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 Less invasive treatment of sleep-disordered breathing in children with syndromic craniosynostosis Silvia Müller-Hagedorn, Cornelia Wiechers, Jörg Arand, Wolfgang Buchenau, Margit Bacher, Michael Krimmel, Siegmar Reinert and Christian F. Poets Orphanet Journal of Rare Diseases 2018, 13:63 | Published on: 23 April 2018 Full Text | PDF RESEARCH Gastro-oesophageal reflux - an important causative factor of severe tooth wear in Prader-Willi syndrome? Ronnaug Saeves, Finn Strøm, Leiv Sandvik and Hilde Nordgarden Orphanet Journal of Rare Diseases 2018, 13:64 | Published on: 23 April 2018 Full Text | PDF RESEARCH Serial MRIs provide novel insight into natural history of optic pathway gliomas in patients with neurofibromatosis 1 Laura Sellmer, Said Farschtschi, Marco Marangoni, Manraj K. S. Heran, Patricia Birch, Ralph Wenzel, Victor-Felix Mautner and Jan M. Friedman Orphanet Journal of Rare Diseases 2018, 13:62 | Published on: 23 April 2018 Full Text | PDF REVIEW Patient reported outcome measures in rare diseases: a narrative review Anita Slade, Fatima Isa, Derek Kyte, Tanya Pankhurst, Larissa Kerecuk, James Ferguson, Graham Lipkin and Melanie Calvert Orphanet Journal of Rare Diseases 2018, 13:61 | Published on: 23 April 2018 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

© 2018 BioMed Central Limited unless otherwise stated. Part of Springer Nature.