The European Joint Programme on Rare Diseases (EJP RD) is glad to announce that the last round for the Research Mobility Fellowships funding opportunity will open on October, 3rd, 2022. The call aims to support PhD students, postdocs, and medical doctors in training to undertake scientific visits fostering specialist research training outside their …
Author Archives: VASCERN Coordination
The ERN Research Training Workshops funding opportunity is now open for applications until October 1st. The goal of the workshops is to train researchers and clinicians affiliated to ERN- Full Members or – Affiliated Partners in relevant topics on research in rare diseases. Training themes may include innovative research methodologies, diagnostic research topics, interdisciplinary treatment approaches, such as gene therapy and transplantation, …
Two webinar videos have just been released on the VASCERN Youtube channel titled The A-Z of Aortic Syndrome in Marfan syndrome and Before and After Aortic Surgery: Q&A for Marfan Patients. These videos are recordings of an informative webinar on Aortic surgery in Marfan syndrome (and other HTADs) held on …
A new collaborative research paper titled Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN) was recently published in the European Journal of Medical Genetics as part of the VASCERN Special Issue. It is co-authored by members and affiliated partners of the VASCERN Medium Sized Arteries Working …
The Bring Your Own Omics Data (BYOOD) workshop (17th-18th November 2022) by EJ PRD is aiming to help you to optimize and integrate your omics data, initiate network analysis, and continue collaborations with the data analysis team. In order to help them further understand what your needs on data analysis are, and to adapt the workshop to them please complete …
In our first VASCERN Exchange Program interview, we are thrilled to interview Dr. Ruben Hermann from the CHU de Lyon HCL, GH Est-Hôpital Femme Mère Enfant in Lyon, France. Dr. Ruben Hermann is a member of the Hereditary Haemorrhagic Telangiectasia Working Group (HHT-WG). In this article, he shares what were …
EJP RD is delighted to announce the launch on June 30th, 2022 of the Innovation Management Toolbox (IMT), a free-to-use and curated reference library of resources in rare disease translational medicine that will provide investigators with self-help resources specific to their needs. The database will be maintained actively! Learn about the IMT: https://www.ejprarediseases.org/innovation-management-toolbox/Access the IMT: https://imt.ejprarediseases.org/
IRDiRC is pleased to announce that the IRDiRC‘s Rare Diseases Research Initiatives State of Play 2019-2021 Report will be published on Tuesday, 05 July 2022. This report is based on scientific articles and press releases published between 2019 and 2021; it seeks to inform stakeholders and the rare diseases community about the developments and observed trends in the field …
The webinar on “Composite endpoints including patient relevant endpoints (Quality of Life)” is now available here In this webinar you will learn about: The procedures to combine multiple endpoints and its limitations The properties and the flexibility of the class of generalized pairwise comparison tests The potential advantages and disadvantages …