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Anna Kole

European Organisation for Rare Diseases

10

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248

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E-Health & Innovation to Overcome Barriers in Neuromuscular Diseases. Report from the 1st eNMD Congress: Nice, France, March 22-23, 2019

2021 Journal of neuromuscular diseases
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Improving the informed consent process in international collaborative rare disease research: effective consent for effective research

2016 European Journal of Human Genetics
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‘You should at least ask’. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research

2016 European Journal of Human Genetics
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Current trends in biobanking for rare diseases: a review [Corrigendum]

2015
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International Charter of principles for sharing bio-specimens and data

2015 European Journal of Human Genetics
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TREAT-NMD (translational research in Europe, assessment and treatment for neuromuscular disorders)

2015 Neuromuscular Disorders
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Current trends in biobanking for rare diseases: a review

2014
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Setting up strategies: patient inclusion in biobank and genomics research in Europe

2014 Orphanet Journal of Rare Diseases
- Pauline McCormack
- Anna Kole
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The added value of centres of expertise for rare disease patients in Europe

2010 Orphanet Journal of Rare Diseases
- Anna Kole
- Yann Le Cam
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Rare Diseases Social Epidemiology: Analysis of Inequalities

2010 Advances in Experimental Medicine and Biology
- Anna Kole
- François Faurisson
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Citations (41)