Literature DB >> 11446615

European collaboration in research into rare diseases: experience of the European Neuromuscular Centre.

A Emery1, M Rutgers.   

Abstract

An understanding of the possible causes, prevention and treatment of rare, so-called 'orphan disease' requires collaboration in research between different centres with the sharing of information. In the case of neuromuscular disorders (such as muscular dystrophies or hereditary neuropathies) this has been achieved through European collaborative research encouraged and facilitated by the European Neuromuscular Centre (ENMC). The successful example of ENMC provides a model for the investigation of other rare 'orphan' disorders or even rare problems occurring in common disorders.

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Year:  2001        PMID: 11446615      PMCID: PMC4951906          DOI: 10.7861/clinmedicine.1-3-200

Source DB:  PubMed          Journal:  Clin Med (Lond)        ISSN: 1470-2118            Impact factor:   2.659


  1 in total

1.  Reduced miR-146a Promotes REG3A Expression and Macrophage Migration in Polymyositis and Dermatomyositis.

Authors:  Tingwang Jiang; Yuanlan Huang; Haohao Liu; Qiangwei Xu; Yanping Gong; Yao Chen; Xiaowei Hu; Zhijun Han; Mingzhu Gao
Journal:  Front Immunol       Date:  2020-02-21       Impact factor: 7.561

  1 in total

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