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 Multi-level consistent changes of the ECM pathway identified in a typical keratoconus twin’s family by multi-omics analysis Xiao-dan Hao, Xiu-nian Chen, Yang-yang Zhang, Peng Chen, Chao Wei, Wei-yun Shi and Hua Gao Orphanet Journal of Rare Diseases 2020, 15:227 | Published on: 31 August 2020 Full Text | PDF RESEARCH Clinical profiles and risk factors of 7-day and 30-day mortality among 160 pediatric patients with hemophagocytic lymphohistiocytosis Xun Li, Haipeng Yan, Xinping Zhang, Jiaotian Huang, Shi-Ting Xiang, Zhenya Yao, Ping Zang, Desheng Zhu, Zhenghui Xiao and Xiulan Lu Orphanet Journal of Rare Diseases 2020, 15:229 | Published on: 31 August 2020 Full Text | PDF POSITION STATEMENT Providing high-quality care remotely to patients with rare bone diseases during COVID-19 pandemic E. Brizola, G. Adami, G. I. Baroncelli, M. F. Bedeschi, P. Berardi, S. Boero, M. L. Brandi, L. Casareto, E. Castagnola, P. Fraschini, D. Gatti, S. Giannini, M. V. Gonfiantini, V. Landoni, A. Magrelli, G. Mantovani… Orphanet Journal of Rare Diseases 2020, 15:228 | Published on: 31 August 2020 Full Text | PDF RESEARCH Participation in patient support forums may put rare disease patient data at risk of re-identification James Gow, Colin Moffatt and Jamie Blackport Orphanet Journal of Rare Diseases 2020, 15:226 | Published on: 31 August 2020 Full Text | PDF

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