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Prevalence of esophageal atresia among 18 international birth defects surveillance programs

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064190%3A_____%2F12%3A%230000316" target="_blank" >RIV/00064190:_____/12:#0000316 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1002/bdra.23067" target="_blank" >http://dx.doi.org/10.1002/bdra.23067</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/bdra.23067" target="_blank" >10.1002/bdra.23067</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Prevalence of esophageal atresia among 18 international birth defects surveillance programs

  • Original language description

    BACKGROUND: The prevalence of esophageal atresia (EA) has been shown to vary across different geographical settings. Investigation of geographical differences may provide an insight into the underlying etiology of EA. METHODS: The study population comprised infants diagnosed with EA during 1998 to 2007 from 18 of the 46 birth defects surveillance programs, members of the International Clearinghouse for Birth Defects Surveillance and Research. Total prevalence per 10,000 births for EA was defined as thetotal number of cases in live births, stillbirths, and elective termination of pregnancy for fetal anomaly (ETOPFA) divided by the total number of all births in the population. RESULTS: Among the participating programs, a total of 2943 cases of EA were diagnosed with an average prevalence of 2.44 (95% confidence interval [CI], 2.352.53) per 10,000 births, ranging between 1.77 and 3.68 per 10,000 births. Of all infants diagnosed with EA, 2761 (93.8%) were live births, 82 (2.8%) stillbirth

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FP - Other medical fields

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    N - Vyzkumna aktivita podporovana z neverejnych zdroju

Others

  • Publication year

    2012

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

  • ISSN

    1542-9768

  • e-ISSN

  • Volume of the periodical

    94

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

    893-899

  • UT code for WoS article

    000311234400005

  • EID of the result in the Scopus database