martes, 1 de septiembre de 2020

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page



New Articles For BioMed Central:

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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