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

Kód výsledku v 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>

Nalezeny alternativní kódy

RIV/00064190:_____/14:#0000825

Výsledek na webu

<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>

Jazyk výsledku

angličtina

Název v původním jazyce

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

Popis výsledku v původním jazyce

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

Název v anglickém jazyce

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

Popis výsledku anglicky

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

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FD - Onkologie a hematologie

OECD FORD obor

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Projekt

<a href="/cs/project/NT12094" target="_blank" >NT12094: Multidisciplinární přístup v diagnostice frontotemporálních lobárních degenerací a tauopatií: komplexní pohled na patogenetické mechanismy</a><br>

Návaznosti

S - Specificky vyzkum na vysokych skolach

Rok uplatnění

2014

Kód důvěrnosti údajů

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

Název periodika

Archives of Pathology & Laboratory Medicine

ISSN

0003-9985

e-ISSN

—

Svazek periodika

138

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

7

Strana od-do

132-138

Kód UT WoS článku

000339549400020

EID výsledku v databázi Scopus

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