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2019
Daniel, Yvonne, Elion, Jacques 
ORCID: 0000-0002-8407-1783, Allaf, Bichr, Badens, Catherine, Bouva, Marelle J., Brincat, Ian, Cela, Elena, Coppinger, Cathy, de Montalembert, Mariane, Gulbis, Beatrice, Henthorn, Joan, Ketelslegers, Olivier, McMahon, Corrina, Streetly, Allison, Colombatti, Raffaella and Lobitz, Stephan ORCID: 0000-0001-5398-0610
(2019).
Newborn Screening for Sickle Cell Disease in Europe.
Int. J. Neonatal Screen., 5 (1).
BASEL:
MDPI.
ISSN 2409-515X
2018
Lobitz, Stephan ORCID: 0000-0001-5398-0610, Telfer, Paul, Cela, Elena, Allaf, Bichr, Angastiniotis, Michael, Backman Johansson, Carolina, Badens, Catherine, Bento, Celeste ORCID: 0000-0003-1080-411X, Bouva, Marelle J., Canatan, Duran, Charlton, Matthew, Coppinger, Cathy, Daniel, Yvonne, de Montalembert, Marianne, Ducoroy, Patrick, Dulin, Elena, Fingerhut, Ralph, Froemmel, Claudia, Garcia-Morin, Marina, Gulbis, Beatrice, Holtkamp, Ute, Inusa, Baba, James, John, Kleanthous, Marina, Klein, Jeannette, Kunz, Joachim B., Langabeer, Lisa, Lapoumeroulie, Claudine, Marcao, Ana, Marin Soria, Jose L., McMahon, Corrina, Ohene-Frempong, Kwaku, Perini, Jean-Marc, Piel, Frederic B., Russo, Giovanna ORCID: 0000-0001-9369-7473, Sainati, Laura, Schmugge, Markus, Streetly, Allison, Tshilolo, Leon, Turner, Charles, Venturelli, Donatella, Vilarinho, Laura ORCID: 0000-0001-6186-779X, Yahyaoui, Rachel, Elion, Jacques ORCID: 0000-0002-8407-1783 and Colombatti, Raffaella ORCID: 0000-0001-9797-0457
(2018).
Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference.
Br. J. Haematol., 183 (4).
S. 648 - 661.
HOBOKEN:
WILEY.
ISSN 1365-2141
2016
Lemke, Johannes R., Geider, Kirsten, Helbig, Katherine L., Heyne, Henrike O., Schutz, Hannah, Hentschel, Julia, Courage, Carolina, Depienne, Christel, Nava, Caroline ORCID: 0000-0003-1272-0518, Heron, Delphine, Moller, Rikke S., Hjalgrim, Helle, Lal, Dennis, Neubauer, Bernd A., Nurnberg, Peter, Thiele, Holger, Kurlemann, Gerhard, Arnold, Georgianne L., Bhambhani, Vikas, Bartholdi, Deborah, Pedurupillay, Christeen Ramane J., Misceo, Doriana, Frengen, Eirik ORCID: 0000-0002-8387-2247, Stromme, Petter, Dlugos, Dennis J., Doherty, Emily S., Bijlsma, Emilia K., Ruivenkamp, Claudia A., Hoffer, Mariette J. V., Goldstein, Amy, Rajan, Deepa S., Narayanan, Vinodh ORCID: 0000-0002-0658-3847, Ramsey, Keri, Belnap, Newell, Schrauwen, Isabelle ORCID: 0000-0001-7310-6082, Richholt, Ryan, Koeleman, Bobby P. C., Sa, Joaquim, Mendonca, Carla ORCID: 0000-0001-9926-0598, de Kovel, Carolien G. F., Weckhuysen, Sarah ORCID: 0000-0003-2878-1147, Hardies, Katia, De Jonghe, Peter, De Meirleir, Linda, Milh, Mathieu, Badens, Catherine ORCID: 0000-0001-9024-310X, Lebrun, Marine, Busa, Tiffany, Francannet, Christine, Piton, Amelie, Riesch, Erik, Biskup, Saskia, Vogt, Heinrich, Dorn, Thomas, Helbig, Ingo ORCID: 0000-0001-8486-0558, Michaud, Jacques L., Laube, Bodo and Syrbe, Steffen
(2016).
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy.
Neurology, 86 (23).
S. 2171 - 2179.
PHILADELPHIA:
LIPPINCOTT WILLIAMS & WILKINS.
ISSN 1526-632X