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Current Concepts in the Classification and Diagnosis of Frontotemporal Lobar Degenerations A Practical Approach

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F14%3A43907956" target="_blank" >RIV/00216208:11120/14:43907956 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064190:_____/14:#0000825

  • Result on the web

    <a href="http://dx.doi.org/10.5858/arpa.2012-0510-RS" target="_blank" >http://dx.doi.org/10.5858/arpa.2012-0510-RS</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.5858/arpa.2012-0510-RS" target="_blank" >10.5858/arpa.2012-0510-RS</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Current Concepts in the Classification and Diagnosis of Frontotemporal Lobar Degenerations A Practical Approach

  • Original language description

    Frontotemporal lobar degenerations are clinically, genetically, and molecularly heterogeneous diseases characterized by mainly frontal and temporal atrophy and affecting behavioral, language, cognitive, and motor functions. The term frontotemporal dementia incorporates 3 distinct clinical syndromes seen in frontotemporal degenerations: behavioral variant of frontotemporal dementia, progressive nonfluent aphasia, and semantic dementia. Progressive supranuclear palsy syndrome, corticobasal syndrome, and motor neuron disease syndrome are also associated with frontotemporal lobar degenerations. The neuropathologic hallmark of frontotemporal lobar degenerations is accumulation of abnormal proteins in the cytoplasm and nuclei of neurons and glial cells. Proteins involved in pathologic processes that represent the basis for frontotemporal lobar degeneration classification are tau protein, transactive response DNA-binding protein of 43 kDa, and "fused in sarcoma" protein. The aim of this revie

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NT12094" target="_blank" >NT12094: Multidisciplinary approach in the diagnosis of frontotemporal lobar degenerations and tauopathies: new insights into pathogenetic mechanisms</a><br>

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Archives of Pathology & Laboratory Medicine

  • ISSN

    0003-9985

  • e-ISSN

  • Volume of the periodical

    138

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

    132-138

  • UT code for WoS article

    000339549400020

  • EID of the result in the Scopus database