All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Corpus callosum hypersignals and focal atrophy: Neuroimaging findings in globular glial tauopathy type I

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064190%3A_____%2F21%3AN0000025" target="_blank" >RIV/00064190:_____/21:N0000025 - isvavai.cz</a>

  • Alternative codes found

    RIV/00023884:_____/21:00008959 RIV/00216208:11120/22:43922029 RIV/00064190:_____/22:N0000129

  • Result on the web

    <a href="http://dx.doi.org/10.1111/ene.15090" target="_blank" >http://dx.doi.org/10.1111/ene.15090</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1111/ene.15090" target="_blank" >10.1111/ene.15090</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Corpus callosum hypersignals and focal atrophy: Neuroimaging findings in globular glial tauopathy type I

  • Original language description

    Background and purpose Globular glial tauopathies (GGTs) have heterogeneous presentations; little evidence regarding typical clinical and magnetic resonance imaging (MRI) presentations are available. Methods We retrospectively assessed MRIs from three postmortem-confirmed GGT cases, in two patients with atypical progressive aphasia and one with corticobasal syndrome. Results We suggest that four principal concomitant MRI findings characterize GGT type I: a sagittal callosal hyperintense band, marked focal callosal atrophy suggesting white matter degeneration originating in cortical areas responsible for symptoms (anterior atrophy in predominantly language manifestations and posterior atrophy in predominantly apraxia), periventricular white matter lesions, and mild-to-moderate brain stem atrophy. Conclusions We observed four concomitant MRI abnormalities in patients with atypical dementia, parkinsonism, and late incomplete supranuclear gaze palsy. Two patients had atypical progressive aphasia and one had corticobasal syndrome.

  • 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

    30103 - Neurosciences (including psychophysiology)

Result continuities

  • Project

    <a href="/en/project/NV19-04-00090" target="_blank" >NV19-04-00090: Overlap of neurodegenerative dementias and their clinic-pathological correlations: a prospective-retrospective multicentric study</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    EUROPEAN JOURNAL OF NEUROLOGY

  • ISSN

    1351-5101

  • e-ISSN

    1468-1331

  • Volume of the periodical

    29

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    5

  • Pages from-to

    324-328

  • UT code for WoS article

    000695089600001

  • EID of the result in the Scopus database

    2-s2.0-85114708278