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Pyramidal system involvement in progressive supranuclear palsy - a clinicopathological correlation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023752%3A_____%2F19%3A43919828" target="_blank" >RIV/00023752:_____/19:43919828 - isvavai.cz</a>

  • Alternative codes found

    RIV/68407700:21340/19:00335995 RIV/00216208:11110/19:10392928 RIV/00216208:11120/19:43917826 RIV/00064173:_____/19:N0000014 and 2 more

  • Result on the web

    <a href="https://bmcneurol.biomedcentral.com/articles/10.1186/s12883-019-1270-1#Abs1" target="_blank" >https://bmcneurol.biomedcentral.com/articles/10.1186/s12883-019-1270-1#Abs1</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1186/s12883-019-1270-1" target="_blank" >10.1186/s12883-019-1270-1</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Pyramidal system involvement in progressive supranuclear palsy - a clinicopathological correlation

  • Original language description

    Background: We aimed to produce a detailed neuropathological analysis of pyramidal motor system pathology and provide its clinical pathological correlation in cases with definite progressive supranuclear palsy (PSP). Methods: Pyramidal motor system pathologies were analyzed in 18 cases with neuropathologically confirmed PSP. Based on a retrospective clinical analysis, cases were subtyped according to Movement Disorder Society criteria for clinical diagnosis of PSP as probable, possible or suggestive of PSP with Richardson’s syndrome (n = 10), PSP with predominant corticobasal syndrome (n = 3), PSP with predominant parkinsonism (n = 3), PSP with predominant speech/language disorder (n = 1), and PSP with progressive gait freezing (n = 1). Clinical manifestations of motor neuron involvement (pseudobulbar or bulbar signs and spasticity) were retrospectively assessed semiquantitatively. Neuropathologically, hyperphosphorylated tau-related pyramidal motor system neuronal, neuritic, and glial pathology using anti-tau AT8 clone immunohistochemistry, was also evaluated. Results: Clinical manifestations of pyramidal motor system involvement were found in patients with different PSP subtypes. A statistically significant higher load of tau pathology was found in the pyramidal system in PSP-Richardson’s syndrome compared to other PSP subtypes (p = 0.016); however, there was no significant correlation between pyramidal system tau pathology and related motor clinical symptoms. Conclusions: Tau pathology in the spinal cord and pyramidal motor system structures is very common in progressive supranuclear palsy and may neuropathologically supplement the distinction between classic Richardson’s syndrome from other progressive supranuclear palsy subtypes.

  • 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

    <a href="/en/project/LO1611" target="_blank" >LO1611: Sustainability for The National Institute of Mental Health</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2019

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    BMC Neurology

  • ISSN

    1471-2377

  • e-ISSN

  • Volume of the periodical

    19

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    "Article number 42"

  • UT code for WoS article

    000462234800001

  • EID of the result in the Scopus database

    2-s2.0-85063275822