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Journal Abstract Search

109 related items for PubMed ID: 4184168

  • 61. [Myoclonic dystonia].
    Cassim F.
    Rev Neurol (Paris); 2003 Oct; 159(10 Pt 1):892-9. PubMed ID: 14615678
    [Abstract] [Full Text] [Related]

  • 62. [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; 56(6):509-13. PubMed ID: 15328840
    [Abstract] [Full Text] [Related]

  • 63.
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  • 64. Cutaneous findings in Unverricht's syndrome. (Progressive familial myoclonic epilepsy).
    Medved A, Peterson WC, Johnson RV.
    Arch Dermatol; 1967 Feb; 95(2):206-9. PubMed ID: 4225252
    [No Abstract] [Full Text] [Related]

  • 65.
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  • 66. Physiopathological observations on the mechanism of stimulus sensitive myoclonus. A stereotactic study.
    Cabrini GP, Marossero F, Ettorre G, Infuso L.
    Confin Neurol; 1972 Feb; 34(1):64-9. PubMed ID: 5084392
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  • 67.
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  • 68. [Electromyographic findings in myoclonus].
    Schenck E.
    Psychiatr Neurol Med Psychol Beih; 1969 Feb; 10-11():131-9. PubMed ID: 5006330
    [No Abstract] [Full Text] [Related]

  • 69.
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  • 72. Benign neonatal sleep myoclonus: case report and follow-up of four members of an affected family.
    Vaccario ML, Valenti MA, Carullo A, Di Bartolomeo R, Mazza S.
    Clin Electroencephalogr; 2003 Jan; 34(1):15-7. PubMed ID: 12515447
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  • 73.
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  • 74. Lafora body disease. Report of a family.
    Kumar BR, Rao NS, Banerjee AK, Chopra JS.
    Neurol India; 1975 Dec; 23(4):196-201. PubMed ID: 1219498
    [No Abstract] [Full Text] [Related]

  • 75. [Electroencephalogram in myoclonus epilepsy of Unverricht].
    GONZALEZ PEON VJ.
    Medicina (Madr); 1956 Jan; 24(1):5-16. PubMed ID: 13321301
    [No Abstract] [Full Text] [Related]

  • 76. [Progressive myoclonic epilepsy. Clinical, polygraphic and histopathological aspects of a case].
    Sanvito WL, Brandt RA, Gonzales DM, Tilbery CP, Stecca J.
    Arq Neuropsiquiatr; 1973 Jun; 31(2):123-31. PubMed ID: 4352862
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  • 77.
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  • 78. [Familial progressive myoclonic epilepsy (Unverricht-Lundborg syndrome in five Valaisian families). A contribution to the research of its metabolic origin through the study of urinary excretion of mucopolysaccharides].
    Rallo E.
    Acta Genet Med Gemellol (Roma); 1969 Jul; 18(3):231-70. PubMed ID: 4249667
    [No Abstract] [Full Text] [Related]

  • 79. Screening of mutations in NOL3 in a myoclonic syndromes series.
    Macerollo A, Mencacci NE, Erro R, Cordivari C, Edwards MJ, Wood NW, Bhatia KP.
    J Neurol; 2014 Sep; 261(9):1830-1. PubMed ID: 25138476
    [No Abstract] [Full Text] [Related]

  • 80. [Some observations from the study of evoked potentials in myoclonus epilepsy].
    Halliday AM.
    Bratisl Lek Listy; 1965 Sep 30; 45(6):357-66. PubMed ID: 5842772
    [No Abstract] [Full Text] [Related]

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