Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases RESEARCH Sick leave, disability, and mortality in acute hepatic porphyria: a nationwide cohort study Carl Michael Baravelli, Aasne Karine Aarsand, Sverre Sandberg and Mette Christophersen Tollånes Orphanet Journal of Rare Diseases 2020, 15:56 | Published on: 21 February 2020 Full Text | PDF RESEARCH Equivocal expression of emotions in children with Prader-Willi syndrome: what are the consequences for emotional abilities and social adjustment? Nawelle Famelart, Gwenaelle Diene, Sophie Çabal-Berthoumieu, Mélanie Glattard, Catherine Molinas, Michèle Guidetti and Maithe Tauber Orphanet Journal of Rare Diseases 2020, 15:55 | Published on: 21 February 2020 Full Text | PDF RESEARCH Lack of knowledge and misperceptions about thalassaemia among college students in Bangladesh: a cross-sectional baseline study Mohammad Sorowar Hossain, Md. Mahbub Hasan, Enayetur Raheem, Muhammad Sougatul Islam, Abdullah Al Mosabbir, Mary Petrou, Paul Telfer and Mahbubul H. Siddiqee Orphanet Journal of Rare Diseases 2020, 15:54 | Published on: 21 February 2020 Full Text | PDF

Follow BMC on: For further information or enquiries please use our contact page details. BMC respects your privacy and does not disclose, sell or rent your personal information to any non-affliated third parties with your consent. Privacy policy. BioMed Central Ltd The Campus, 4 Crinan Street, London, N1 9XW, United Kingdom

© 2020 BioMed Central Limited unless otherwise stated. Part of Springer Nature.