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Adopting Quality Criteria for Websites Providing Medical Information About Rare Diseases

scientific article published on 25 August 2016

Concepts for the return of secondary genetic findings in medical diagnostics and research

artículo científico publicado en 2015

Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study.

artículo científico publicado en 2018

Criteria for fairly allocating scarce health-care resources to genetic tests: which matter most?

artículo científico publicado en 2013

Expression of a Y-located human proto-oncogene TSPY in a transgenic mouse model of prostate cancer.

artículo científico publicado en 2014

Long term follow up of patients after allogeneic stem cell transplantation and transfusion of HSV-TK transduced T-cells.

artículo científico publicado en 2015

Metadata Correction: Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study

scientific article published on 19 September 2018

New EuroGentest/ESHG guidelines and a new clinical utility gene card format for NGS-based testing

artículo científico publicado en 2015

Patient compliance based on genetic medicine: a literature review.

artículo científico publicado en 2013

Se-atlas-cartographic representation of experts for rare diseases.

artículo científico publicado en 2014

The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the

artículo científico

The future of Clinical Utility Gene Cards in the context of next-generation sequencing diagnostic panels.

artículo científico publicado en 2014

Value judgments for priority setting criteria in genetic testing: a discrete choice experiment.

artículo científico publicado en 2014

Vision and challenges of a cartographic representation of expert medical centres for rare diseases

artículo científico publicado en 2014

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