Category: A4R – Alliance4Rare
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A4R – Alliance4Rare
Biliary atresia: How do children live with this rare liver disease, and what is Alliance4Rare researching? Author Berit Hullmann, chairwoman of Leberkrankes Kind e.V., met with families and researchers. She…
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A4R – Alliance4Rare
University Hospital Tübingen Becomes New Site Partner of Research Initiative Alliance4Rare
A strong network grows even stronger: With support from the Wilfried and Martha Ensinger Foundation, University Hospital Tübingen can now become the fifth location in the Alliance4Rare network.
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A4R – Alliance4Rare
Clinician Scientists in Profile: Dr. Lara Lechner, Charité – Universitätsmedizin Berlin
Our Alliance4Rare research network not only invests in research programs but, through Clinician Scientist Programs, also fosters urgently needed scientific talent. Here, Dr. Lara Lechner/ Charité – Universitätsmedizin Berlin introduces…
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A4R – Alliance4Rare
Junior Clinician Scientist: Dr. Klara Brüning, Charité – Universitätsmedizin Berlin
The Alliance4Rare research network not only invests in research programs, but also in urgently needed young scientists through clinician/medical scientist programs. Here, Dr. Klara Brüning/ Charité - Universitätsmedizin Berlin introduces…
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A4R – Alliance4Rare
Shining a Spotlight on Childhood Dementia: New Clinician Scientist Professorship for Rare Diseases
Eva Luise and Horst Köhler Foundation and Else Kröner-Fresenius Foundation provide 1.1 million euros in funding for research and patient care…
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A4R – Alliance4Rare
Clinician Scientist: Dr. Julia Körholz, University Hospital Dresden
The Alliance4Rare research network not only invests in research projects, but also in urgently needed young scientists through clinician/medical scientist programs. Lern more about Dr. Julia Körholz, University Hospital Dresden,…
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A4R – Alliance4Rare
Spotlight on Rare Diseases: Alliance4Rare at the ‘Ein Herz für Kinder’ Fundraising Gala
On Saturday, December 7, 2024, we had the honor of joining the 'Ein Herz für Kinder' fundraising gala on ZDF. A heartfelt thank you to BILD hilft e.V. for the…
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A4R – Alliance4Rare
Alliance4Rare funding: Newborn genetic screening pilot project launched
Around five million people in Germany are living with rare, mostly genetic diseases. Many of these diseases could be diagnosed in newborn babies - but the diagnosis is often made…
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A4R – Alliance4Rare
Hope for children with rare immune disorders: Alliance4Rare funds innovative research
Children affected by rare immune disorders often suffer from severe chronic inflammation and autoimmune diseases that can severely limit their lives. But there is hope: funded by Alliance4Rare, the research…
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A4R – Alliance4Rare
Clinician Scientist: Dr. Steffen Köhne, Universitätsmedizin Göttingen
The Alliance4Rare research network not only invests in research programs, but also in urgently needed young scientists through clinician/medical scientist programs. Read more about Dr. Nina-Maria Wilpert, Charité - Universitätsmedizin…
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A4R – Alliance4Rare
Alliance4Rare call for proposals: Junior Clinician Scientists for Rare (JCS4Rare)
The Alliance4Rare offers Junior Clinician Scientists for Rare (JCS4Rare) a structured specialist training program that enables prospective pediatricians and human geneticists with a clearly recognizable scientific interest in rare diseases…
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A4R – Alliance4Rare
Two years Alliance4Rare: pioneering work for research into rare diseases
Research gives hope to the youngest: At the two-year anniversary of the Alliance4Rare research initiative, scientific director Prof. Dr. Annette Grüters-Kieslich reports on the successes, challenges and goals of the…