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Autoimmune and limbic encephalitis: case series with some atypical variables in clinical practice

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F22%3A00075987" target="_blank" >RIV/65269705:_____/22:00075987 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14110/22:00125087

  • Result on the web

    <a href="https://link.springer.com/article/10.1007/s10072-021-05563-x" target="_blank" >https://link.springer.com/article/10.1007/s10072-021-05563-x</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s10072-021-05563-x" target="_blank" >10.1007/s10072-021-05563-x</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Autoimmune and limbic encephalitis: case series with some atypical variables in clinical practice

  • Original language description

    Autoimmune and limbic encephalitides are still rare diseases characterized by rapid diagnostics and treatment development in recent years. The incidence of anti-N-methyl-D- aspartate receptor [NMDAR] encephalitis is about 1.5 per million person per year, and the incidence of paraneoplastic neurological syndromes [PNS] including limbic encephalitis [LE] is about 1.22 per 100 000 person per year (Vogrig et al. J Neurol 267:26-35, 1; Dalmau et al. Ann Neurol 61:25-36, 2). The diagnostic criteria of anti-NMDAR encephalitis are already well established (Zuliani et al. Neurol Sci 40:2017-2030, 10). We provide immunological and clinical characteristics of anti-NMDAR encephalitis case series emphasizing unusual association with colon tumour in one case and complete recovery in two cases. Then we report two cases of onconeural and cell surface antibody negative limbic encephalitis [LE] associated with tumours, seizures, cognitive and behavioural changes resulting in severe cerebellar syndrome and fatal outcome. The clinical characteristics and results of selected paraclinical examinations as electroencephalography [EEG], magnetic resonance imaging [MRI] and cerebrospinal fluid [CSF] analysis are reviewed.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30210 - Clinical neurology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Neurological Sciences

  • ISSN

    1590-1874

  • e-ISSN

    1590-3478

  • Volume of the periodical

    43

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    IT - ITALY

  • Number of pages

    4

  • Pages from-to

    687-690

  • UT code for WoS article

    000687902800001

  • EID of the result in the Scopus database

    2-s2.0-85113315851