222 related articles for article (PubMed ID: 32979071)
1. Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay.
Kobow K; Jabari S; Pieper T; Kudernatsch M; Polster T; Woermann FG; Kalbhenn T; Hamer H; Rössler K; Mühlebner A; Spliet WGM; Feucht M; Hou Y; Stichel D; Korshunov A; Sahm F; Coras R; Blümcke I; von Deimling A
Acta Neuropathol; 2020 Dec; 140(6):881-891. PubMed ID: 32979071
[TBL] [Abstract][Full Text] [Related]
2. Surgical management of medically refractory epilepsy in patients with polymicrogyria.
Wang DD; Knox R; Rolston JD; Englot DJ; Barkovich AJ; Tihan T; Auguste KI; Knowlton RC; Cornes SB; Chang EF
Epilepsia; 2016 Jan; 57(1):151-61. PubMed ID: 26647903
[TBL] [Abstract][Full Text] [Related]
3. Comprehensive molecular screening strategy of OCLN in band-like calcification with simplified gyration and polymicrogyria.
Jenkinson EM; Livingston JH; O'Driscoll MC; Desguerre I; Nabbout R; Boddaert N; Soares G; Gonçalves da Rocha M; D'Arrigo S; Rice GI; Crow YJ
Clin Genet; 2018 Feb; 93(2):228-234. PubMed ID: 28386946
[TBL] [Abstract][Full Text] [Related]
4. Stereoelectroencephalography and surgical outcome in polymicrogyria-related epilepsy: A multicentric study.
Maillard LG; Tassi L; Bartolomei F; Catenoix H; Dubeau F; Szurhaj W; Kahane P; Nica A; Marusic P; Mindruta I; Chassoux F; Ramantani G
Ann Neurol; 2017 Nov; 82(5):781-794. PubMed ID: 29059488
[TBL] [Abstract][Full Text] [Related]
5. Polymicrogyria-associated epilepsy: a multicenter phenotypic study from the Epilepsy Phenome/Genome Project.
Shain C; Ramgopal S; Fallil Z; Parulkar I; Alongi R; Knowlton R; Poduri A;
Epilepsia; 2013 Aug; 54(8):1368-75. PubMed ID: 23750890
[TBL] [Abstract][Full Text] [Related]
6. Epilepsy surgery for polymicrogyria: a challenge to be undertaken.
Maillard L; Ramantani G
Epileptic Disord; 2018 Oct; 20(5):319-338. PubMed ID: 30378553
[TBL] [Abstract][Full Text] [Related]
7. Hemispheric polymicrogyria and neonatal seizures: a potentially life-threatening combination.
Brna PM; Harvey AS; Leventer RJ
Epileptic Disord; 2017 Mar; 19(1):87-93. PubMed ID: 28300030
[TBL] [Abstract][Full Text] [Related]
8. Polymicrogyria is Associated With Pathogenic Variants in PTEN.
Shao DD; Achkar CM; Lai A; Srivastava S; Doan RN; Rodan LH; Chen AY; ; Poduri A; Yang E; Walsh CA
Ann Neurol; 2020 Dec; 88(6):1153-1164. PubMed ID: 32959437
[TBL] [Abstract][Full Text] [Related]
9. An autopsy case of refractory epilepsy due to unilateral polymicrogyria in a 65-year-old man: Histogenesis of four-layered polymicrogyric cortex.
Miki Y; Tanji K; Mori F; Sakamoto N; Wakabayashi K
Neuropathology; 2015 Dec; 35(6):569-74. PubMed ID: 26094545
[TBL] [Abstract][Full Text] [Related]
10. The role of surgery in refractory epilepsy secondary to polymicrogyria in the pediatric population.
Jalloh I; Cho N; Nga VDW; Whitney R; Jain P; Al-Mehmadi S; Yau I; Okura H; Widjaja E; Otsubo H; Ochi A; Donner E; McCoy B; Drake J; Go C; Rutka JT
Epilepsia; 2018 Oct; 59(10):1982-1996. PubMed ID: 30203507
[TBL] [Abstract][Full Text] [Related]
11. Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care.
