448 related articles for article (PubMed ID: 28524223)
1. [Infantile epileptic encephalopathies: what matters is genetics].
Garcia-Penas JJ; Jimenez-Legido M
Rev Neurol; 2017 May; 64(s03):S65-S69. PubMed ID: 28524223
[TBL] [Abstract][Full Text] [Related]
2. [Trends and expectations the research on the molecular background of epileptic encephalopathies - state of the art in 2017].
Hoffman-Zacharska D; Górka-Skoczylas P
Dev Period Med; 2017; 21(4):317-327. PubMed ID: 29291359
[TBL] [Abstract][Full Text] [Related]
3. [How must we manage epileptic encephalopathies in infants? Conclusions].
Soto-Insuga V
Rev Neurol; 2017 May; 64(s03):S77-S80. PubMed ID: 28524225
[TBL] [Abstract][Full Text] [Related]
4. Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy.
Gürsoy S; Erçal D
J Child Neurol; 2016 Mar; 31(4):523-32. PubMed ID: 26271793
[TBL] [Abstract][Full Text] [Related]
5. Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies.
Zhou P; He N; Zhang JW; Lin ZJ; Wang J; Yan LM; Meng H; Tang B; Li BM; Liu XR; Shi YW; Zhai QX; Yi YH; Liao WP
Genes Brain Behav; 2018 Nov; 17(8):e12456. PubMed ID: 29314583
[TBL] [Abstract][Full Text] [Related]
6. [Epileptic encephalopathies].
Ramos-Lizana J
Rev Neurol; 2017 May; 64(s03):S45-S48. PubMed ID: 28524219
[TBL] [Abstract][Full Text] [Related]
7. [Epileptic encephalopathies of onset in neonates and infants].
Guerrero Ruiz GDP
Medicina (B Aires); 2022 Aug; 82 Suppl 3():13-18. PubMed ID: 36054851
[TBL] [Abstract][Full Text] [Related]
8. [Neuroimaging in epileptic encephalopathies in infants].
Lopez-Pino MA; Garcia-Esparza E
Rev Neurol; 2017 May; 64(s03):S61-S64. PubMed ID: 28524222
[TBL] [Abstract][Full Text] [Related]
9. The Expanding Clinical Spectrum of Genetic Pediatric Epileptic Encephalopathies.
Shbarou R; Mikati MA
Semin Pediatr Neurol; 2016 May; 23(2):134-42. PubMed ID: 27544470
[TBL] [Abstract][Full Text] [Related]
10. Genotype-phenotype correlates of infantile-onset developmental & epileptic encephalopathy syndromes in South India: A single centre experience.
Mitta N; Menon RN; McTague A; Radhakrishnan A; Sundaram S; Cherian A; Madhavilatha GK; Mannan AU; Nampoothiri S; Thomas SV
Epilepsy Res; 2020 Oct; 166():106398. PubMed ID: 32593896
[TBL] [Abstract][Full Text] [Related]
11. Current understanding and neurobiology of epileptic encephalopathies.
Auvin S; Cilio MR; Vezzani A
Neurobiol Dis; 2016 Aug; 92(Pt A):72-89. PubMed ID: 26992889
[TBL] [Abstract][Full Text] [Related]
12. Summary of recommendations for the management of infantile seizures: Task Force Report for the ILAE Commission of Pediatrics.
Wilmshurst JM; Gaillard WD; Vinayan KP; Tsuchida TN; Plouin P; Van Bogaert P; Carrizosa J; Elia M; Craiu D; Jovic NJ; Nordli D; Hirtz D; Wong V; Glauser T; Mizrahi EM; Cross JH
Epilepsia; 2015 Aug; 56(8):1185-97. PubMed ID: 26122601
[TBL] [Abstract][Full Text] [Related]
13. Early-onset epileptic encephalopathies and the diagnostic approach to underlying causes.
Hwang SK; Kwon S
Korean J Pediatr; 2015 Nov; 58(11):407-14. PubMed ID: 26692875
[TBL] [Abstract][Full Text] [Related]
14. Malignant epileptic encephalopathies in children.
Dulac OJ; Chiron C
Baillieres Clin Neurol; 1996 Dec; 5(4):765-81. PubMed ID: 9068880
[TBL] [Abstract][Full Text] [Related]
15. Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy.
Bayat A; Bayat M; Rubboli G; Møller RS
Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356067
[TBL] [Abstract][Full Text] [Related]
16. Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.
Olson HE; Kelly M; LaCoursiere CM; Pinsky R; Tambunan D; Shain C; Ramgopal S; Takeoka M; Libenson MH; Julich K; Loddenkemper T; Marsh ED; Segal D; Koh S; Salman MS; Paciorkowski AR; Yang E; Bergin AM; Sheidley BR; Poduri A
Ann Neurol; 2017 Mar; 81(3):419-429. PubMed ID: 28133863
[TBL] [Abstract][Full Text] [Related]
17. Novel Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotypes.
Mastrangelo M
Pediatr Neurol; 2015 Aug; 53(2):119-29. PubMed ID: 26073591
[TBL] [Abstract][Full Text] [Related]
18. [Genetically determined epileptic encephalopathies].
Appendino JP; Appendino JI
Medicina (B Aires); 2019; 79 Suppl 3():42-47. PubMed ID: 31603843
[TBL] [Abstract][Full Text] [Related]
19. Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results.
Gerald B; Ramsey K; Belnap N; Szelinger S; Siniard AL; Balak C; Russell M; Richholt R; De Both M; Claasen AM; Schrauwen I; Huentelman MJ; Craig DW; Rangasamy S; Narayanan V
Semin Pediatr Neurol; 2018 Jul; 26():28-32. PubMed ID: 29961512
[TBL] [Abstract][Full Text] [Related]
20. The severe epilepsy syndromes of infancy: A population-based study.
Howell KB; Freeman JL; Mackay MT; Fahey MC; Archer J; Berkovic SF; Chan E; Dabscheck G; Eggers S; Hayman M; Holberton J; Hunt RW; Jacobs SE; Kornberg AJ; Leventer RJ; Mandelstam S; McMahon JM; Mefford HC; Panetta J; Riseley J; Rodriguez-Casero V; Ryan MM; Schneider AL; Smith LJ; Stark Z; Wong F; Yiu EM; Scheffer IE; Harvey AS
Epilepsia; 2021 Feb; 62(2):358-370. PubMed ID: 33475165
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
