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Category Archives: News

Duchenne Data Foundation   →  News
Author By Nicoletta MadiaPosted on 15/02/202115/02/2022

Duchenne Emergency and Capacity Building Program

Duchenne Data Foundation and the World Duchenne Organization start the Duchenne Emergency and Capacity Building Program FIRST A...
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Author By Elvina SakellariouPosted on 03/02/202115/02/2022

Job Position: Data steward

About DDF  Duchenne Data Foundation is a worldwide collaboration in order to enhance the understanding of the course of Du...
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Author By Suzie-Ann BakkerPosted on 09/12/202015/02/2022

DDF successfully concludes third Duchenne Patient Academy

International training for neuromuscular patient advocates ATHENS, Dec. 9, 2020 /Duchenne Data Foundation/ -- Duchenne Patient...
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Author By Suzie-Ann BakkerPosted on 26/10/202015/02/2022

Apply now for Duchenne Patient Academy 2020

Duchenne Patient Academy works in partnership with leading DMD patient organisations to set a strong patient advocacy base for pat...
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Author By Suzie-Ann BakkerPosted on 07/09/202015/02/2022

DDF supports World Duchenne Awareness Day

Today is World Duchenne Awareness Day. As of each year on September 7, the world raises global awareness on Duchenne and Becker mu...
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Author By Sally HofmeisterPosted on 11/08/202015/02/2022

Report: 5th Duchenne CAB Meeting

The Duchenne CAB held its 5th meeting from 13 – 15 May 2020. Due to the COVID-19 pandemic the meetings had to be held virtu...
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Author By Suzie-Ann BakkerPosted on 29/01/202015/02/2022

Large international project to study dystrophin in the brain in DMD/BMD launched

The BIND project is the first project of this scale to improve characterisation of brain involvement in Duchenne an...
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Author By Sally HofmeisterPosted on 15/12/201915/02/2022

Report: 4th Duchenne CAB Meeting

The Duchenne CAB held its 4thmeeting from 23 – 26 October in Amsterdam. This time we were able to welcome four companies, one of...
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Author By Suzie-Ann BakkerPosted on 11/12/201915/02/2022

3rd Duchenne Patient Academy trains 80 patient advocates from 37 countries

Three years ago, the first Duchenne Patient Academy (DPA) was launched in Athens, Greece. This global patient advocacy initiative...
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Author By Suzie-Ann BakkerPosted on 19/10/201915/02/2022

Open call for Duchenne Advocates

Over the past years, the Duchenne world has been changing due to a fast evolving research and regulatory landscape. For this, the...
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Categories

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  • ERDERA 1
  • EU Projects 8
  • News 32
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  • Uncategorized 1
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Recent Posts

  • Applications now open for Duchenne Patient Academy 202404/11/2024
  • Be Part of a Major Milestone in Rare Disease Research: Join ERDERA’s Launch Event!18/10/2024
  • BIND Project secures funding to continue genotype phenotype correlation of DMD/BMD brain18/09/2024
  • Launch of the ERDERA partnership16/09/2024
  • iMM Joins the MAGIC Consortium to Advance Research on Muscular Dystrophies07/06/2024

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Duchenne Data Foundation
We bring together fragmented data pieces of the Duchenne and Becker muscular dystrophy (DMD/BMD) world and test innovative solutions, scaling them to make a global impact

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