Hereditary Renal Hypouricemia: A New Role for Allopurinol?
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F14%3A10285461" target="_blank" >RIV/00216208:11110/14:10285461 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1016/j.amjmed.2013.08.025" target="_blank" >http://dx.doi.org/10.1016/j.amjmed.2013.08.025</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.amjmed.2013.08.025" target="_blank" >10.1016/j.amjmed.2013.08.025</a>
Alternative languages
Result language
angličtina
Original language name
Hereditary Renal Hypouricemia: A New Role for Allopurinol?
Original language description
Hereditary renal hypouricemia is a genetic disorder characterized by defective renal handling of uric acid. The affected individuals are predisposed to recurrent episodes of exercise-induced non-myoglobinuric acute kidney injury and nephrolithiasis.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FB - Endocrinology, diabetology, metabolism, nutrition
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>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2014
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 Medicine
ISSN
0002-9343
e-ISSN
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Volume of the periodical
127
Issue of the periodical within the volume
1
Country of publishing house
US - UNITED STATES
Number of pages
2
Pages from-to
"E3"-"E4"
UT code for WoS article
000329125300002
EID of the result in the Scopus database
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