How to improve specific databases for clinical data in rare diseases? The example of hereditary haemorrhagic telangiectasia

16/11/2018

Artículos

Impact of measures to enhance the value of observational surveys in rare diseases: the Fabry Outcome Survey (FOS)

16/11/2018

Artículos

Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function

16/11/2018

Artículos

Innovative work behavior in healthcare: the benefit of operational guidelines in the treatment of rare diseases

16/11/2018

Artículos

Integrating medical and genomic data: a successful example for rare diseases

16/11/2018

Artículos

Health technologies for rare diseases: does conventional HTA still apply?

16/11/2018

Artículos

Hepatocanalicular transport defects: pathophysiologic mechanisms of rare diseases

16/11/2018

Artículos

Histamine: an undercover agent in multiple rare diseases?

16/11/2018

Artículos

How did uncommon disorders become ‘rare diseases’? History of a boundary object

16/11/2018

Artículos

How do patients with rare diseases experience the medical encounter? Exploring role behavior and its impact on patient-physician interaction

16/11/2018

Artículos