Building a network of ADPKD reference centres across Europe: the EuroCYST initiative

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F14%3A10282531" target="_blank" >RIV/00216208:11110/14:10282531 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00064165:_____/14:10282531

Výsledek na webu

<a href="http://dx.doi.org/10.1093/ndt/gfu091" target="_blank" >http://dx.doi.org/10.1093/ndt/gfu091</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1093/ndt/gfu091" target="_blank" >10.1093/ndt/gfu091</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Building a network of ADPKD reference centres across Europe: the EuroCYST initiative

Popis výsledku v původním jazyce

Background. Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenic inherited kidney disease, affecting an estimated 600 000 individuals in Europe. The disease is characterized by age-dependent development of a multiple cysts inthe kidneys, ultimately leading to end-stage renal failure and the need of renal replacement therapy in the majority of patients, typically by the fifth or sixth decade of life. The variable disease course, even within the same family, remains largely unexplained. Similarly, assessing disease severity and prognosis in an individual with ADPKD remains difficult. Epidemiological studies are limited due to the fragmentation of ADPKD research in Europe. Methods. The EuroCYST initiative aims: (i) to harmonize and develop common standards for ADPKD research by starting a collaborative effort to build a network of ADPKD reference centres across Europe and (ii) to establish a multicentric observational cohort of ADPKD patients. This cohort wil

Název v anglickém jazyce

Building a network of ADPKD reference centres across Europe: the EuroCYST initiative

Popis výsledku anglicky

Background. Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenic inherited kidney disease, affecting an estimated 600 000 individuals in Europe. The disease is characterized by age-dependent development of a multiple cysts inthe kidneys, ultimately leading to end-stage renal failure and the need of renal replacement therapy in the majority of patients, typically by the fifth or sixth decade of life. The variable disease course, even within the same family, remains largely unexplained. Similarly, assessing disease severity and prognosis in an individual with ADPKD remains difficult. Epidemiological studies are limited due to the fragmentation of ADPKD research in Europe. Methods. The EuroCYST initiative aims: (i) to harmonize and develop common standards for ADPKD research by starting a collaborative effort to build a network of ADPKD reference centres across Europe and (ii) to establish a multicentric observational cohort of ADPKD patients. This cohort wil

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FE - Ostatní obory vnitřního lékařství

OECD FORD obor

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Projekt

—

Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2014

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Nephrology Dialysis Transplantation

ISSN

0931-0509

e-ISSN

—

Svazek periodika

29

Číslo periodika v rámci svazku

suppl.4

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

7

Strana od-do

26-32

Kód UT WoS článku

000342940300004

EID výsledku v databázi Scopus

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