Molecular genetic testing for ultra rare diseases: models for translation from the research laboratory to the CLIA-certified diagnostic laboratory

16/11/2018

Artículos

National plans and strategies on rare diseases in Europe

16/11/2018

Artículos

National Registries of Rare Diseases in Europe: An Overview of the Current Situation and Experiences

16/11/2018

Artículos

Networking for rare diseases: a necessity for Europe

16/11/2018

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New and evolving rare diseases research programs at the National Institutes of Health

16/11/2018

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Management options for rare diseases in children and adolescents in Georgia (experience of the country with transitional economy)

16/11/2018

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Meeting summary: Ethical aspects of whole exome and whole genome sequencing studies (WES/WGS) in rare diseases, Tel Aviv, Israel, January 2013

16/11/2018

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Methodological challenges in monitoring new treatments for rare diseases: lessons from the cryopyrin-associated periodic syndrome registry

16/11/2018

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Methodology of clinical research in rare diseases: development of a research program in juvenile neuronal ceroid lipofuscinosis (JNCL) via creation of a patient registry and collaboration with patient advocates

16/11/2018

Artículos

Methodology of clinical trials for rare diseases

16/11/2018

Artículos