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Journal Abstract Search

203 related items for PubMed ID: 21426326

  • 21. Primary generalized epilepsy with photosensitivity and seizures on awakening. Report of a family.
    Natale S, Mastroroberto G, Vacca G, De Falco FA, Bianchi L.
    Acta Neurol (Napoli); 1988; 10(4-5):262-8. PubMed ID: 3146213
    [No Abstract] [Full Text] [Related]

  • 22. Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy.
    Cen Z, Huang C, Yin H, Ding X, Xie F, Lu X, Ouyang Z, Lou Y, Qiu X, Wang Z, Xiao J, Ding M, Luo W.
    Mov Disord; 2016 Nov; 31(11):1704-1710. PubMed ID: 27613677
    [Abstract] [Full Text] [Related]

  • 23. Autosomal dominant cortical tremor, myoclonus and epilepsy.
    Striano P, Zara F.
    Epileptic Disord; 2016 Sep 01; 18(S2):139-144. PubMed ID: 27618961
    [Abstract] [Full Text] [Related]

  • 24. [A case of the familial essential myoclonus and epilepsy presenting behavioral arrest].
    Morita S, Miwa H, Kondo T.
    No To Shinkei; 2003 Apr 01; 55(4):345-8. PubMed ID: 12755039
    [Abstract] [Full Text] [Related]

  • 25. Logopenic syndrome and corticobasal dysfunction in a "benign" type 3 familial cortical myoclonic tremor with epilepsy.
    Magnin E.
    Seizure; 2015 Feb 01; 25():84-6. PubMed ID: 25645643
    [No Abstract] [Full Text] [Related]

  • 26. Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME) in a unique south Indian community.
    Mahadevan R, Viswanathan N, Shanmugam G, Sankaralingam S, Essaki B, Chelladurai RP.
    Epilepsia; 2016 Mar 01; 57(3):e56-9. PubMed ID: 26749494
    [Abstract] [Full Text] [Related]

  • 27. Genetics of myoclonic and myoclonus epilepsies.
    Minassian BA, Sainz J, Delgado-Escueta AV.
    Clin Neurosci; 2016 Mar 01; 3(4):223-35. PubMed ID: 8891396
    [Abstract] [Full Text] [Related]

  • 28. Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy.
    Di Bonaventura C, Operto FF, Busolin G, Egeo G, D'Aniello A, Vitello L, Smaniotto G, Furlan S, Diani E, Michelucci R, Giallonardo AT, Coppola G, Nobile C.
    Epilepsia; 2011 Jul 01; 52(7):1258-64. PubMed ID: 21504429
    [Abstract] [Full Text] [Related]

  • 29. [Recent advance in research of benign adult familial myoclonus epilepsy (BAFME): is BAFME a progressive disorder?].
    Hitomi T, Takahashi R, Ikeda A.
    Rinsho Shinkeigaku; 2014 Jul 01; 54(12):1142-5. PubMed ID: 25672731
    [Abstract] [Full Text] [Related]

  • 30. Familial adult onset myoclonic epilepsy associated with migraine.
    Saka E, Saygi S.
    Seizure; 2000 Jul 01; 9(5):344-6. PubMed ID: 10933990
    [Abstract] [Full Text] [Related]

  • 31. Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1.
    Cen Z, Jiang Z, Chen Y, Zheng X, Xie F, Yang X, Lu X, Ouyang Z, Wu H, Chen S, Yin H, Qiu X, Wang S, Ding M, Tang Y, Yu F, Li C, Wang T, Ishiura H, Tsuji S, Jiao C, Liu C, Xiao J, Luo W.
    Brain; 2018 Aug 01; 141(8):2280-2288. PubMed ID: 29939203
    [Abstract] [Full Text] [Related]

  • 32. [Familial progressive myoclonus epilepsy (Unverricht/Lundborg)].
    Herbst A.
    Psychiatr Neurol Med Psychol Beih; 1967 Aug 01; 6():18-39. PubMed ID: 5006319
    [No Abstract] [Full Text] [Related]

  • 33. [Seven families with heredofamilial tremor and epilepsy].
    Kudo J, Kudo T, Yamauchi T.
    Rinsho Shinkeigaku; 1984 Jan 01; 24(1):1-8. PubMed ID: 6467734
    [No Abstract] [Full Text] [Related]

  • 34. [A case of familial essential myoclonus and epilepsy with suspected focus in the hemisphere ipsilateral to myoclonus limbs].
    Asai H, Udaka F, Oishi N, Kubori T, Kameyama M.
    No To Shinkei; 2004 Jun 01; 56(6):509-13. PubMed ID: 15328840
    [Abstract] [Full Text] [Related]

  • 35. Clinical analysis in familial cortical myoclonic tremor allows differential diagnosis with essential tremor.
    Bourdain F, Apartis E, Trocello JM, Vidal JS, Masnou P, Vercueil L, Vidailhet M.
    Mov Disord; 2006 May 01; 21(5):599-608. PubMed ID: 16281296
    [Abstract] [Full Text] [Related]

  • 36. [A case of familial myoclonus showing extremely benign clinical course].
    Nagayama S, Kishikawa H, Yukitake M, Matsui M, Kuroda Y.
    Rinsho Shinkeigaku; 1998 May 01; 38(5):430-4. PubMed ID: 9805989
    [Abstract] [Full Text] [Related]

  • 37. Clinical evaluation and diagnosis of severe epilepsy syndromes of early childhood.
    Zupanc ML.
    J Child Neurol; 2009 Aug 01; 24(8 Suppl):6S-14S. PubMed ID: 19666878
    [Abstract] [Full Text] [Related]

  • 38. The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism.
    Martí-Massó JF, Bergareche A, Makarov V, Ruiz-Martinez J, Gorostidi A, López de Munain A, Poza JJ, Striano P, Buxbaum JD, Paisán-Ruiz C.
    J Mol Med (Berl); 2013 Dec 01; 91(12):1399-406. PubMed ID: 23955123
    [Abstract] [Full Text] [Related]

  • 39. Familial cortical myoclonic tremor with epilepsy: TTTCA/TTTTA repeat expansions and expanding phenotype in two Chinese families.
    Zhang Y, Xiong W, Lu L, Zhou D.
    Brain Res; 2020 Jun 15; 1737():146796. PubMed ID: 32194077
    [Abstract] [Full Text] [Related]

  • 40.
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    [No Abstract] [Full Text] [Related]

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