Search results - 17 results

Rapport d'activité Orphanet Belgium 2020

D/2021/14.440/35 Keywords: Database Orphanet Rare diseases Health Topics:  Orphan diseases Weesziekten Maladies orphelines Service:  Épidémiologie et santé publique Epidemiologie en volksgezondheid Epidemiology and ...

Orphanet Belgium activiteitenrapport 2020

D/2021/14.440/36 Keywords: Database Orphanet Rare diseases Health Topics:  Orphan diseases Weesziekten Maladies orphelines Maladies rares Zeldzame ziekten Service:  Épidémiologie et santé publique Epidemiologie en ...

Orphanet Belgium activity report 2020

D/2021/14.440/37 Keywords: Database Orphanet Rare diseases Health Topics:  Rare diseases Maladies rares Zeldzame ziekten Service:  Épidémiologie et santé publique Epidemiologie en volksgezondheid Epidemiology and ...

Orphanet Belgium activiteitenrapport 2017-2019

Keywords: Database Orphanet Rare diseases Health Topics:  Orphan diseases Weesziekten Maladies orphelines Surveillance de la santé et des maladies Ziekten en gezondheid in kaart brengen Service:  ...

Orphanet Belgium activity report 2017-2019

D/2020/14.440/99 Keywords: Rare diseases & Orphanet & database Health Topics:  Orphan diseases Weesziekten Maladies orphelines Service:  Épidémiologie et santé publique Epidemiologie en volksgezondheid ...

Rapport d'activité Orphanet Belgium 2017-2019

D/2020/14.440/97 Keywords: Orphanet & maladies rares & base de données Health Topics:  Rare diseases Maladies rares Zeldzame ziekten Service:  Épidémiologie et santé publique Epidemiologie en volksgezondheid ...

Orphanet Report Series- Lijst van zeldzame ziekten en synoniemen

Publication Type: Sci. report, recommendat°, guidance doc., directive, monograph Authors: Kim Van Roey Source: p.213 (2020) Full text language:  Dutch Category:  E12 FOS Classification:  3.03 Health sciences ...

Orphanet vertaling: activiteitenrapport (2018-2019)

Publication Type: Sci. report, recommendat°, guidance doc., directive, monograph Authors: Van Roey, K; Swinnen, E; Doggen, K Source: p.17 (2019) Accession Number: D/2020/14.440/92; D/2020/14.440/94; D/2020/14.440/93 Manuscript versions:  File:  Version:  ...

Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease.

Miriam; Roxburgh, Richard; Schoser, Benedikt; Segovia, Sonia; Shatillo, Andriy; Thiele, Simone; Tournev, Ivailo; van Engelen, Baziel; Vohanka, Stanislav; Lochmüller, Hanns Source: Orphanet J Rare Dis, ...

What can the CF registry tell us about rare CFTR-mutations? A Belgian study.

Publication Type: Peer reviewed scientific article Authors: De Wachter, E; Muriel Thomas; Simeon Wanyama; Seneca, S; Malfroot, A Source: Orphanet J Rare Dis, Volume 12, Issue 1, p.142 (2017) ...

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