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Journal Abstract Search

138 related items for PubMed ID: 38088023

  • 1. Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing.
    Coppola A, Krithika S, Iacomino M, Bobbili D, Balestrini S, Bagnasco I, Bilo L, Buti D, Casellato S, Cuccurullo C, Ferlazzo E, Leu C, Giordano L, Gobbi G, Hernandez-Hernandez L, Lench N, Martins H, Meletti S, Messana T, Nigro V, Pinelli M, Pippucci T, Bellampalli R, Salis B, Sofia V, Striano P, Striano S, Tassi L, Vignoli A, Vaudano AE, Viri M, Scheffer IE, May P, Zara F, Sisodiya SM.
    Epilepsia; 2024 Mar; 65(3):779-791. PubMed ID: 38088023
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  • 4. Candidate Genes for Eyelid Myoclonia with Absences, Review of the Literature.
    Mayo S, Gómez-Manjón I, Fernández-Martínez FJ, Camacho A, Martínez F, Benito-León J.
    Int J Mol Sci; 2021 May 25; 22(11):. PubMed ID: 34070602
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  • 6. Exacerbation of eyelid myoclonia in patients with epilepsy and eyelid myoclonia receiving cannabidiol.
    Zawar I, Franic L, Kotagal P, Knight EP.
    Epileptic Disord; 2021 Dec 01; 23(6):906-910. PubMed ID: 34642157
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  • 7. Clinical presentation and evaluation of epilepsy with eyelid myoclonia: Results of an international expert consensus panel.
    Smith KM, Wirrell EC, Andrade DM, Choi H, Trenité DK, Jones H, Knupp KG, Mugar J, Nordli DR, Riva A, Stern JM, Striano P, Thiele EA, Zawar I.
    Epilepsia; 2023 Sep 01; 64(9):2330-2341. PubMed ID: 37329145
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  • 9. Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases.
    von Stülpnagel C, Hartlieb T, Borggräfe I, Coppola A, Gennaro E, Eschermann K, Kiwull L, Kluger F, Krois I, Møller RS, Rössler F, Santulli L, Schwermer C, Wallacher-Scholz B, Zara F, Wolf P, Kluger G.
    Seizure; 2019 Feb 01; 65():131-137. PubMed ID: 30685520
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  • 10. Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia.
    Cerulli Irelli E, Cocchi E, Ramantani G, Morano A, Riva A, Caraballo RH, Giuliano L, Yilmaz T, Panagiotakaki E, Operto FF, Giraldez BG, Balestrini S, Silvennoinen K, Casciato S, Comajuan M, Fortunato F, Giallonardo AT, Gamirova R, Coppola A, Di Gennaro G, Labate A, Sofia V, Kluger GJ, Gambardella A, Kasteleijn-Nolst Trenite D, Baykan B, Sisodiya SM, Arzimanoglou A, Striano P, Di Bonaventura C, EEM Study Group.
    Epilepsia; 2023 Jun 01; 64(6):e105-e111. PubMed ID: 37021337
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  • 12. An Overview of the Electroencephalographic (EEG) Features of Epilepsy with Eyelid Myoclonia (Jeavons Syndrome).
    Zawar I, Pestana Knight EM.
    Neurodiagn J; 2020 Jun 01; 60(2):113-127. PubMed ID: 32369428
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  • 13. Eyelid myoclonia with absences related to epileptic negative myoclonus.
    Daida A, Yokoyama M, Yamamoto K, Hasegawa D, Kusakawa I, Wang CY, Ogihara M.
    Epileptic Disord; 2021 Dec 01; 23(6):917-921. PubMed ID: 34668865
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  • 15. Eyelid myoclonia seizures in adults: An alternate look at the syndrome paradox.
    Nar Senol P, Tezer FI, Saygi S.
    Epilepsy Behav; 2015 Apr 01; 45():265-70. PubMed ID: 25819946
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  • 16. The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study.
    Cerulli Irelli E, Cocchi E, Ramantani G, Riva A, Caraballo RH, Morano A, Giuliano L, Yilmaz T, Panagiotakaki E, Operto FF, Giraldez BG, Balestrini S, Silvennoinen K, Casciato S, Comajuan M, Fortunato F, Giallonardo AT, Gamirova R, Coppola A, Di Gennaro G, Labate A, Sofia V, Kluger GJ, Gambardella A, Kasteleijn-Nolst Trenite D, Baykan B, Sisodiya SM, Arzimanoglou A, Striano P, Di Bonaventura C, EMA study group.
    Epilepsia; 2022 Oct 28. PubMed ID: 36307934
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  • 17. Eyelid myoclonia with absences, intellectual disability and attention deficit hyperactivity disorder: a clinical phenotype of the RORB gene mutation.
    Morea A, Boero G, Demaio V, Francavilla T, La Neve A.
    Neurol Sci; 2021 May 28; 42(5):2059-2062. PubMed ID: 33387058
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  • 18. Novel NEXMIF gene pathogenic variant in a female patient with refractory epilepsy and intellectual disability.
    Wu D, Ji C, Chen Z, Wang K.
    Am J Med Genet A; 2020 Nov 28; 182(11):2765-2772. PubMed ID: 32924309
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  • 19. Jeavons syndrome in China.
    Wang XL, Bao JX, Liang-Shi, Tie-Ma, Deng YC, Zhao G, Swa B, Liu YH.
    Epilepsy Behav; 2014 Mar 28; 32():64-71. PubMed ID: 24495864
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  • 20. Abnormal visual sensitivity in eyelid myoclonia with absences: Evidence from electrocortical connectivity and non-linear quantitative analysis of EEG signal.
    Giuliano L, Mostile G, Fatuzzo D, Mainieri G, Nicoletti A, Sofia V, Zappia M.
    Seizure; 2019 Jul 28; 69():118-124. PubMed ID: 31015102
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