EJP RD workshop – The Blood-Brain Barrier: current research and novel therapeutic crossing approaches
Padua University hosts a scientific workshop exploring blood-brain barrier research and novel therapeutic strategies in rare diseases.
Patient representatives for Smith-Lemli-Opitz syndrome are looking for European families
A new research project explores Smith-Lemli-Opitz syndrome’s lifelong impact, inviting European families to share their experiences.
Rare disease education in Europe – read the new publication
Leading experts publish a position paper highlighting the urgent need for improved rare disease education across European healthcare.
Rare disease education in Europe – read the new publication Read More »
MetabERN Board meeting in Prague, 13-15 October 2022
The MetabERN Board reunites in Prague for its first face-to-face meeting since the pandemic, discussing key developments in rare diseases.
MetabERN Board meeting in Prague, 13-15 October 2022 Read More »
EJP Research Mobility Fellowship is now open
Research fellowship opportunity offers international training stays for PhD students, postdocs and medical doctors in rare disease research.
EJP Research Mobility Fellowship is now open Read More »
First Italian National Meeting on Rare Inherited Metabolic Diseases in Adults
A landmark national meeting in Udine addresses the growing challenges of managing inherited metabolic diseases in the adult population.
First Italian National Meeting on Rare Inherited Metabolic Diseases in Adults Read More »
IRDiRC Diagnostic Scientific Committee Nomination Call
The International Rare Diseases Research Consortium invites experts to join its Diagnostic Committee for advancing rare disease research.
IRDiRC Diagnostic Scientific Committee Nomination Call Read More »
Treatable neurometabolic diseases – Recordati Rare Diseases Foundation course 6-8 October 2022
Medical experts gather in Buenos Aires to discuss treatment advances and management strategies for inherited neurometabolic disorders.
Innovation Bootcamp in Rare Diseases (IBRD2022) congress
Brussels hosts the third Innovation Bootcamp exploring key challenges in rare disease diagnosis, treatment and drug development.
Innovation Bootcamp in Rare Diseases (IBRD2022) congress Read More »
International Neonatal Screening Day
June 28 marks the International Neonatal Screening Day, promoting early detection and treatment of rare conditions in newborns.
International Neonatal Screening Day Read More »
SSIEM Annual Symposium 2022
The SSIEM Annual Symposium 2022 will focus on metabolism and genetics, fostering discussions and networking in Freiburg from 30 August to 2 September.
SSIEM Annual Symposium 2022 Read More »
Pregnancy and Family Planning in rare diseases: a survey for patients and clinicians
MetabERN’s European survey on pregnancy and family planning for rare disease patients and clinicians aims to improve healthcare standards.
Pregnancy and Family Planning in rare diseases: a survey for patients and clinicians Read More »
