177 related articles for article (PubMed ID: 30146685)
1. 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]
2. Impaired vocal communication, sleep-related discharges, and transient alteration of slow-wave sleep in developing mice lacking the GluN2A subunit of N-methyl-d-aspartate receptors.
Salmi M; Del Gallo F; Minlebaev M; Zakharov A; Pauly V; Perron P; Pons-Bennaceur A; Corby-Pellegrino S; Aniksztejn L; Lenck-Santini PP; Epsztein J; Khazipov R; Burnashev N; Bertini G; Szepetowski P
Epilepsia; 2019 Jul; 60(7):1424-1437. PubMed ID: 31158310
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
Carvill GL; Regan BM; Yendle SC; O'Roak BJ; Lozovaya N; Bruneau N; Burnashev N; Khan A; Cook J; Geraghty E; Sadleir LG; Turner SJ; Tsai MH; Webster R; Ouvrier R; Damiano JA; Berkovic SF; Shendure J; Hildebrand MS; Szepetowski P; Scheffer IE; Mefford HC
Nat Genet; 2013 Sep; 45(9):1073-6. PubMed ID: 23933818
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [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]
7. 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]
8. 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]
9. 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]
10. Response to immunotherapy in a patient with Landau-Kleffner syndrome and GRIN2A mutation.
Fainberg N; Harper A; Tchapyjnikov D; Mikati MA
Epileptic Disord; 2016 Mar; 18(1):97-100. PubMed ID: 26806548
[TBL] [Abstract][Full Text] [Related]
11. 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]
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. 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]
14. A novel missense mutation in GRIN2A causes a nonepileptic neurodevelopmental disorder.
Fernández-Marmiesse A; Kusumoto H; Rekarte S; Roca I; Zhang J; Myers SJ; Traynelis SF; Couce ML; Gutierrez-Solana L; Yuan H
Mov Disord; 2018 Jul; 33(6):992-999. PubMed ID: 29644724
[TBL] [Abstract][Full Text] [Related]
15. GRIN2A-related disorders: genotype and functional consequence predict phenotype.
Strehlow V; Heyne HO; Vlaskamp DRM; Marwick KFM; Rudolf G; de Bellescize J; Biskup S; Brilstra EH; Brouwer OF; Callenbach PMC; Hentschel J; Hirsch E; Kind PC; Mignot C; Platzer K; Rump P; Skehel PA; Wyllie DJA; Hardingham GE; van Ravenswaaij-Arts CMA; Lesca G; Lemke JR;
Brain; 2019 Jan; 142(1):80-92. PubMed ID: 30544257
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. New genes for focal epilepsies with speech and language disorders.
Turner SJ; Morgan AT; Perez ER; Scheffer IE
Curr Neurol Neurosci Rep; 2015 Jun; 15(6):35. PubMed ID: 25921602
[TBL] [Abstract][Full Text] [Related]
18. Epileptic encephalopathy with continuous spike-waves during slow-wave sleep including Landau-Kleffner syndrome.
Van Bogaert P
Handb Clin Neurol; 2013; 111():635-40. PubMed ID: 23622211
[TBL] [Abstract][Full Text] [Related]
19. Immunotherapy for GRIN2A and GRIN2D-related epileptic encephalopathy.
Hausman-Kedem M; Menascu S; Greenstein Y; Fattal-Valevski A
Epilepsy Res; 2020 Jul; 163():106325. PubMed ID: 32289570
[TBL] [Abstract][Full Text] [Related]
20. Cnksr2 Loss in Mice Leads to Increased Neural Activity and Behavioral Phenotypes of Epilepsy-Aphasia Syndrome.
Erata E; Gao Y; Purkey AM; Soderblom EJ; McNamara JO; Soderling SH
J Neurosci; 2021 Nov; 41(46):9633-9649. PubMed ID: 34580165
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
