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Burden of non-communicable disease studies in Europe: a systematic review of data sources and methodological choices

Mortality data were mainly derived (49%) from vital statistics. Morbidity data were frequently (40%) drawn from routine administrative and survey datasets, including disease registries and hospital discharge ...

Unravelling data for rapid evidence-based response to COVID-19: a summary of the unCoVer protocol

surveillance and screening data, and registries with over 1 900 000 COVID-19 cases across Europe, with continuous updates. These heterogeneous datasets will be described, harmonised and integrated into ...

The non-fatal burden of cancer in Belgium, 2004–2019: a nationwide registry-based study

registry data and international disease models. We developed a microsimulation model to translate incidence- into prevalence-based estimates, and used expert elicitation to integrate the long-term impact of ...

Validity of self-reported air pollution annoyance to assess long-term exposure to air pollutants in Belgium

survey participants through Geographical Information Systems (GIS). However, obtaining georeferenced address data from national registries requires a long and cumbersome administrative procedure, since ...

Incidence of SARS-CoV-2 in people with cystic fibrosis in Europe between February and June 2020.

 (pwCF). METHODS: We used the 38-country European Cystic Fibrosis Society Patient Registry (ECFSPR) to collect case data about pwCF and SARS-CoV-2 infection. RESULTS: Up to 30 June 2020, 16 countries ...

Annual report Belgian Cystic Fibrosis Registry 2019

Publication Type: Sci. report, recommendat°, guidance doc., directive, monograph Authors: Wanyama, Simeon; Daneau, Géraldine; Dupont, Lieven Source: Sciensano, Brussels, Belgium, p.104 (2021) Accession Number: D/2020/14.440/85 Keywords: annual report Cyst ...

Conducting national burden of disease studies in small countries in Europe– a feasible challenge?

expertise, and engage with countries and institutions that have long-standing experience with BoD assessment. Conclusion Apart from mortality registries, adequate health data sources, notably for cancer, are ...

Belgian NMD registry

neuromuscular diseases registry BNMDR Abstract: This presentation gives a brief overview of the Belgian neuromuscular diseases registry and includes information on the set up, overall numbers, projects ...

Annual report Belgian Cystic Fibrosis Registry 2018

of the registry data will provide readers with information on various aspects of CF and continue to provide an important tool for monitoring the patient’s quality of care and trends.     Since its ...

The Belgian Cystic Fibrosis Registry- Facts and highlights 2018

https://www.sciensano.be/en/biblio/belgian-cystic-fibrosis-registry-facts-and-hi... File:  Version:  Published Full text access:  Public Access Full text language:  English Category:  F21 FOS Classification:  3.02 Clinical medicine ...

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