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161 related items for PubMed ID: 36516565

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. 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
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  • 4.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Strehlow V, Myers KA, Morgan AT, Scheffer IE, Lemke JR.
    ; 1993 May. PubMed ID: 27683935
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  • 9. 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
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  • 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 10; 35(3):314-318. PubMed ID: 29896722
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  • 13. 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 10; 59(10):1919-1930. PubMed ID: 30146685
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