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Journal Abstract Search

242 related items for PubMed ID: 33240831

  • 1.
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  • 3. [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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  • 4. Idiopathic encephalopathy related to status epilepticus during slow sleep (ESES) as a "pure" model of epileptic encephalopathy. An electroclinical, genetic, and follow-up study.
    Pavlidis E, Møller RS, Nikanorova M, Kölmel MS, Stendevad P, Beniczky S, Tassinari CA, Rubboli G, Gardella E.
    Epilepsy Behav; 2019 Aug 10; 97():244-252. PubMed ID: 31254844
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  • 6. 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 01; 21(S1):41-47. PubMed ID: 31149903
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  • 7. 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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  • 8. 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 01; 45(9):1067-72. PubMed ID: 23933819
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  • 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 01; 65(5):104500. PubMed ID: 35367634
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  • 11. 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 01; 45(9):1061-6. PubMed ID: 23933820
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  • 13. Immunotherapy for GRIN2A and GRIN2D-related epileptic encephalopathy.
    Hausman-Kedem M, Menascu S, Greenstein Y, Fattal-Valevski A.
    Epilepsy Res; 2020 Jul 01; 163():106325. PubMed ID: 32289570
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  • 14. [Epileptic syndromes which show continuous spike and wake complexes during slow wave sleep].
    Nieto-Barrera M, Aguilar-Quero F, Montes E, Candau R, Prieto P.
    Rev Neurol; 1997 Jul 01; 25(143):1045-51. PubMed ID: 9280631
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  • 16. [Speech and language neurodevelopmental disorders in epilepsy: pathophysiologic mechanisms and therapeutic approaches].
    Zavadenko NN, Kholin AA, Zavadenko AN, Michurina ES.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2018 Jul 01; 118(8):118-125. PubMed ID: 30251989
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  • 17. GRIN2A-related epilepsy and speech disorders: A comprehensive overview with a focus on the role of precision therapeutics.
    Samanta D.
    Epilepsy Res; 2023 Jan 01; 189():107065. PubMed ID: 36516565
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  • 19. Landau-Kleffner syndrome: a study of 29 patients.
    Caraballo RH, Cejas N, Chamorro N, Kaltenmeier MC, Fortini S, Soprano AM.
    Seizure; 2014 Feb 01; 23(2):98-104. PubMed ID: 24315829
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  • 20. [Efficacy of methylprednisolone therapy for electrical status epilepticus during sleep in children].
    Chen J, Yang Z, Liu X, Ji T, Fu N, Wu Y, Xiong H, Wang S, Chang X, Zhang Y, Bao X, Jiang Y, Qin J.
    Zhonghua Er Ke Za Zhi; 2014 Sep 01; 52(9):678-82. PubMed ID: 25476430
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