These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
484 related articles for article (PubMed ID: 23933820)
1. GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction. Lesca G; Rudolf G; Bruneau N; Lozovaya N; Labalme A; Boutry-Kryza N; Salmi M; Tsintsadze T; Addis L; Motte J; Wright S; Tsintsadze V; Michel A; Doummar D; Lascelles K; Strug L; Waters P; de Bellescize J; Vrielynck P; de Saint Martin A; Ville D; Ryvlin P; Arzimanoglou A; Hirsch E; Vincent A; Pal D; Burnashev N; Sanlaville D; Szepetowski P Nat Genet; 2013 Sep; 45(9):1061-6. PubMed ID: 23933820 [TBL] [Abstract][Full Text] [Related]
2. Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutations. Lesca G; Møller RS; Rudolf G; Hirsch E; Hjalgrim H; Szepetowski P Epileptic Disord; 2019 Jun; 21(S1):41-47. PubMed ID: 31149903 [TBL] [Abstract][Full Text] [Related]
3. A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia. Gao K; Tankovic A; Zhang Y; Kusumoto H; Zhang J; Chen W; XiangWei W; Shaulsky GH; Hu C; Traynelis SF; Yuan H; Jiang Y PLoS One; 2017; 12(2):e0170818. PubMed ID: 28182669 [TBL] [Abstract][Full Text] [Related]
4. Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism. Lesca G; Rudolf G; Labalme A; Hirsch E; Arzimanoglou A; Genton P; Motte J; de Saint Martin A; Valenti MP; Boulay C; De Bellescize J; Kéo-Kosal P; Boutry-Kryza N; Edery P; Sanlaville D; Szepetowski P Epilepsia; 2012 Sep; 53(9):1526-38. PubMed ID: 22738016 [TBL] [Abstract][Full Text] [Related]
5. GRIN2A mutations in epilepsy-aphasia spectrum disorders. Yang X; Qian P; Xu X; Liu X; Wu X; Zhang Y; Yang Z Brain Dev; 2018 Mar; 40(3):205-210. PubMed ID: 29056244 [TBL] [Abstract][Full Text] [Related]
7. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Lemke JR; Lal D; Reinthaler EM; Steiner I; Nothnagel M; Alber M; Geider K; Laube B; Schwake M; Finsterwalder K; Franke A; Schilhabel M; Jähn JA; Muhle H; Boor R; Van Paesschen W; Caraballo R; Fejerman N; Weckhuysen S; De Jonghe P; Larsen J; Møller RS; Hjalgrim H; Addis L; Tang S; Hughes E; Pal DK; Veri K; Vaher U; Talvik T; Dimova P; Guerrero López R; Serratosa JM; Linnankivi T; Lehesjoki AE; Ruf S; Wolff M; Buerki S; Wohlrab G; Kroell J; Datta AN; Fiedler B; Kurlemann G; Kluger G; Hahn A; Haberlandt DE; Kutzer C; Sperner J; Becker F; Weber YG; Feucht M; Steinböck H; Neophythou B; Ronen GM; Gruber-Sedlmayr U; Geldner J; Harvey RJ; Hoffmann P; Herms S; Altmüller J; Toliat MR; Thiele H; Nürnberg P; Wilhelm C; Stephani U; Helbig I; Lerche H; Zimprich F; Neubauer BA; Biskup S; von Spiczak S Nat Genet; 2013 Sep; 45(9):1067-72. PubMed ID: 23933819 [TBL] [Abstract][Full Text] [Related]
8. From rolandic epilepsy to continuous spike-and-waves during sleep and Landau-Kleffner syndromes: insights into possible genetic factors. Rudolf G; Valenti MP; Hirsch E; Szepetowski P Epilepsia; 2009 Aug; 50 Suppl 7():25-8. PubMed ID: 19682046 [TBL] [Abstract][Full Text] [Related]
9. Epilepsy: GRIN2A mutations identified as key genetic drivers of epilepsy-aphasia spectrum disorders. Kingwell K Nat Rev Neurol; 2013 Oct; 9(10):541. PubMed ID: 23999465 [No Abstract] [Full Text] [Related]
