Informed consent for neonatal trials: practical points to consider and a check list by Donato Bonifazi, Evelyne Jacqz-Aigrain, Christine Kubiak, Mariette H E Driessens, Beate Aurich, Eric Vermeulen, Valéry Elie

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Toward Personalized Care and Patient Empowerment and Perspectives on a Personal Health Record in Hemophilia Care: Qualitative Interview Study by Martijn R Brands, Lotte Haverman, Jelmer J Muis, Mariëtte H E Driessens, Stephan Meijer, Felix J M van der Meer, Marianne de Jong, Johanna G van der Bom, Marjon H Cnossen, Karin Fijnvandraat, Samantha C Gouw

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Socioeconomic participation of persons with hemophilia: Results from the sixth hemophilia in the Netherlands study by Erna C. van Balen, Shermarke Hassan, Cees Smit, Mariette H. E. Driessens, Erik A. M. Beckers, Michiel Coppens, Jeroen C. Eikenboom, Hélène L. Hooimeijer, Frank W. G. Leebeek, Evelien P. Mauser‐Bunschoten, Lize F. D. van Vulpen, Saskia E. M. Schols, Frits R. Rosendaal, Johanna G. van der Bom, Samantha C. Gouw

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