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Journal Abstract Search

266 related items for PubMed ID: 28126647

  • 1. Movement-activated cortical myoclonus in Dravet syndrome.
    Canafoglia L, Ragona F, Panzica F, Piazza E, Freri E, Binelli S, Scaioli V, Avanzini G, Granata T, Franceschetti S.
    Epilepsy Res; 2017 Feb; 130():47-52. PubMed ID: 28126647
    [Abstract] [Full Text] [Related]

  • 2. A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data.
    Kobayashi Y, Hanaoka Y, Akiayma T, Ohmori I, Ouchida M, Yamamoto T, Oka M, Yoshinaga H, Kobayashi K.
    Brain Dev; 2017 Jan; 39(1):75-79. PubMed ID: 27523882
    [Abstract] [Full Text] [Related]

  • 3. [Polyneuro-electrophysiological studies of myoclonus in children].
    Wang B, Cai FC.
    Zhonghua Er Ke Za Zhi; 2009 Oct; 47(10):750-6. PubMed ID: 20021809
    [Abstract] [Full Text] [Related]

  • 4. Cortical myoclonus in childhood and juvenile onset Huntington's disease.
    Rossi Sebastiano D, Soliveri P, Panzica F, Moroni I, Gellera C, Gilioli I, Nardocci N, Ciano C, Albanese A, Franceschetti S, Canafoglia L.
    Parkinsonism Relat Disord; 2012 Jul; 18(6):794-7. PubMed ID: 22494662
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations.
    Rubboli G, Franceschetti S, Berkovic SF, Canafoglia L, Gambardella A, Dibbens LM, Riguzzi P, Campieri C, Magaudda A, Tassinari CA, Michelucci R.
    Epilepsia; 2011 Dec; 52(12):2356-63. PubMed ID: 22050460
    [Abstract] [Full Text] [Related]

  • 7. Focal subcortical reflex myoclonus. A clinical and neurophysiological study.
    Cantello R, Gianelli M, Civardi C, Mutani R.
    Arch Neurol; 1997 Feb; 54(2):187-96. PubMed ID: 9041860
    [Abstract] [Full Text] [Related]

  • 8. The spectrum of cortical myoclonus. From focal reflex jerks to spontaneous motor epilepsy.
    Obeso JA, Rothwell JC, Marsden CD.
    Brain; 1985 Mar; 108 ( Pt 1)():193-24. PubMed ID: 3919883
    [Abstract] [Full Text] [Related]

  • 9. Electroencephalographic features of patients with SCN1A-positive Dravet syndrome.
    Lee HF, Chi CS, Tsai CR, Chen CH, Wang CC.
    Brain Dev; 2015 Jun; 37(6):599-611. PubMed ID: 25459968
    [Abstract] [Full Text] [Related]

  • 10. Dravet syndrome: a genetic epileptic disorder.
    Akiyama M, Kobayashi K, Ohtsuka Y.
    Acta Med Okayama; 2012 Jun; 66(5):369-76. PubMed ID: 23093055
    [Abstract] [Full Text] [Related]

  • 11. Dravet syndrome, what is new?
    Al-Baradie RS.
    Neurosciences (Riyadh); 2013 Jan; 18(1):11-7. PubMed ID: 23291792
    [Abstract] [Full Text] [Related]

  • 12. From focal epilepsy to Dravet syndrome--Heterogeneity of the phenotype due to SCN1A mutations of the p.Arg1596 amino acid residue in the Nav1.1 subunit.
    Hoffman-Zacharska D, Szczepanik E, Terczynska I, Goszczanska-Ciuchta A, Zalewska-Miszkurka Z, Tataj R, Bal J.
    Neurol Neurochir Pol; 2015 Jan; 49(4):258-66. PubMed ID: 26188943
    [Abstract] [Full Text] [Related]

  • 13. On the significance of giant somatosensory evoked potentials in cortical myoclonus.
    Rothwell JC, Obeso JA, Marsden CD.
    J Neurol Neurosurg Psychiatry; 1984 Jan; 47(1):33-42. PubMed ID: 6420519
    [Abstract] [Full Text] [Related]

  • 14. Sleep abnormalities in children with Dravet syndrome.
    Dhamija R, Erickson MK, St Louis EK, Wirrell E, Kotagal S.
    Pediatr Neurol; 2014 May; 50(5):474-8. PubMed ID: 24656210
    [Abstract] [Full Text] [Related]

  • 15. Coherence analysis in the myoclonus of corticobasal degeneration.
    Grosse P, Kühn A, Cordivari C, Brown P.
    Mov Disord; 2003 Nov; 18(11):1345-50. PubMed ID: 14639679
    [Abstract] [Full Text] [Related]

  • 16. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
    Lim BC, Hwang H, Kim H, Chae JH, Choi J, Kim KJ, Hwang YS, Yum MS, Ko TS.
    Epilepsy Res; 2015 Jan; 109():34-9. PubMed ID: 25524840
    [Abstract] [Full Text] [Related]

  • 17. Motor neuropathy contributes to crouching in patients with Dravet syndrome.
    Gitiaux C, Chemaly N, Quijano-Roy S, Barnerias C, Desguerre I, Hully M, Chiron C, Dulac O, Nabbout R.
    Neurology; 2016 Jul 19; 87(3):277-81. PubMed ID: 27316242
    [Abstract] [Full Text] [Related]

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  • 20. Convulsive seizures and some behavioral comorbidities are uncoupled in the Scn1aA1783V Dravet syndrome mouse model.
    Fadila S, Quinn S, Turchetti Maia A, Yakubovich D, Ovadia M, Anderson KL, Giladi M, Rubinstein M.
    Epilepsia; 2020 Oct 19; 61(10):2289-2300. PubMed ID: 32865826
    [Abstract] [Full Text] [Related]

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