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Journal Abstract Search

322 related items for PubMed ID: 23205932

  • 1. Family studies of individuals with eyelid myoclonia with absences.
    Sadleir LG, Vears D, Regan B, Redshaw N, Bleasel A, Scheffer IE.
    Epilepsia; 2012 Dec; 53(12):2141-8. PubMed ID: 23205932
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  • 3. 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; 54(2):280-7. PubMed ID: 23294109
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  • 9. New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p.
    Nabbout R, Baulac S, Desguerre I, Bahi-Buisson N, Chiron C, Ruberg M, Dulac O, LeGuern E.
    Neurology; 2007 Apr 24; 68(17):1374-81. PubMed ID: 17452582
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  • 10. Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes.
    Vears DF, Tsai MH, Sadleir LG, Grinton BE, Lillywhite LM, Carney PW, Harvey AS, Berkovic SF, Scheffer IE.
    Epilepsia; 2012 Feb 24; 53(2):319-24. PubMed ID: 22220564
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  • 14. Childhood Absence Epilepsy evolving to Eyelid Myoclonia with Absence Epilepsy.
    Galli J, Micheletti S, Malerba L, Fazzi E, Giordano L.
    Seizure; 2018 Oct 24; 61():1-3. PubMed ID: 30029089
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  • 15. Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation.
    Marini C, Harkin LA, Wallace RH, Mulley JC, Scheffer IE, Berkovic SF.
    Brain; 2003 Jan 24; 126(Pt 1):230-40. PubMed ID: 12477709
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  • 16. Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences.
    Cerulli Irelli E, Cocchi E, Ramantani G, Caraballo RH, Giuliano L, Yilmaz T, Morano A, Panagiotakaki E, Operto FF, Gonzalez Giraldez B, Silvennoinen K, Casciato S, Comajuan M, Balestrini S, Fortunato F, Coppola A, Di Gennaro G, Labate A, Sofia V, Kluger GJ, Kasteleijn-Nolst Trenité DGA, Gambardella A, Baykan B, Sisodiya SM, Arzimanoglou A, Striano P, Di Bonaventura C, EMA Study Group.
    Neurology; 2022 May 03; 98(18):e1865-e1876. PubMed ID: 35292555
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  • 18. Eyelid myoclonia seizures in adults: An alternate look at the syndrome paradox.
    Nar Senol P, Tezer FI, Saygi S.
    Epilepsy Behav; 2015 Apr 03; 45():265-70. PubMed ID: 25819946
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  • 20. [Idiopathic absence epilepsy].
    Szczepanik E, Pakszys M.
    Przegl Lek; 2001 Apr 03; 58 Suppl 1():32-6. PubMed ID: 11355107
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