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Journal Abstract Search

161 related items for PubMed ID: 36516565

  • 21. Successful Treatment of a Child With Epileptic Encephalopathy With Spike-Wave Activation in Sleep and GRIN2A Variant Using Sulthiame.
    Pereira-Nunes J, Sousa JM, Fonseca J, Melo C, Alves D, Sampaio M, Sousa R.
    Cureus; 2023 Feb; 15(2):e34686. PubMed ID: 36909045
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  • 22. Differential functional consequences of GRIN2A mutations associated with schizophrenia and neurodevelopmental disorders.
    Shepard N, Baez-Nieto D, Iqbal S, Kurganov E, Budnik N, Campbell AJ, Pan JQ, Sheng M, Farsi Z.
    Sci Rep; 2024 Feb 02; 14(1):2798. PubMed ID: 38307912
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  • 23. Functional Properties of Human NMDA Receptors Associated with Epilepsy-Related Mutations of GluN2A Subunit.
    Sibarov DA, Bruneau N, Antonov SM, Szepetowski P, Burnashev N, Giniatullin R.
    Front Cell Neurosci; 2017 Feb 02; 11():155. PubMed ID: 28611597
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  • 28. Modelling and treating GRIN2A developmental and epileptic encephalopathy in mice.
    Amador A, Bostick CD, Olson H, Peters J, Camp CR, Krizay D, Chen W, Han W, Tang W, Kanber A, Kim S, Teoh J, Sah M, Petri S, Paek H, Kim A, Lutz CM, Yang M, Myers SJ, Bhattacharya S, Yuan H, Goldstein DB, Poduri A, Boland MJ, Traynelis SF, Frankel WN.
    Brain; 2020 Jul 01; 143(7):2039-2057. PubMed ID: 32577763
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  • 29. Clinical genetic study of the epilepsy-aphasia spectrum.
    Tsai MH, Vears DF, Turner SJ, Smith RL, Berkovic SF, Sadleir LG, Scheffer IE.
    Epilepsia; 2013 Feb 01; 54(2):280-7. PubMed ID: 23294109
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  • 30. 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 01; 18(1):97-100. PubMed ID: 26806548
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  • 31. An Epilepsy-Associated GRIN2A Rare Variant Disrupts CaMKIIα Phosphorylation of GluN2A and NMDA Receptor Trafficking.
    Mota Vieira M, Nguyen TA, Wu K, Badger JD, Collins BM, Anggono V, Lu W, Roche KW.
    Cell Rep; 2020 Sep 01; 32(9):108104. PubMed ID: 32877683
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  • 33. Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.
    von Stülpnagel C, Ensslen M, Møller RS, Pal DK, Masnada S, Veggiotti P, Piazza E, Dreesmann M, Hartlieb T, Herberhold T, Hughes E, Koch M, Kutzer C, Hoertnagel K, Nitanda J, Pohl M, Rostásy K, Haack TB, Stöhr K, Kluger G, Borggraefe I.
    Eur J Paediatr Neurol; 2017 May 01; 21(3):530-541. PubMed ID: 28109652
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  • 34. Efavirenz restored NMDA receptor dysfunction and inhibited epileptic seizures in GluN2A/Grin2a mutant mice.
    Zhao T, Zhong R, Zhang X, Li G, Zhou C, Fang S, Ding Y, Lin W.
    Front Neurosci; 2023 May 01; 17():1086462. PubMed ID: 36937661
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  • 35. Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency - molecular profiling and functional rescue.
    Addis L, Virdee JK, Vidler LR, Collier DA, Pal DK, Ursu D.
    Sci Rep; 2017 Feb 27; 7(1):66. PubMed ID: 28242877
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  • 36. GRIN2A Variant in A 3-Year-Old-An Expanding Spectrum?
    Gheța I, Teleanu RI, Roza E, Carapancea E, Vladacenco O, Teleanu DM.
    Neurol Int; 2021 Apr 29; 13(2):184-189. PubMed ID: 33946630
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  • 37. Acquired epileptic opercular syndrome related to a heterozygous deleterious substitution in GRIN2A.
    Sculier C, Tilmant AS, De Tiège X, Giurgea S, Paquier P, Rudolf G, Lesca G, Van Bogaert P.
    Epileptic Disord; 2017 Sep 01; 19(3):345-350. PubMed ID: 28832001
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  • 38. Two patients with a GRIN2A mutation and childhood-onset epilepsy.
    DeVries SP, Patel AD.
    Pediatr Neurol; 2013 Dec 01; 49(6):482-5. PubMed ID: 24125812
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  • 39. Mouse mutants in schizophrenia risk genes GRIN2A and AKAP11 show EEG abnormalities in common with schizophrenia patients.
    Herzog LE, Wang L, Yu E, Choi S, Farsi Z, Song BJ, Pan JQ, Sheng M.
    Transl Psychiatry; 2023 Mar 13; 13(1):92. PubMed ID: 36914641
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  • 40. GRIN2A -Related Severe Epileptic Encephalopathy Treated with Memantine: An Example of Precision Medicine.
    Mir A, Qahtani M, Bashir S.
    J Pediatr Genet; 2020 Dec 13; 9(4):252-257. PubMed ID: 32765929
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