Dendritic cell neurofibroma with pseudorosettes lacks mutations in Exons 1-15 of the neurofibromatosis type 2 gene
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F05%3A00000758" target="_blank" >RIV/00216208:11140/05:00000758 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Dendritic cell neurofibroma with pseudorosettes lacks mutations in Exons 1-15 of the neurofibromatosis type 2 gene
Original language description
Dendritic cell neurofibroma with pseudorosettes is a recently proposed variant of neurofibroma with a distinctive microscopic appearance that is produced by a pseudorosette pattern formed by small, dark, lymphocyte-like cells concentrically around larger.
Czech name
Dendritický neurofibrom spseudorosetami postrádá mutace exonu 1-15 genu 2 pro neurofibromatozu
Czech description
Dendritický neurofibrom spseudorosetami postrádá mutace exonu 1-15 genu 2 pro neurofibromatozu.
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FP - Other medical fields
OECD FORD branch
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Result continuities
Project
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Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2005
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
American Journal of Dermatopathology
ISSN
0193-1091
e-ISSN
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Volume of the periodical
27
Issue of the periodical within the volume
4
Country of publishing house
US - UNITED STATES
Number of pages
4
Pages from-to
286-289
UT code for WoS article
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EID of the result in the Scopus database
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