Paper 6: EUROCAT member registries: Organization and activities

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F11%3A00003567" target="_blank" >RIV/00216208:11120/11:00003567 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1002/bdra.20775" target="_blank" >http://dx.doi.org/10.1002/bdra.20775</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1002/bdra.20775" target="_blank" >10.1002/bdra.20775</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Paper 6: EUROCAT member registries: Organization and activities

Popis výsledku v původním jazyce

EUROCAT is a network of population-based congenital anomaly registries providing standardized epidemiologic information on congenital anomalies in Europe. There are three types of EUROCAT membership: full, associate, or affiliate. Full member registriessend individual records of all congenital anomalies covered by their region. Associate members transmit aggregate case counts for each EUROCAT anomaly subgroup by year and by type of birth. This article describes the organization and activities of each of the current 29 full member and 6 associate member registries of EUROCAT. Each registry description provides information on the history and funding of the registry, population coverage including any changes in coverage over time, sources for ascertaining cases of congenital anomalies, and upper age limit for registering cases of congenital anomalies. It also details the legal requirements relating to termination of pregnancy for fetal anomalies, the definition of stillbirths and fetal d

Název v anglickém jazyce

Paper 6: EUROCAT member registries: Organization and activities

Popis výsledku anglicky

EUROCAT is a network of population-based congenital anomaly registries providing standardized epidemiologic information on congenital anomalies in Europe. There are three types of EUROCAT membership: full, associate, or affiliate. Full member registriessend individual records of all congenital anomalies covered by their region. Associate members transmit aggregate case counts for each EUROCAT anomaly subgroup by year and by type of birth. This article describes the organization and activities of each of the current 29 full member and 6 associate member registries of EUROCAT. Each registry description provides information on the history and funding of the registry, population coverage including any changes in coverage over time, sources for ascertaining cases of congenital anomalies, and upper age limit for registering cases of congenital anomalies. It also details the legal requirements relating to termination of pregnancy for fetal anomalies, the definition of stillbirths and fetal d

Druh

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

CEP obor

FK - Gynekologie a porodnictví

OECD FORD obor

—

Projekt

—

Návaznosti

N - Vyzkumna aktivita podporovana z neverejnych zdroju

Rok uplatnění

2011

Kód důvěrnosti údajů

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

Název periodika

Birth Defects Research Part A - Clinical and Molecular Teratology

ISSN

1542-9768

e-ISSN

—

Svazek periodika

91

Číslo periodika v rámci svazku

—

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

50

Strana od-do

"S51"-"S100"

Kód UT WoS článku

000289374900007

EID výsledku v databázi Scopus

—