Mid-aortic syndrome with renovascular hypertension and multisytem involvement in a girl with familiar neurofibromatosis von Recklinghausen type 1
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F07%3A1510" target="_blank" >RIV/00064203:_____/07:1510 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11130/07:1510
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Mid-aortic syndrome with renovascular hypertension and multisytem involvement in a girl with familiar neurofibromatosis von Recklinghausen type 1
Original language description
Neurofibromatosis von Recklinghausen type I (NF1) is an autosomal dominant neurocutaneous disorder affecting one in 3000-4000 individuals.
Czech name
Mid-aortický syndrom s revaskulární hypertenzí
Czech description
Neurofibromatóza
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FH - Neurology, neuro-surgery, nuero-sciences
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2007
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Neuroendocrinology letters
ISSN
0172-780X
e-ISSN
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Volume of the periodical
28
Issue of the periodical within the volume
6
Country of publishing house
SE - SWEDEN
Number of pages
5
Pages from-to
734-738
UT code for WoS article
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EID of the result in the Scopus database
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