Search Results - "Vachalová, I."

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    Anti-GM2, -GD1a and -GD1b positive purely isolated facial diplegia by Vachalová, I, Golden, V, Heckmann, J.G

    Published in Clinical neurology and neurosurgery (01-07-2014)
    “…First the clinical finding of purely isolated facial diplegia with pronounced GBS-typical CSF composition is quite unique. [...]purely isolated facial diplegia…”
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    Journal Article
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    Adrenoleukodystrophy--a new mutation identified by Vachalova, I, Chandoga, J, Petrovic, R, Copikova-Cudrakova, D, Sykora, M, Traubner, P

    Published in Bratislavské lékarské listy (2007)
    “…X-linked adrenoleukodystrophy from the group of peroxisomal disorders presents with an extensive spectrum of phenotypes. The mutation affects the ABCD1 gene…”
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    Solitary epileptic seizures in the clinical practice. Part I: etiological factors responsible for their occurrence by Martiniskova, Zuzana, Kollar, Branislav, Vachalova, Ivana, Klobucnikova, Katarína, Waczulikova, Iveta, Goldenberg, Zoltan

    Published in Neuro-endocrinology letters (2009)
    “…Approximately 5% of the general population experiences at least one unprovoked epileptic seizure in the lifetime. This is in contrast to the cumulative…”
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