VEXAS syndrome: a report of three cases
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F22%3A00013413" target="_blank" >RIV/00023736:_____/22:00013413 - isvavai.cz</a>
Result on the web
<a href="https://doi.org/10.55563/clinexprheumatol/3z07e9" target="_blank" >https://doi.org/10.55563/clinexprheumatol/3z07e9</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.55563/clinexprheumatol/3z07e9" target="_blank" >10.55563/clinexprheumatol/3z07e9</a>
Alternative languages
Result language
angličtina
Original language name
VEXAS syndrome: a report of three cases
Original language description
The recently described VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) presents as a late adult-onset autoinflammatory disease often accompanied by haematological manifestations.
Czech name
—
Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30205 - Hematology
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Clinical and experimental rheumatology
ISSN
0392-856X
e-ISSN
—
Volume of the periodical
40
Issue of the periodical within the volume
7
Country of publishing house
IT - ITALY
Number of pages
1
Pages from-to
1449
UT code for WoS article
000904975700028
EID of the result in the Scopus database
2-s2.0-85134270249