Pirozzi F; Berkseth M; Shear R; Gonzalez L; Timms AE; Sulc J; Pao E; Oyama N; Forzano F; Conti V; Guerrini R; Doherty ES; Saitta SC; Lockwood CM; Pritchard CC; Dobyns WB; Novotny E; Wright JNN; Saneto RP; Friedman S; Hauptman J; Ojemann J; Kapur RP; Mirzaa GM
Brain; 2022 Apr; 145(3):925-938. PubMed ID: 35355055
[TBL] [Abstract][Full Text] [Related]
12. The genomic landscape across 474 surgically accessible epileptogenic human brain lesions.
López-Rivera JA; Leu C; Macnee M; Khoury J; Hoffmann L; Coras R; Kobow K; Bhattarai N; Pérez-Palma E; Hamer H; Brandner S; Rössler K; Bien CG; Kalbhenn T; Pieper T; Hartlieb T; Butler E; Genovese G; Becker K; Altmüller J; Niestroj LM; Ferguson L; Busch RM; Nürnberg P; Najm I; Blümcke I; Lal D
Brain; 2023 Apr; 146(4):1342-1356. PubMed ID: 36226386
[TBL] [Abstract][Full Text] [Related]
13. Intracranial evaluation of the epileptogenic zone in regional infrasylvian polymicrogyria.
Ramantani G; Koessler L; Colnat-Coulbois S; Vignal JP; Isnard J; Catenoix H; Jonas J; Zentner J; Schulze-Bonhage A; Maillard LG
Epilepsia; 2013 Feb; 54(2):296-304. PubMed ID: 22988886
[TBL] [Abstract][Full Text] [Related]
14. Identification of a somatic mutation in the RHEB gene through high depth and ultra-high depth next generation sequencing in a patient with Hemimegalencephaly and drug resistant Epilepsy.
Salinas V; Vega P; Piccirilli MV; Chicco C; Ciraolo C; Christiansen S; Consalvo D; Perez-Maturo J; Medina N; González-Morón D; Novaro V; Perrone C; García MDC; Agosta G; Silva W; Kauffman M
Eur J Med Genet; 2019 Nov; 62(11):103571. PubMed ID: 30414531
[TBL] [Abstract][Full Text] [Related]
15. A novel splice variant expands the LAMC3-associated cortical phenotype to frontal only polymicrogyria and adult-onset epilepsy.
Kasper BS; Kraus C; Schwarz M; Rösch J; Thiel CT; Reis A; Zweier C
Am J Med Genet A; 2020 Nov; 182(11):2761-2764. PubMed ID: 32902107
[TBL] [Abstract][Full Text] [Related]
16. Altered white matter connectivity and network organization in polymicrogyria revealed by individual gyral topology-based analysis.
Im K; Paldino MJ; Poduri A; Sporns O; Grant PE
Neuroimage; 2014 Feb; 86():182-93. PubMed ID: 23954485
[TBL] [Abstract][Full Text] [Related]
17. Long-term outcome characteristics in mesial temporal lobe epilepsy with and without associated cortical dysplasia.
Schmeiser B; Hammen T; Steinhoff BJ; Zentner J; Schulze-Bonhage A
Epilepsy Res; 2016 Oct; 126():147-56. PubMed ID: 27500381
[TBL] [Abstract][Full Text] [Related]
18. Polymicrogyria: a common and heterogeneous malformation of cortical development.
Stutterd CA; Leventer RJ
Am J Med Genet C Semin Med Genet; 2014 Jun; 166C(2):227-39. PubMed ID: 24888723
[TBL] [Abstract][Full Text] [Related]
19. Parasagittal hemispherotomy in hemispheric polymicrogyria with electrical status epilepticus during slow sleep: Indications, results and follow-up.
Fohlen M; Dorfmüller G; Ferrand-Sorbets S; Dorison N; Chipaux M; Taussig D
Seizure; 2019 Oct; 71():190-200. PubMed ID: 31386962
[TBL] [Abstract][Full Text] [Related]
20. The specific DNA methylation landscape in focal cortical dysplasia ILAE type 3D.
Wang DD; Katoch M; Jabari S; Blumcke I; Blumenthal DB; Lu DH; Coras R; Wang YJ; Shi J; Zhou WJ; Kobow K; Piao YS
Acta Neuropathol Commun; 2023 Aug; 11(1):129. PubMed ID: 37559109
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]