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Journal Abstract Search

266 related items for PubMed ID: 27523882

  • 21.
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  • 23. [Clinical and polyneuroelectrophysiological characteristics of infantile spasm].
    Wang B, Cai FC.
    Zhonghua Er Ke Za Zhi; 2007 Feb; 45(2):109-14. PubMed ID: 17456338
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  • 24. Familial cortical myoclonic tremor as a unique form of cortical reflex myoclonus.
    Terada K, Ikeda A, Mima T, Kimura M, Nagahama Y, Kamioka Y, Murone I, Kimura J, Shibasaki H.
    Mov Disord; 1997 May; 12(3):370-7. PubMed ID: 9159732
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  • 25. Cortical tremor (FCMTE: familial cortical myoclonic tremor with epilepsy).
    Regragui W, Gerdelat-Mas A, Simonetta-Moreau M.
    Neurophysiol Clin; 2006 May; 36(5-6):345-9. PubMed ID: 17336780
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  • 28. Presence of Bereitschaftspotential preceding psychogenic myoclonus: clinical application of jerk-locked back averaging.
    Terada K, Ikeda A, Van Ness PC, Nagamine T, Kaji R, Kimura J, Shibasaki H.
    J Neurol Neurosurg Psychiatry; 1995 Jun; 58(6):745-7. PubMed ID: 7608681
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  • 29. [A case of cortical reflex myoclonus manifesting tremor].
    Takigawa T, Mima T, Saida K, Kawasaki J, Shibasaki H.
    Rinsho Shinkeigaku; 1997 Nov; 37(11):1006-9. PubMed ID: 9503972
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  • 30. Dravet syndrome--considerable delay in making the diagnosis.
    Bremer A, Lossius MI, Nakken KO.
    Acta Neurol Scand; 2012 May; 125(5):359-62. PubMed ID: 22050316
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  • 31. Variability of EEG-fMRI findings in patients with SCN1A-positive Dravet syndrome.
    Moehring J, von Spiczak S, Moeller F, Helbig I, Wolff S, Jansen O, Muhle H, Boor R, Stephani U, Siniatchkin M.
    Epilepsia; 2013 May; 54(5):918-26. PubMed ID: 23398550
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  • 33. Vaccination and occurrence of seizures in SCN1A mutation-positive patients: a multicenter Italian study.
    Zamponi N, Passamonti C, Petrelli C, Veggiotti P, Baldassari C, Verrotti A, Capovilla G, Viri M, Coppola G, Vignoli A.
    Pediatr Neurol; 2014 Mar; 50(3):228-32. PubMed ID: 24405698
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  • 34. Periodic synchronous discharge and myoclonus in Creutzfeldt-Jakob disease: diagnostic application of jerk-locked averaging method.
    Shibasaki H, Motomura S, Yamashita Y, Shii H, Kuroiwa Y.
    Ann Neurol; 1981 Feb; 9(2):150-6. PubMed ID: 7015993
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  • 35. Ictal ontogeny in Dravet syndrome.
    Kim SH, Nordli DR, Berg AT, Koh S, Laux L.
    Clin Neurophysiol; 2015 Mar; 126(3):446-55. PubMed ID: 25046982
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  • 37. Not everything that shakes is a seizure… Role of continuous EEG in the intensive care unit.
    Ritzenthaler T, Laurencin C, André Obadia N, Bodonian C, Dailler F.
    Neurophysiol Clin; 2017 Feb; 47(1):13-18. PubMed ID: 27856078
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  • 38. Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French family.
    Magnin E, Vidailhet M, Depienne C, Saint-Martin C, Bouteiller D, LeGuern E, Apartis E, Rumbach L, Labauge P.
    Rev Neurol (Paris); 2009 Oct; 165(10):812-20. PubMed ID: 19616813
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  • 39. Generalized periodic epileptiform discharges in a child with Dravet syndrome.
    Moseley BD, Wirrell EC, Nickels K.
    J Child Neurol; 2011 Jul; 26(7):907-10. PubMed ID: 21335542
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  • 40. High-frequency rhythmic cortical myoclonus in a long-surviving patient with nonketotic hypergylcemia.
    Mastrangelo M, Canafoglia L, Franceschetti S, Oppezzo C, Mosca F, Menni F, Parini R, Ciano C, Scaioli V, Panzica F.
    J Child Neurol; 2008 Mar; 23(3):321-4. PubMed ID: 18182648
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