Funding for the best collaborative research initiative: extension of the deadline for the Share4Rare Call4Projects
In response to inquiries and requests from those interested in this year's project call, Share4Rare will grant funding to the best collaborative research initiative based on data reported by patientsRare Horizons episode 2 focuses on people living without a diagnosis
People need to name things. Naming is our way of creating some order in this chaotic world. Unfortunately, many people are not able to name their disease. In Europe, it takes an average of five yearsAn amino acid shows therapeutic potential in people with GRIN-related disorders
A pioneering clinical trial led by Dr Àngels Garcia-Cazorla from the Sant Joan de Déu Research Institute · Sant Joan de Déu Hospital has demonstrated that oral administration of the amino acid LShare4Rare will host a webinar on the 2024 research project call
Share4Rare aims to enhance research on rare diseases through collaborative knowledge generation. The platform provides researchers with a secure infrastructure to conduct their investigationsA study uncovers the connection between mutations in the GEMIN5 gene and Coenzyme Q10 deficiency
In science, things take time, but perseverance can eventually bear fruit. The results of this work, published in the European Journal of Human Genetics, began in 2004 with the study of a 12-year-oldRare Horizons, a new podcast focused on rare disease research
Education stands as a key pillar of Share4Rare. Thus, we are constantly working to provide the rare disease community with tools and resources to better understand the various research dimensions ofÚnicas SJD building construction begins in Barcelona, dedicated to rare disease care and research
The new building will rise 250 metres from the Sant Joan de Déu Hospital, situated between the municipalities of Barcelona and Esplugues de Llobregat (Barcelona province, Spain). Its main facade will4th Share4Rare Call4Projects to drive rare disease patient-driven research studies
Collaborative research into rare diseases stands as one of the cornerstones of Share4Rare. Year after year, we endeavour to foster the development of research projects in this field that focus on theNerea González — Affected by a mitochondrial disease and a member of AEPMI
Nerea González defines herself as a " Mito Warrior," a fighter who refuses to surrender to adversity. And she knows a lot about adversity. One of the conditions she suffers from is Coenzyme Q10New project to enhance the use of photonics and artificial intelligence in disease diagnosis
The BE-LIGHT project, funded by the Horizon Europe program of the European Union, aims to design novel instruments and clinical methods capable of obtaining images of tissues previously unattainable