10. De novo GRIN2A variants associated with epilepsy and autism and literature review. Mangano GD; Riva A; Fontana A; Salpietro V; Mangano GR; Nobile G; Orsini A; Iacomino M; Battini R; Astrea G; Striano P; Nardello R Epilepsy Behav; 2022 Apr; 129():108604. PubMed ID: 35217385 [TBL] [Abstract][Full Text] [Related]
11. [Study of GRIN2A mutation in epilepsy-aphasia spectrum disorders]. Qian P; Yang X; Xu X; Liu X; Zhang Y; Yang Z Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Jun; 35(3):314-318. PubMed ID: 29896722 [TBL] [Abstract][Full Text] [Related]
12. GRIN2A-related epilepsy and speech disorders: A comprehensive overview with a focus on the role of precision therapeutics. Samanta D Epilepsy Res; 2023 Jan; 189():107065. PubMed ID: 36516565 [TBL] [Abstract][Full Text] [Related]
13. Mild neurological phenotype in a family carrying a novel N-terminal null GRIN2A variant. De Bernardi ML; Di Stazio A; Romano A; Minardi R; Bisulli F; Licchetta L; Aiello S; Carelli V; Brunetti-Pierri N; Cappuccio G; Terrone G Eur J Med Genet; 2022 May; 65(5):104500. PubMed ID: 35367634 [TBL] [Abstract][Full Text] [Related]
15. Transient microstructural brain anomalies and epileptiform discharges in mice defective for epilepsy and language-related NMDA receptor subunit gene Grin2a. Salmi M; Bolbos R; Bauer S; Minlebaev M; Burnashev N; Szepetowski P Epilepsia; 2018 Oct; 59(10):1919-1930. PubMed ID: 30146685 [TBL] [Abstract][Full Text] [Related]
16. Clinical Forms and Li X; Xie LL; Han W; Hong SQ; Ma JN; Wang J; Jiang L Front Pediatr; 2020; 8():574803. PubMed ID: 33240831 [No Abstract] [Full Text] [Related]
17. Early-onset acquired epileptic aphasia (Landau-Kleffner syndrome, LKS) and regressive autistic disorders with epileptic EEG abnormalities: the continuing debate. Deonna T; Roulet-Perez E Brain Dev; 2010 Oct; 32(9):746-52. PubMed ID: 20637551 [TBL] [Abstract][Full Text] [Related]
18. Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region. Reutlinger C; Helbig I; Gawelczyk B; Subero JI; Tönnies H; Muhle H; Finsterwalder K; Vermeer S; Pfundt R; Sperner J; Stefanova I; Gillessen-Kaesbach G; von Spiczak S; van Baalen A; Boor R; Siebert R; Stephani U; Caliebe A Epilepsia; 2010 Sep; 51(9):1870-3. PubMed ID: 20384727 [TBL] [Abstract][Full Text] [Related]
19. GRIN2A, a green semaphore on the lumping route to idiopathic focal epilepsy in childhood. Vercueil L Rev Neurol (Paris); 2013 Dec; 169(12):921-2. PubMed ID: 24239346 [No Abstract] [Full Text] [Related]
20. Exome sequencing in 57 patients with self-limited focal epilepsies of childhood with typical or atypical presentations suggests novel candidate genes. Rudolf G; de Bellescize J; de Saint Martin A; Arzimanoglou A; Valenti Hirsch MP; Labalme A; Boulay C; Simonet T; Boland A; Deleuze JF; Nitschké P; Ollivier E; Sanlaville D; Hirsch E; Chelly J; Lesca G Eur J Paediatr Neurol; 2020 Jul; 27():104-110. PubMed ID: 32600977 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]