF; Reid CA
Epilepsia; 2022 Jun; 63(6):e57-e62. PubMed ID: 35397174
[TBL] [Abstract][Full Text] [Related]
9. Cardiac arrhythmia and epilepsy genetic variants in sudden unexpected death in epilepsy.
Aschner A; Keller A; Williams A; Whitney R; Cunningham K; Hamilton RM; Pollanen M; Donner E
Front Neurol; 2024; 15():1386730. PubMed ID: 38756210
[TBL] [Abstract][Full Text] [Related]
10. Temporal trends and autopsy findings of SUDEP based on medico-legal investigations in the United States.
Cihan E; Devinsky O; Hesdorffer DC; Brandsoy M; Li L; Fowler DR; Graham JK; Karlovich MW; Yang JE; Keller AE; Donner EJ; Friedman D
Neurology; 2020 Aug; 95(7):e867-e877. PubMed ID: 32636323
[TBL] [Abstract][Full Text] [Related]
11. The influence of risk factors, biomarkers and care settings on SUDEP counseling.
Valdrighi A; Laze J; Farooque P; Friedman D; Devinsky O; Singhal N; Hegde M
Epilepsy Behav; 2024 Jul; 156():109845. PubMed ID: 38788665
[TBL] [Abstract][Full Text] [Related]
12. Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy.
Leu C; Balestrini S; Maher B; Hernández-Hernández L; Gormley P; Hämäläinen E; Heggeli K; Schoeler N; Novy J; Willis J; Plagnol V; Ellis R; Reavey E; O'Regan M; Pickrell WO; Thomas RH; Chung SK; Delanty N; McMahon JM; Malone S; Sadleir LG; Berkovic SF; Nashef L; Zuberi SM; Rees MI; Cavalleri GL; Sander JW; Hughes E; Helen Cross J; Scheffer IE; Palotie A; Sisodiya SM
EBioMedicine; 2015 Sep; 2(9):1063-70. PubMed ID: 26501104
[TBL] [Abstract][Full Text] [Related]
13. Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population.
Wang F; Liu Y; Liao H; Xue Y; Zhan X; Fang X; Liang Y; Wei W; Rao F; Zhang Q; Deng H; Lin Y; Liu F; Lin W; Zhang B; Wu S
Cardiology; 2020; 145(1):38-45. PubMed ID: 31751991
[TBL] [Abstract][Full Text] [Related]
14. Sudden unexpected death in epilepsy (SUDEP) in New Zealand; a retrospective review.
Brennan M; Scott S; Bergin P
N Z Med J; 2020 Jan; 133(1508):65-71. PubMed ID: 31945043
[TBL] [Abstract][Full Text] [Related]
15. ANK2 functionally interacts with KCNH2 aggravating long QT syndrome in a double mutation carrier.
Gessner G; Runge S; Koenen M; Heinemann SH; Koenen M; Haas J; Meder B; Thomas D; Katus HA; Schweizer PA
Biochem Biophys Res Commun; 2019 May; 512(4):845-851. PubMed ID: 30929919
[TBL] [Abstract][Full Text] [Related]
16. Autopsy-reported cause of death in a population-based cohort of sudden unexpected death in epilepsy.
Keller AE; Ho J; Whitney R; Li SA; Williams AS; Pollanen MS; Donner EJ
Epilepsia; 2021 Feb; 62(2):472-480. PubMed ID: 33400291
[TBL] [Abstract][Full Text] [Related]
17. Sudden unexpected death in epilepsy. A nationwide population-based study.
Einarsdottir AB; Sveinsson O; Olafsson E
Epilepsia; 2019 Nov; 60(11):2174-2181. PubMed ID: 31571204
[TBL] [Abstract][Full Text] [Related]
18. Sudden unexpected death in epilepsy: Incidence at a Spanish epilepsy unit.
Chamorro-Muñoz MI; López-Hidalgo E; García-Martín G; Rodríguez-Belli AO; Gutiérrez-Bedmar M
Neurologia (Engl Ed); 2020 Sep; 35(7):464-469. PubMed ID: 29248207
[TBL] [Abstract][Full Text] [Related]
19. The role of P-glycoprotein (P-gp) and inwardly rectifying potassium (Kir) channels in sudden unexpected death in epilepsy (SUDEP).
Auzmendi J; Akyuz E; Lazarowski A
Epilepsy Behav; 2021 Aug; 121(Pt B):106590. PubMed ID: 31706919
[TBL] [Abstract][Full Text] [Related]
20. Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign.
Mattivi CL; Ye D; Tester DJ; Clemens DJ; Zhou W; Giudicessi JR; Ackerman MJ
Heart Rhythm; 2020 Feb; 17(2):315-323. PubMed ID: 31493592
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
