Cavum septi pellucidi, cavum vergae and cavum veli interpositi

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F20%3AA21025ZD" target="_blank" >RIV/61988987:17110/20:A21025ZD - isvavai.cz</a>
Result on the web
<a href="https://www.csnn.eu/en/journals/czech-and-slovak-neurology-and-neurosurgery/2020-2-3/cavum-septi-pellucidi-cavum-vergae-and-cavum-veli-interpositi-121847" target="_blank" >https://www.csnn.eu/en/journals/czech-and-slovak-neurology-and-neurosurgery/2020-2-3/cavum-septi-pellucidi-cavum-vergae-and-cavum-veli-interpositi-121847</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.14735/amcsnn2020166" target="_blank" >10.14735/amcsnn2020166</a>

Result language
angličtina
Original language name
Cavum septi pellucidi, cavum vergae and cavum veli interpositi
Original language description
Cavum septi pellucidi, cavum vergae and cavum veli interpositi are anterior midline intracranial findings which are typically incidental and are usually developmentally obliterated during postnatal life. Symptomatic and abnormally expanded cavities that do not have free communication with the lateral ventricles are called cysts. This review focuses on the embryology, anatomy, epidemiology, clinical symptomatology, radiological findings and treatment of these rare conditions.
Czech name
—
Czech description
—

Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
30212 - Surgery

Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2020
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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