Orphanet Journal of Rare Diseases is an open access, online journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs.
Editor-in-Chief
- Ségolène Aymé, Hopital Broussais, INSERM
Society affiliations
The official journal of Orphanet, the portal for rare diseases and orphan drugs
Letter to the Editor
Lougaris V, Salpietro V, Cutrupi M, Baronio M, Moratto D, Pizzino MR, Mankad K, Briuglia S et al.Orphanet Journal of Rare Diseases 2016, 11:3 (13 January 2016)
Research
Pinto D, Martin D and Chenhall ROrphanet Journal of Rare Diseases 2016, 11:2 (12 January 2016)
Letter to the Editor
Kuchinskaya E, Grigelioniene G, Hammarsjö A, Lee HR, Högberg L, Grigelionis G, Kim OH, Nishimura G et al.Orphanet Journal of Rare Diseases 2016, 11:1 (4 January 2016)
Research
Cassis L, Cortès-Saladelafont E, Molero-Luis M, Yubero D, González MJ, Herrero AO, Fons C, Jou C et al.Orphanet Journal of Rare Diseases 2015, 10:164 (30 December 2015)
Research
Boy N, Heringer J, Haege G, Glahn EM, Hoffmann GF, Garbade SF, Kölker S and Burgard POrphanet Journal of Rare Diseases 2015, 10:163 (22 December 2015)
Research
Pena MJ, Almeida MF, van Dam E, Ahring K, Bélanger-Quintana A, Dokoupil K, Gokmen-Ozel H, Lammardo AM et al.Orphanet Journal of Rare Diseases 2015, 10:162 (22 December 2015)
Letter to the Editor
Dooms MMOrphanet Journal of Rare Diseases 2015, 10:161 (21 December 2015)
Research
Abel LA, Walterfang M, Stainer MJ, Bowman EA and Velakoulis DOrphanet Journal of Rare Diseases 2015, 10:160 (21 December 2015)
Letter to the Editor
Komarow HD, Sokolic R, Hershfield MS, Kohn DB, Young M, Metcalfe DD and Candotti FOrphanet Journal of Rare Diseases 2015, 10:159 (18 December 2015)
Research
Jeannesson-Thivisol E, Feillet F, Chéry C, Perrin P, Battaglia-Hsu SF, Herbeth B, Cano A, Barth M et al.Orphanet Journal of Rare Diseases 2015, 10:158 (15 December 2015
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