New Articles From Orphanet Journal of Rare Diseases

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases RESEARCH Cognitive impairment profile in adult patients with Niemann pick type C disease Camille Heitz, Stéphane Epelbaum and Yann Nadjar Orphanet Journal of Rare Diseases 2017, 12:166 | Published on: 18 October 2017 Full Text | PDF RESEARCH A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry Riccardo Papa, Matteo Doglio, Helen J. Lachmann, Seza Ozen, Joost Frenkel, Anna Simon, Bénédicte Neven, Jasmin Kuemmerle-Deschner, Huri Ozgodan, Roberta Caorsi, Silvia Federici, Martina Finetti, Maria Trachana, Jurgen Brunner, Liliana Bezrodnik, Mari Carmen Pinedo Gago… Orphanet Journal of Rare Diseases 2017, 12:167 | Published on: 18 October 2017 Full Text | PDF

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