Original language | English |
---|---|
Article number | 119 |
Number of pages | 9 |
Journal | Orphanet Journal of Rare Diseases |
Volume | 14 |
DOIs | |
Publication status | Published - 29 May 2019 |
Keywords
- European reference Centres
- Hereditary metabolic diseases
- Medical research activity
- Multidisciplinary research
- RARE DISEASES
- REGISTRIES
- BIOBANKS
Access to Document
Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver
}
Research activity and capability in the European reference network MetabERN. / Heard, Jean-Michel; Bellettato, Cinzia; van Lingen, Corine; Scarpa, Maurizio; Debray, Francois-Guillaume; Nassogne, Marie-Cecile; van Coster, Rudy; De Meirleir, Linda; Eyskens, Francois; Morava, Eva; Baric, Ivo; Kozich, Viktor; Lund, Allan Meldgaard; Germain, Dominique; Belmatoug, Nadia; Guffon, Nathalie; Labrune, Philippe; Gouya, Laurent; De Lonlay, Pascale; Schiff, Manuel; Dobbelaere, Dries; Chabrol, Brigitte; Ploeckinger, Ursula; Das, Anihb Martin; Scarpa, Maurizio; Spiekerkoetter, Ute; Rutsch, Frank; Mohnike, Klaus; Hahn, Andreas; Kolker, Stefan; Ullrich, Kurt; Hennermann, Julia; Balogh, Istvan; Bembi, Bruno; Donati, Maria Alice; Gasperini, Serena; Parenti, Giancarlo; Salviati, Alessandro; Vici, Carlo-Dionisi; Di Rocco, Maja; Cefalo, Graziella; Burlina, Alberto; Ceccarini, Giovanni; Federico, Antonio; Van der Ploeg, Ans; Rubio-Gozalbo, Maria-Estela; Van Spronsen, Francian; Visser, Gepke; Bosch, Annet; Tangeraas, Trine; MetabERN collaboration group.
In: Orphanet Journal of Rare Diseases, Vol. 14, 119, 29.05.2019.Research output: Contribution to journal › Article › Academic › peer-review
TY - JOUR
T1 - Research activity and capability in the European reference network MetabERN
AU - Heard, Jean-Michel
AU - Bellettato, Cinzia
AU - van Lingen, Corine
AU - Scarpa, Maurizio
AU - Debray, Francois-Guillaume
AU - Nassogne, Marie-Cecile
AU - van Coster, Rudy
AU - De Meirleir, Linda
AU - Eyskens, Francois
AU - Morava, Eva
AU - Baric, Ivo
AU - Kozich, Viktor
AU - Lund, Allan Meldgaard
AU - Germain, Dominique
AU - Belmatoug, Nadia
AU - Guffon, Nathalie
AU - Labrune, Philippe
AU - Gouya, Laurent
AU - De Lonlay, Pascale
AU - Schiff, Manuel
AU - Dobbelaere, Dries
AU - Chabrol, Brigitte
AU - Ploeckinger, Ursula
AU - Das, Anihb Martin
AU - Scarpa, Maurizio
AU - Spiekerkoetter, Ute
AU - Rutsch, Frank
AU - Mohnike, Klaus
AU - Hahn, Andreas
AU - Kolker, Stefan
AU - Ullrich, Kurt
AU - Hennermann, Julia
AU - Balogh, Istvan
AU - Bembi, Bruno
AU - Donati, Maria Alice
AU - Gasperini, Serena
AU - Parenti, Giancarlo
AU - Salviati, Alessandro
AU - Vici, Carlo-Dionisi
AU - Di Rocco, Maja
AU - Cefalo, Graziella
AU - Burlina, Alberto
AU - Ceccarini, Giovanni
AU - Federico, Antonio
AU - Van der Ploeg, Ans
AU - Rubio-Gozalbo, Maria-Estela
AU - Van Spronsen, Francian
AU - Visser, Gepke
AU - Bosch, Annet
AU - Tangeraas, Trine
AU - MetabERN collaboration group
PY - 2019/5/29
Y1 - 2019/5/29
KW - European reference Centres
KW - Hereditary metabolic diseases
KW - Medical research activity
KW - Multidisciplinary research
KW - RARE DISEASES
KW - REGISTRIES
KW - BIOBANKS
U2 - 10.1186/s13023-019-1091-8
DO - 10.1186/s13023-019-1091-8
M3 - Article
C2 - 31142374
VL - 14
JO - Orphanet Journal of Rare Diseases
JF - Orphanet Journal of Rare Diseases
SN - 1750-1172
M1 - 119
ER -